Human (GRCh38.p14)
Description

HIG1 hypoxia inducible domain family member 1B [Source:HGNC Symbol;Acc:HGNC:24318]

Gene Synonyms

CLST11240, CLST11240-15

Location
About this transcript

This transcript has 3 exons, is annotated with 8 domains and features, is associated with 1405 variant alleles and maps to 206 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000253410.3HIGD1B-20165099aaENSP00000253410.1
 
Protein coding
CCDS11488Q9P298 NM_016438.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000591513.5HIGD1B-20554799aaENSP00000468511.1
 
Protein coding
CCDS11488Q9P298 -GENCODE basicAPPRIS P1TSL:2
ENST00000587021.1HIGD1B-20345754aaENSP00000464703.1
 
Protein coding
K7EID5 -GENCODE basicTSL:2
ENST00000586911.1HIGD1B-20247040aaENSP00000465657.1
 
Nonsense mediated decay
K7EKK1 -TSL:3CDS 5' incomplete
ENST00000590423.1HIGD1B-204321No protein-
 
Protein coding CDS not defined
--TSL:5
Statistics

Exons: 3, Coding exons: 3, Transcript length: 650 bps, Translation length: 99 residues

MANE

This MANE Select transcript contains ENSP00000253410 and matches to NM_016438.4 and NP_057522.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9P298

CCDS

This transcript is a member of the Human CCDS set: CCDS11488

Transcript Support Level (TSL)

TSL:1

Version

ENST00000253410.3

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.