Human (GRCh38.p14)
Description

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

Location

Chromosome 15: 30,135,051-30,148,748 forward strand.

GRCh38:CM000677.2

View alleles of this gene on alternative sequences

About this gene

This gene has 2 transcripts (splice variants), 1 gene allele, 246 orthologues and 18 paralogues.

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