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Human (GRCh38.p14)
Description

HNF1 homeobox B [Source:HGNC Symbol;Acc:HGNC:11630]

Gene Synonyms

HNF1B, HNF1BETA, LFB3, MODY5, TCF2, VHNF1

Location

Chromosome 17: 37,686,431-37,745,059 reverse strand.

GRCh38:CM000679.2

View alleles of this gene on alternative sequences

About this gene

This gene has 5 transcripts (splice variants), 1 gene allele, 218 orthologues, 1 paralogue and is associated with 13 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000617811.5HNF1B-2032790557aaENSP00000480291.1
 
Protein coding
CCDS11324P35680-1 NM_000458.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicTSL:1
ENST00000621123.4HNF1B-2051971531aaENSP00000482711.1
 
Protein coding
CCDS58538P35680-2 -GENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000614313.4HNF1B-2021819548aaENSP00000482529.1
 
Protein coding
CCDS92293A0A087WZC2 -GENCODE PrimaryGENCODE BasicTSL:5
ENST00000613727.4HNF1B-2011546457aaENSP00000477524.1
 
Protein coding
CCDS77007A0A0C4DGS8 -GENCODE PrimaryGENCODE BasicTSL:1
ENST00000618894.1HNF1B-2043481No protein-
 
Retained intron
--TSL:2