Canonical Allele Identifier: CA2365752969

Gene: HNF4A HNF4A-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44395422A= , CM000682.2:g.44395422A=	GRCh38
NC_000020.10:g.43024062A= , CM000682.1:g.43024062A=	GRCh37
NC_000020.9:g.42457476A=	NCBI36
NG_009818.1:g.44622A= , LRG_483:g.44622A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000316673.9:c.50-10636A= (HNF4A) MANE Select	ENSP00000315180.4:n.50-10636A=
ENST00000316673.8:c.50-10636A= (HNF4A)	ENSP00000315180.4:n.50-10636A=
ENST00000457232.5:c.50-10636A= (HNF4A)	ENSP00000396216.1:n.50-10636A=
ENST00000609262.5:c.40+4743A= (HNF4A)	ENSP00000476310.1:n.40+4743A=
ENST00000609795.5:c.50-10636A= (HNF4A)	ENSP00000476609.1:n.50-10636A=
ENST00000619550.4:c.40+4743A= (HNF4A)	ENSP00000481331.1:n.40+4743A=
NM_001030003.2:c.50-10636A= (HNF4A)	NP_001025174.1:n.50-10636A=
NM_001030004.2:c.50-10636A= (HNF4A)	NP_001025175.1:n.50-10636A=
NM_001287182.1:c.40+4743A= (HNF4A)	NP_001274111.1:n.40+4743A=
NM_001287183.1:c.40+4743A= , LRG_483t3:c.40+4743A= (HNF4A)	NP_001274112.1:n.40+4743A=
NM_001287184.1:c.40+4743A= (HNF4A)	NP_001274113.1:n.40+4743A=
NM_175914.4:c.50-10636A= , LRG_483t1:c.50-10636A= (HNF4A)	NP_787110.2:n.50-10636A=
NR_109949.1:n.254+31T= (HNF4A-AS1)
NM_001030003.3:c.50-10636A= (HNF4A)	NP_001025174.1:n.50-10636A=
NM_001030004.3:c.50-10636A= (HNF4A)	NP_001025175.1:n.50-10636A=
NM_001287182.2:c.40+4743A= (HNF4A)	NP_001274111.1:n.40+4743A=
NM_001287184.2:c.40+4743A= (HNF4A)	NP_001274113.1:n.40+4743A=
NM_001287183.2:c.40+4743A= (HNF4A)	NP_001274112.1:n.40+4743A=
NM_175914.5:c.50-10636A= (HNF4A) MANE Select	NP_787110.2:n.50-10636A=
NR_172878.1:n.210+31T= (HNF4A-AS1)
NR_172879.1:n.210+31T= (HNF4A-AS1)