Human (GRCh38.p14)
Description

chromosome 9 open reading frame 57 [Source:HGNC Symbol;Acc:HGNC:27037]

Location
About this transcript

This transcript has 4 exons, is annotated with 1 domain and feature, is associated with 9118 variant alleles and maps to 236 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000651200.2C9orf57-2041510139aaENSP00000498279.1
 
Protein coding
CCDS47980A0A494C0F4 NM_001128618.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS ALT2
ENST00000652156.1C9orf57-2051640139aaENSP00000498526.1
 
Protein coding
CCDS47980A0A494C0F4 -GENCODE basicAPPRIS ALT2
ENST00000377024.8C9orf57-2011495161aaENSP00000366223.3
 
Protein coding
Q5W0N0-1 -GENCODE basicAPPRIS P2TSL:1
ENST00000652752.1C9orf57-2061448118aaENSP00000498340.1
 
Protein coding
A0A494C027 -GENCODE basic
ENST00000424431.3C9orf57-2021297127aaENSP00000412956.2
 
Protein coding
Q5W0N0-2 -GENCODE basicTSL:1
ENST00000651121.1C9orf57-203153745aaENSP00000499189.1
 
Nonsense mediated decay
A0A494C1R2 --
ENST00000673779.1C9orf57-2071360No protein-
 
Protein coding CDS not defined
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Statistics

Exons: 4, Coding exons: 4, Transcript length: 1,297 bps, Translation length: 127 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q5W0N0

Transcript Support Level (TSL)

TSL:1

Version

ENST00000424431.3

Type

Protein coding

Annotation Method

Annotation produced by the Ensembl genebuild.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.