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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.
mRNA and Protein(s)
-
NM_001114600.3 → NP_001108072.1 SUZ RNA-binding domain-containing isoform 1
See identical proteins and their annotated locations for NP_001108072.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (1) encodes the longer isoform (1).
- Source sequence(s)
-
AB097046, AL358794, BC010631, DB501645
- Consensus CDS
-
CCDS44065.1
- UniProtKB/Swiss-Prot
- A8MXJ2, C9K0U0, Q7Z422, Q7Z424, Q8IVM2, Q8TBV3, Q9Y403
- UniProtKB/TrEMBL
- B4DNI1, E7ENW9
- Related
- ENSP00000383866.4, ENST00000401088.9
- Conserved Domains (2) summary
-
- pfam12752
Location:56 → 107
- SUZ; SUZ domain
- pfam12901
Location:119 → 151
- SUZ-C; SUZ-C motif
-
NM_001271869.2 → NP_001258798.1 SUZ RNA-binding domain-containing isoform 3
See identical proteins and their annotated locations for NP_001258798.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (3) uses an alternate in-frame splice site, compared to variant 1. The encoded isoform (3) is shorter than isoform 1.
- Source sequence(s)
-
AL358794, BC010631, DA010145
- Consensus CDS
-
CCDS60000.1
- UniProtKB/TrEMBL
- B4DNI1, E7ENW9
- Related
- ENSP00000419589.1, ENST00000471507.5
- Conserved Domains (2) summary
-
- pfam12752
Location:55 → 106
- SUZ; SUZ domain
- pfam12901
Location:118 → 150
- SUZ-C; SUZ-C motif
RNA
-
NR_073500.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (5) lacks two internal exons, compared to variant 1. This variant is represented as non-coding because it lacks a large portion of the coding region found in variant 1.
- Source sequence(s)
-
AK308787, AL358794, BC010631, DB501645
-
NR_073501.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (6) contains an alternate internal exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AL358794, BC010631, DA438597, DB501645
-
NR_073502.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (2) lacks an alternate internal exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AL358794, BC010631, BC023988
- Related
-
ENST00000401089.3
-
NR_073503.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (4) lacks an internal exon and uses an alternate splice site, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AB097044, AL358794, BC010631, DB501645
- Related
-
ENST00000492354.1
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_000001.11 Reference GRCh38.p14 Primary Assembly
- Range
-
16367242..16398145
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Reference GRCh38.p14 PATCHES
Genomic
-
NW_025791756.1 Reference GRCh38.p14 PATCHES
- Range
-
171377..202286
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060925.1 Alternate T2T-CHM13v2.0
- Range
-
15808777..15839678
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)