Human (GRCh38.p14)
Description

golgin A8 family member T [Source:HGNC Symbol;Acc:HGNC:44410]

Location
About this transcript

This transcript has 19 exons, is annotated with 23 domains and features, is associated with 6167 variant alleles and maps to 3619 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000569052.2GOLGA8T-2025175631aaENSP00000455826.1
 
Protein coding
CCDS86440H3BQL2 NM_001355469.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000565649.1GOLGA8T-201573No protein-
 
Protein coding CDS not defined
--TSL:4
Statistics

Exons: 19, Coding exons: 19, Transcript length: 5,175 bps, Translation length: 631 residues

MANE

This MANE Select transcript contains ENSP00000455826 and matches to NM_001355469.2 and NP_001342398.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: H3BQL2

CCDS

This transcript is a member of the Human CCDS set: CCDS86440

Transcript Support Level (TSL)

TSL:5

Version

ENST00000569052.2

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

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