NEW
Try the new Transcript table
These reference sequences exist independently of genome builds. Explain
These reference sequences are curated independently of the genome
annotation cycle, so their versions may not match the RefSeq versions in the current
genome build. Identify version mismatches by comparing the version of the RefSeq in
this section to the one reported in Genomic regions,
transcripts, and products above.
Genomic
-
NG_047033.1 RefSeqGene
- Range
-
5052..14377
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
NM_001612.6 → NP_001603.1 acrosomal protein SP-10 isoform a precursor
See identical proteins and their annotated locations for NP_001603.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (1) represents the full length form of this gene, which encodes 265 aa. All other variants, as compared to this variant, lack one or two in-frame fragments in exons II and/or III.
- Source sequence(s)
-
AP001132, BC014588
- Consensus CDS
-
CCDS8460.1
- UniProtKB/Swiss-Prot
- P26436, Q53FF4
- UniProtKB/TrEMBL
-
B5BUP0
- Related
- ENSP00000432816.1, ENST00000533904.6
- Conserved Domains (2) summary
-
- PHA03169
Location:47 → 184
- PHA03169; hypothetical protein; Provisional
- cd00117
Location:188 → 264
- LU; Ly-6 antigen / uPA receptor -like domain; occurs singly in GPI-linked cell-surface glycoproteins (Ly-6 family,CD59, thymocyte B cell antigen, Sgp-2) or as three-fold repeated domain in urokinase-type plasminogen activator receptor. Topology of these ...
-
NM_020069.5 → NP_064454.1 acrosomal protein SP-10 isoform b precursor
See identical proteins and their annotated locations for NP_064454.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (2) lacks a 57 nt fragment in the 3'-terminus of the exon II, as compared to variant 1. Isoform b encoded by this variant is thus 19 aa shorter than isoform a encoded by variant 1.
- Source sequence(s)
-
AP001132, BC014588, DB446200, M82967
- Consensus CDS
-
CCDS44759.1
- UniProtKB/TrEMBL
-
B5BUP0
- Related
- ENSP00000317684.3, ENST00000315608.7
- Conserved Domains (1) summary
-
- cd00117
Location:169 → 245
- LU; Ly-6 antigen / uPA receptor -like domain; occurs singly in GPI-linked cell-surface glycoproteins (Ly-6 family,CD59, thymocyte B cell antigen, Sgp-2) or as three-fold repeated domain in urokinase-type plasminogen activator receptor. Topology of these ...
-
NM_020107.5 → NP_064492.1 acrosomal protein SP-10 isoform c precursor
See identical proteins and their annotated locations for NP_064492.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (3) lacks a 165 nt fragment within exon II, which results in 55 aa fewer in isoform c, as compared to isoform a encoded by variant 1.
- Source sequence(s)
-
AP001132, BC014588, BI826178, DB446200
- Consensus CDS
-
CCDS8461.1
- UniProtKB/Swiss-Prot
-
P26436
- Related
- ENSP00000433720.1, ENST00000530048.5
- Conserved Domains (1) summary
-
- cd00117
Location:133 → 209
- LU; Ly-6 antigen / uPA receptor -like domain; occurs singly in GPI-linked cell-surface glycoproteins (Ly-6 family,CD59, thymocyte B cell antigen, Sgp-2) or as three-fold repeated domain in urokinase-type plasminogen activator receptor. Topology of these ...
-
NM_020108.5 → NP_064493.1 acrosomal protein SP-10 isoform d precursor
See identical proteins and their annotated locations for NP_064493.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (4) lacks a 210 nt fragment in exon II, which results in 70 aa fewer in isoform d, as compared to isoform a encoded by variant 1.
- Source sequence(s)
-
AP001132, BC014588, BG720361
- Consensus CDS
-
CCDS44761.1
- UniProtKB/Swiss-Prot
-
P26436
- Related
- ENSP00000436819.1, ENST00000527795.1
- Conserved Domains (1) summary
-
- cd00117
Location:118 → 194
- LU; Ly-6 antigen / uPA receptor -like domain; occurs singly in GPI-linked cell-surface glycoproteins (Ly-6 family,CD59, thymocyte B cell antigen, Sgp-2) or as three-fold repeated domain in urokinase-type plasminogen activator receptor. Topology of these ...
The following sections contain reference sequences that belong to a
specific genome build. Explain
This section includes genomic Reference
Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as
RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate
assemblies. Model RNAs and proteins are also reported here.
Reference GRCh38.p14 Primary Assembly
Genomic
-
NC_000011.10 Reference GRCh38.p14 Primary Assembly
- Range
-
125671522..125680847 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060935.1 Alternate T2T-CHM13v2.0
- Range
-
125700163..125709487 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
The following Reference Sequences have been suppressed. Explain
These RefSeqs were suppressed for the
cited reason(s). Suppressed RefSeqs do not appear in BLAST databases, related
sequence links, or BLAST links (BLink), but may still be retrieved by clicking on
their accession.version below.
-
NM_020109.3: Suppressed sequence
- Description
- NM_020109.3: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.
-
NM_020110.3: Suppressed sequence
- Description
- NM_020110.3: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.
-
NM_020111.3: Suppressed sequence
- Description
- NM_020111.3: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.
-
NM_020112.3: Suppressed sequence
- Description
- NM_020112.3: This RefSeq was permanently suppressed because currently there is support for the transcript but not for the protein.
-
NM_020113.3: Suppressed sequence
- Description
- NM_020113.3: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.
-
NM_020114.3: Suppressed sequence
- Description
- NM_020114.3: This RefSeq was permanently suppressed because it contains the wrong CDS.
-
NM_020115.3: Suppressed sequence
- Description
- NM_020115.3: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.