Human (GRCh38.p14)
Description

golgin A8 family member B [Source:HGNC Symbol;Acc:HGNC:31973]

Location
About this transcript

This transcript has 24 exons, is annotated with 22 domains and features, is associated with 20980 variant alleles and maps to 2580 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000683415.1GOLGA8B-2115607603aaENSP00000507830.1
 
Protein coding
CCDS45211A8MQT2-1 NM_001023567.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2
ENST00000342314.9GOLGA8B-2014335603aaENSP00000343064.5
 
Protein coding
CCDS45211A8MQT2-1 -GENCODE basicAPPRIS P2TSL:1
ENST00000438958.2GOLGA8B-2024252633aaENSP00000400063.2
 
Protein coding
C9J1B5 -GENCODE basicAPPRIS ALT2TSL:5
ENST00000569811.1GOLGA8B-210695No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000564575.5GOLGA8B-205574No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000566258.1GOLGA8B-207540No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000566091.5GOLGA8B-206529No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000562282.5GOLGA8B-204463No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000569100.5GOLGA8B-2096488No protein-
 
Retained intron
--TSL:5
ENST00000484716.5GOLGA8B-2036114No protein-
 
Retained intron
--TSL:1
ENST00000568555.1GOLGA8B-2082328No protein-
 
Retained intron
--TSL:1
Statistics

Exons: 24, Coding exons: 16, Transcript length: 5,607 bps, Translation length: 603 residues

MANE

This MANE Select transcript contains ENSP00000507830 and matches to NM_001023567.5 and NP_001018861.3

Uniprot

This transcript corresponds to the following Uniprot identifiers: A8MQT2

CCDS

This transcript is a member of the Human CCDS set: CCDS45211

Version

ENST00000683415.1

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.