Human (GRCh38.p14)
Description

golgin A8 family member Q [Source:HGNC Symbol;Acc:HGNC:44408]

Location
About this transcript

This transcript has 19 exons, is annotated with 23 domains and features, is associated with 6234 variant alleles and maps to 3732 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000562783.2GOLGA8Q-2015110632aaENSP00000457904.1
 
Protein coding
CCDS86441H3BV12 NM_001355476.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000565941.1GOLGA8Q-202652No protein-
 
Protein coding CDS not defined
--TSL:5
Statistics

Exons: 19, Coding exons: 19, Transcript length: 5,110 bps, Translation length: 632 residues

MANE

This MANE Select transcript contains ENSP00000457904 and matches to NM_001355476.2 and NP_001342405.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: H3BV12

CCDS

This transcript is a member of the Human CCDS set: CCDS86441

Transcript Support Level (TSL)

TSL:5

Version

ENST00000562783.2

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.