Human (GRCh38.p14)
Description

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

Location
About this transcript

This transcript has 2 exons, is associated with 8449 variant alleles and maps to 42 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: 2, Coding exons: 0, Transcript length: 695 bps,

Transcript Support Level (TSL)

TSL:3

Version

ENST00000569811.1

Type

Protein coding CDS not defined

Annotation Method

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