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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_001167830.2 → NP_001161302.1 transmembrane emp24 domain-containing protein 5 isoform 2 precursor
Status: VALIDATED
- Description
- Transcript Variant: This variant (2) includes an alternate exon that causes a frameshift in the 3' coding region, compared to variant 1. The resulting isoform (2) has a distinct and shorter C-terminus, compared to isoform 1.
- Source sequence(s)
-
AC126124, AL117354, CA314982
- Consensus CDS
-
CCDS53342.1
- UniProtKB/TrEMBL
-
B1AKT3
- Related
- ENSP00000418992.1, ENST00000479918.5
- Conserved Domains (1) summary
-
- pfam01105
Location:35 → 162
- EMP24_GP25L; emp24/gp25L/p24 family/GOLD
-
NM_001410825.1 → NP_001397754.1 transmembrane emp24 domain-containing protein 5 isoform 3 precursor
Status: VALIDATED
- Source sequence(s)
-
AC126124, AL117354
- Consensus CDS
-
CCDS91003.1
- UniProtKB/TrEMBL
-
M0R072
- Related
- ENSP00000471060.1, ENST00000370290.7
-
NM_016040.5 → NP_057124.3 transmembrane emp24 domain-containing protein 5 isoform 1 precursor
See identical proteins and their annotated locations for NP_057124.3
Status: VALIDATED
- Description
- Transcript Variant: This variant (1) encodes the longer isoform (1).
- Source sequence(s)
-
AI436590, AL117354, BC070051, CA314982
- Consensus CDS
-
CCDS743.1
- UniProtKB/Swiss-Prot
- B1AKT4, B2R703, D3DT38, Q96AX8, Q9Y3A6
- Related
- ENSP00000359305.3, ENST00000370282.8
- Conserved Domains (1) summary
-
- pfam01105
Location:35 → 222
- EMP24_GP25L; emp24/gp25L/p24 family/GOLD
RNA
-
NR_030761.2 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (3) includes an alternate internal exon, compared to variant 1. This variant is represented as non-coding because the use of the supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AC126124, AL117354, BX642274, CA314982
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
-
93149742..93180413 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060925.1 Alternate T2T-CHM13v2.0
- Range
-
92995327..93026003 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)