Human (GRCh38.p14)
Description

forkhead box A1 [Source:HGNC Symbol;Acc:HGNC:5021]

Gene Synonyms

HNF3A

Location
About this transcript

This transcript has 2 exons, is annotated with 27 domains and features, is associated with 5031 variant alleles and maps to 284 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000250448.5FOXA1-2013509472aaENSP00000250448.3
 
Protein coding
CCDS9665P55317-1 NM_004496.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000553751.1FOXA1-20350736aaENSP00000451704.1
 
Nonsense mediated decay
G3V4B9 -TSL:4
ENST00000545425.2FOXA1-2021806No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000554607.1FOXA1-204789No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000557418.1FOXA1-205392No protein-
 
Protein coding CDS not defined
--TSL:3
Statistics

Exons: 2, Coding exons: 2, Transcript length: 3,509 bps, Translation length: 472 residues

MANE

This MANE Select transcript contains ENSP00000250448 and matches to NM_004496.5 and NP_004487.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: P55317

CCDS

This transcript is a member of the Human CCDS set: CCDS9665

Transcript Support Level (TSL)

TSL:1

Version

ENST00000250448.5

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.