Human (GRCh38.p14)
Description

galectin 9B [Source:HGNC Symbol;Acc:HGNC:24842]

Location
About this transcript

This transcript has 11 exons, is annotated with 19 domains and features, is associated with 7240 variant alleles and maps to 769 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000423676.8LGALS9B-2021718356aaENSP00000388841.3
 
Protein coding
CCDS92280Q3B8N2-1 NM_001367292.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P4TSL:1
ENST00000324290.5LGALS9B-2011243355aaENSP00000315564.5
 
Protein coding
CCDS42283Q3B8N2-2 -GENCODE basicAPPRIS ALT1TSL:5
ENST00000578481.5LGALS9B-203111535aaENSP00000464627.1
 
Nonsense mediated decay
J3QSC5 -TSL:2
ENST00000584703.1LGALS9B-20637551aaENSP00000464309.1
 
Nonsense mediated decay
J3QRN8 -TSL:3CDS 5' incomplete
ENST00000581490.1LGALS9B-205564No protein-
 
Retained intron
--TSL:5
ENST00000578724.1LGALS9B-204492No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 11, Coding exons: 11, Transcript length: 1,718 bps, Translation length: 356 residues

MANE

This MANE Select transcript contains ENSP00000388841 and matches to NM_001367292.2 and NP_001354221.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q3B8N2

CCDS

This transcript is a member of the Human CCDS set: CCDS92280

Transcript Support Level (TSL)

TSL:1

Version

ENST00000423676.8

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.