Canonical Allele Identifier: CA510582824

Gene: HNF4A

Linked Data

• MyVariant Identifiers: chr20:g.43048383G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44419743G>C , CM000682.2:g.44419743G>C	GRCh38
NC_000020.10:g.43048383G>C , CM000682.1:g.43048383G>C	GRCh37
NC_000020.9:g.42481797G>C	NCBI36
NG_009818.1:g.68943G>C , LRG_483:g.68943G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316673.9:c.693G>C MANE Select	ENSP00000315180.4:p.Arg231=
ENST00000316099.10:c.759G>C	ENSP00000312987.3:p.Arg253=
ENST00000619550.5:c.733G>C
ENST00000683148.1:n.735G>C
ENST00000683657.1:n.1883G>C
ENST00000316099.9:c.759G>C	ENSP00000312987.3:p.Arg253=
ENST00000316099.8:c.759G>C	ENSP00000312987.3:p.Arg253=
ENST00000316673.8:c.693G>C	ENSP00000315180.4:p.Arg231=
ENST00000372920.1:c.*526G>C	ENSP00000362011.1:n.*526G>C
ENST00000415691.2:c.759G>C	ENSP00000412111.1:p.Arg253=
ENST00000443598.6:c.759G>C	ENSP00000410911.2:p.Arg253=
ENST00000457232.5:c.693G>C	ENSP00000396216.1:p.Arg231=
ENST00000609795.5:c.693G>C	ENSP00000476609.1:p.Arg231=
ENST00000619550.4:c.684G>C	ENSP00000481331.1:p.Arg228=
NM_000457.4:c.759G>C , LRG_483t2:c.759G>C	NP_000448.3:p.Arg253=
NM_001030003.2:c.693G>C	NP_001025174.1:p.Arg231=
NM_001030004.2:c.693G>C	NP_001025175.1:p.Arg231=
NM_001258355.1:c.738G>C	NP_001245284.1:p.Arg246=
NM_001287182.1:c.684G>C	NP_001274111.1:p.Arg228=
NM_001287183.1:c.684G>C , LRG_483t3:c.684G>C	NP_001274112.1:p.Arg228=
NM_001287184.1:c.684G>C	NP_001274113.1:p.Arg228=
NM_175914.4:c.693G>C , LRG_483t1:c.693G>C	NP_787110.2:p.Arg231=
NM_178849.2:c.759G>C	NP_849180.1:p.Arg253=
NM_178850.2:c.759G>C	NP_849181.1:p.Arg253=
XM_005260407.2:c.876G>C	XP_005260464.1:p.Arg292=
XM_011528797.1:c.807G>C	XP_011527099.1:p.Arg269=
XM_011528798.1:c.807G>C	XP_011527100.1:p.Arg269=
XM_005260407.4:c.876G>C	XP_005260464.1:p.Arg292=
NM_001030003.3:c.693G>C	NP_001025174.1:p.Arg231=
NM_001030004.3:c.693G>C	NP_001025175.1:p.Arg231=
NM_001258355.2:c.738G>C	NP_001245284.1:p.Arg246=
NM_001287182.2:c.684G>C	NP_001274111.1:p.Arg228=
NM_001287184.2:c.684G>C	NP_001274113.1:p.Arg228=
NM_178849.3:c.759G>C	NP_849180.1:p.Arg253=
NM_178850.3:c.759G>C	NP_849181.1:p.Arg253=
NM_000457.5:c.759G>C	NP_000448.3:p.Arg253=
NM_000457.6:c.759G>C	NP_000448.3:p.Arg253=
NM_001287183.2:c.684G>C	NP_001274112.1:p.Arg228=
NM_175914.5:c.693G>C MANE Select	NP_787110.2:p.Arg231=