Human (GRCh38.p14)
Description

negative regulator of P-body association [Source:HGNC Symbol;Acc:HGNC:50713]

Gene Synonyms

LINC01420, NOBODY

Location
About this transcript

This transcript has 3 exons, is annotated with 3 domains and features, is associated with 25623 variant alleles and maps to 429 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000374922.9NBDY-201234468aaENSP00000489583.1
 
Protein coding
CCDS87751A0A0U1RRE5 A0A4P8PLQ7 NM_001348129.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000637096.1NBDY-20489668aaENSP00000490217.1
 
Protein coding
CCDS87751A0A0U1RRE5 A0A4P8PLQ7 -GENCODE basicAPPRIS P1TSL:3
ENST00000423617.2NBDY-20254368aaENSP00000489486.1
 
Protein coding
CCDS87751A0A0U1RRE5 A0A4P8PLQ7 -GENCODE basicAPPRIS P1TSL:2
ENST00000451583.1NBDY-20330540aaENSP00000489367.1
 
Nonsense mediated decay
A0A0U1RR68 -TSL:5CDS 5' incomplete
Statistics

Exons: 3, Coding exons: 1, Transcript length: 2,344 bps, Translation length: 68 residues

MANE

This MANE Select transcript contains ENSP00000489583 and matches to NM_001348129.2 and NP_001335058.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: A0A0U1RRE5

CCDS

This transcript is a member of the Human CCDS set: CCDS87751

Transcript Support Level (TSL)

TSL:1

Version

ENST00000374922.9

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

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