Human (GRCh38.p14)
Description

golgin A8 family member M [Source:HGNC Symbol;Acc:HGNC:44404]

Location
About this transcript

This transcript has 19 exons, is annotated with 23 domains and features, is associated with 7721 variant alleles and maps to 3680 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000563027.2GOLGA8M-2015368632aaENSP00000456927.1
 
Protein coding
CCDS61572H3BSY2-1 NM_001282468.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000563213.1GOLGA8M-202564No protein-
 
Protein coding CDS not defined
--TSL:5
Statistics

Exons: 19, Coding exons: 19, Transcript length: 5,368 bps, Translation length: 632 residues

MANE

This MANE Select transcript contains ENSP00000456927 and matches to NM_001282468.3 and NP_001269397.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: H3BSY2

CCDS

This transcript is a member of the Human CCDS set: CCDS61572

Transcript Support Level (TSL)

TSL:5

Version

ENST00000563027.2

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.