Human (GRCh38.p14)
Description

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

Gene Synonyms

HNF1B, HNF1BETA, LFB3, MODY5, TCF2, VHNF1

Location
About this transcript

This transcript has 2 exons, is associated with 2399 variant alleles and maps to 199 oligo probes.

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

Exons: 2, Coding exons: 0, Transcript length: 3,481 bps,

Transcript Support Level (TSL)

TSL:2

Version

ENST00000618894.1

Type

Retained intron

Annotation Method

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