Human (GRCh38.p14)
Description

golgin A8 family member R [Source:HGNC Symbol;Acc:HGNC:44407]

Location
About this transcript

This transcript has 19 exons, is annotated with 21 domains and features, is associated with 4235 variant alleles and maps to 3608 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000327271.11GOLGA8R-2015172631aaENSP00000323217.10
 
Protein coding
CCDS61575I6L899-1 NM_001282484.1MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000624918.1GOLGA8R-2023062No protein-
 
TEC
--TSL:NA
Statistics

Exons: 19, Coding exons: 19, Transcript length: 5,172 bps, Translation length: 631 residues

MANE

This MANE Select transcript contains ENSP00000323217 and matches to NM_001282484.1 and NP_001269413.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: I6L899

CCDS

This transcript is a member of the Human CCDS set: CCDS61575

Transcript Support Level (TSL)

TSL:5

Version

ENST00000327271.11

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.

Annotation Attributes

dotter confirmed [Definitions]

GENCODE basic gene

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