Human (GRCh38.p14)
Description

chromosome 12 open reading frame 40 [Source:HGNC Symbol;Acc:HGNC:26846]

Gene Synonyms

FLJ40126

Location
About this transcript

This transcript has 13 exons, is annotated with 10 domains and features, is associated with 50568 variant alleles and maps to 380 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000324616.9C12orf40-2012776652aaENSP00000317671.5
 
Protein coding
CCDS41770Q86WS4-1 NM_001031748.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000405531.7C12orf40-2021656477aaENSP00000383897.3
 
Protein coding
CCDS81681Q86WS4-2 -GENCODE basicTSL:1
ENST00000468200.2C12orf40-2033061394aaENSP00000473371.1
 
Nonsense mediated decay
Q86WS4-3 -TSL:1
Statistics

Exons: 13, Coding exons: 13, Transcript length: 2,776 bps, Translation length: 652 residues

MANE

This MANE Select transcript contains ENSP00000317671 and matches to NM_001031748.4 and NP_001026918.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q86WS4

CCDS

This transcript is a member of the Human CCDS set: CCDS41770

Transcript Support Level (TSL)

TSL:1

Version

ENST00000324616.9

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.