Human (GRCh38.p14)
Description

forkhead box A3 [Source:HGNC Symbol;Acc:HGNC:5023]

Gene Synonyms

HNF3G

Location
About this transcript

This transcript has 2 exons, is annotated with 21 domains and features, is associated with 4674 variant alleles and maps to 256 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000302177.3FOXA3-2011923350aaENSP00000304004.1
 
Protein coding
CCDS12677A0A024R0R3 P55318 NM_004497.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000594297.1FOXA3-202538101aaENSP00000470816.1
 
Protein coding
M0QZW5 -TSL:3CDS 3' incomplete
Statistics

Exons: 2, Coding exons: 2, Transcript length: 1,923 bps, Translation length: 350 residues

MANE

This MANE Select transcript contains ENSP00000304004 and matches to NM_004497.3 and NP_004488.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: P55318

CCDS

This transcript is a member of the Human CCDS set: CCDS12677

Transcript Support Level (TSL)

TSL:1

Version

ENST00000302177.3

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.