Canonical Allele Identifier: CA2365764300

Gene: HNF4A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44419771_44419772delinsCG , CM000682.2:g.44419771_44419772delinsCG	GRCh38
NC_000020.10:g.43048411_43048412delinsCG , CM000682.1:g.43048411_43048412delinsCG	GRCh37
NC_000020.9:g.42481825_42481826delinsCG	NCBI36
NG_009818.1:g.68971_68972delinsCG , LRG_483:g.68971_68972delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316673.9:c.721_722delinsCG MANE Select	ENSP00000315180.4:p.Arg241=
ENST00000316099.10:c.787_788delinsCG	ENSP00000312987.3:p.Arg263=
ENST00000619550.5:c.761_762delinsCG
ENST00000683148.1:n.763_764delinsCG
ENST00000683657.1:n.1911_1912delinsCG
ENST00000316099.9:c.787_788delinsCG	ENSP00000312987.3:p.Arg263=
ENST00000316099.8:c.787_788delinsCG	ENSP00000312987.3:p.Arg263=
ENST00000316673.8:c.721_722delinsCG	ENSP00000315180.4:p.Arg241=
ENST00000372920.1:c.*554_*555delinsCG	ENSP00000362011.1:n.*554_*555delinsCG
ENST00000415691.2:c.787_788delinsCG	ENSP00000412111.1:p.Arg263=
ENST00000443598.6:c.787_788delinsCG	ENSP00000410911.2:p.Arg263=
ENST00000457232.5:c.721_722delinsCG	ENSP00000396216.1:p.Arg241=
ENST00000609795.5:c.721_722delinsCG	ENSP00000476609.1:p.Arg241=
ENST00000619550.4:c.712_713delinsCG	ENSP00000481331.1:p.Arg238=
NM_000457.4:c.787_788delinsCG , LRG_483t2:c.787_788delinsCG	NP_000448.3:p.Arg263=
NM_001030003.2:c.721_722delinsCG	NP_001025174.1:p.Arg241=
NM_001030004.2:c.721_722delinsCG	NP_001025175.1:p.Arg241=
NM_001258355.1:c.766_767delinsCG	NP_001245284.1:p.Arg256=
NM_001287182.1:c.712_713delinsCG	NP_001274111.1:p.Arg238=
NM_001287183.1:c.712_713delinsCG , LRG_483t3:c.712_713delinsCG	NP_001274112.1:p.Arg238=
NM_001287184.1:c.712_713delinsCG	NP_001274113.1:p.Arg238=
NM_175914.4:c.721_722delinsCG , LRG_483t1:c.721_722delinsCG	NP_787110.2:p.Arg241=
NM_178849.2:c.787_788delinsCG	NP_849180.1:p.Arg263=
NM_178850.2:c.787_788delinsCG	NP_849181.1:p.Arg263=
XM_005260407.2:c.904_905delinsCG	XP_005260464.1:p.Arg302=
XM_011528797.1:c.835_836delinsCG	XP_011527099.1:p.Arg279=
XM_011528798.1:c.835_836delinsCG	XP_011527100.1:p.Arg279=
XM_005260407.4:c.904_905delinsCG	XP_005260464.1:p.Arg302=
NM_001030003.3:c.721_722delinsCG	NP_001025174.1:p.Arg241=
NM_001030004.3:c.721_722delinsCG	NP_001025175.1:p.Arg241=
NM_001258355.2:c.766_767delinsCG	NP_001245284.1:p.Arg256=
NM_001287182.2:c.712_713delinsCG	NP_001274111.1:p.Arg238=
NM_001287184.2:c.712_713delinsCG	NP_001274113.1:p.Arg238=
NM_178849.3:c.787_788delinsCG	NP_849180.1:p.Arg263=
NM_178850.3:c.787_788delinsCG	NP_849181.1:p.Arg263=
NM_000457.5:c.787_788delinsCG	NP_000448.3:p.Arg263=
NM_000457.6:c.787_788delinsCG	NP_000448.3:p.Arg263=
NM_001287183.2:c.712_713delinsCG	NP_001274112.1:p.Arg238=
NM_175914.5:c.721_722delinsCG MANE Select	NP_787110.2:p.Arg241=