Canonical Allele Identifier: CA2365752965

Gene: HNF4A HNF4A-AS1

Linked Data

• dbSNP Id: rs2425637

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44395409G>A , CM000682.2:g.44395409G>A	GRCh38
NC_000020.10:g.43024049G>A , CM000682.1:g.43024049G>A	GRCh37
NC_000020.9:g.42457463G>A	NCBI36
NG_009818.1:g.44609G>A , LRG_483:g.44609G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000316673.9:c.50-10649G>A (HNF4A) MANE Select	ENSP00000315180.4:n.50-10649G>A
ENST00000316673.8:c.50-10649G>A (HNF4A)	ENSP00000315180.4:n.50-10649G>A
ENST00000457232.5:c.50-10649G>A (HNF4A)	ENSP00000396216.1:n.50-10649G>A
ENST00000609262.5:c.40+4730G>A (HNF4A)	ENSP00000476310.1:n.40+4730G>A
ENST00000609795.5:c.50-10649G>A (HNF4A)	ENSP00000476609.1:n.50-10649G>A
ENST00000619550.4:c.40+4730G>A (HNF4A)	ENSP00000481331.1:n.40+4730G>A
NM_001030003.2:c.50-10649G>A (HNF4A)	NP_001025174.1:n.50-10649G>A
NM_001030004.2:c.50-10649G>A (HNF4A)	NP_001025175.1:n.50-10649G>A
NM_001287182.1:c.40+4730G>A (HNF4A)	NP_001274111.1:n.40+4730G>A
NM_001287183.1:c.40+4730G>A , LRG_483t3:c.40+4730G>A (HNF4A)	NP_001274112.1:n.40+4730G>A
NM_001287184.1:c.40+4730G>A (HNF4A)	NP_001274113.1:n.40+4730G>A
NM_175914.4:c.50-10649G>A , LRG_483t1:c.50-10649G>A (HNF4A)	NP_787110.2:n.50-10649G>A
NR_109949.1:n.254+44C>T (HNF4A-AS1)
NM_001030003.3:c.50-10649G>A (HNF4A)	NP_001025174.1:n.50-10649G>A
NM_001030004.3:c.50-10649G>A (HNF4A)	NP_001025175.1:n.50-10649G>A
NM_001287182.2:c.40+4730G>A (HNF4A)	NP_001274111.1:n.40+4730G>A
NM_001287184.2:c.40+4730G>A (HNF4A)	NP_001274113.1:n.40+4730G>A
NM_001287183.2:c.40+4730G>A (HNF4A)	NP_001274112.1:n.40+4730G>A
NM_175914.5:c.50-10649G>A (HNF4A) MANE Select	NP_787110.2:n.50-10649G>A
NR_172878.1:n.210+44C>T (HNF4A-AS1)
NR_172879.1:n.210+44C>T (HNF4A-AS1)