Human (GRCh38.p14)
Description

golgin A8 family member H [Source:HGNC Symbol;Acc:HGNC:37443]

Gene Synonyms

GOLGA6L11

Location
About this transcript

This transcript has 19 exons, is annotated with 24 domains and features, is associated with 8827 variant alleles and maps to 3456 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000566740.2GOLGA8H-2015188632aaENSP00000456894.1
 
Protein coding
CCDS61576P0CJ92 NM_001282490.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
Statistics

Exons: 19, Coding exons: 19, Transcript length: 5,188 bps, Translation length: 632 residues

MANE

This MANE Select transcript contains ENSP00000456894 and matches to NM_001282490.2 and NP_001269419.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: P0CJ92

CCDS

This transcript is a member of the Human CCDS set: CCDS61576

Transcript Support Level (TSL)

TSL:5

Version

ENST00000566740.2

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.