Canonical Allele Identifier: CA2365768294

Gene: HNF4A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44428840G= , CM000682.2:g.44428840G=	GRCh38
NC_000020.10:g.43057480G= , CM000682.1:g.43057480G=	GRCh37
NC_000020.9:g.42490894G=	NCBI36
NG_009818.1:g.78040G= , LRG_483:g.78040G=

Transcript Alleles

HGVS	Amino-acid Change
NM_175914.5:c.1216+353G= MANE Select	NP_787110.2:n.1216+353G=
ENST00000316673.9:c.1216+353G= MANE Select	ENSP00000315180.4:n.1216+353G=
NM_000457.4:c.1282+353G= , LRG_483t2:c.1282+353G=	NP_000448.3:n.1282+353G=
NM_000457.5:c.1282+353G=	NP_000448.3:n.1282+353G=
NM_000457.6:c.1282+353G=	NP_000448.3:n.1282+353G=
NM_001030003.2:c.1186+383G=	NP_001025174.1:n.1186+383G=
NM_001030003.3:c.1186+383G=	NP_001025174.1:n.1186+383G=
NM_001258355.1:c.1261+353G=	NP_001245284.1:n.1261+353G=
NM_001258355.2:c.1261+353G=	NP_001245284.1:n.1261+353G=
NM_001287182.1:c.1177+383G=	NP_001274111.1:n.1177+383G=
NM_001287182.2:c.1177+383G=	NP_001274111.1:n.1177+383G=
NM_001287183.1:c.1207+353G= , LRG_483t3:c.1207+353G=	NP_001274112.1:n.1207+353G=
NM_001287183.2:c.1207+353G=	NP_001274112.1:n.1207+353G=
NM_175914.4:c.1216+353G= , LRG_483t1:c.1216+353G=	NP_787110.2:n.1216+353G=
NM_178849.2:c.1252+383G=	NP_849180.1:n.1252+383G=
NM_178849.3:c.1252+383G=	NP_849180.1:n.1252+383G=
ENST00000316099.10:c.1282+353G=	ENSP00000312987.3:n.1282+353G=
ENST00000316099.8:c.1282+353G=	ENSP00000312987.3:n.1282+353G=
ENST00000316099.9:c.1282+353G=	ENSP00000312987.3:n.1282+353G=
ENST00000316673.8:c.1216+353G=	ENSP00000315180.4:n.1216+353G=
ENST00000372920.1:c.*1049+353G=	ENSP00000362011.1:n.*1049+353G=
ENST00000415691.2:c.1252+383G=	ENSP00000412111.1:n.1252+383G=
ENST00000457232.5:c.1186+383G=	ENSP00000396216.1:n.1186+383G=
ENST00000619550.4:c.1207+353G=	ENSP00000481331.1:n.1207+353G=
XM_005260407.2:c.1399+353G=	XP_005260464.1:n.1399+353G=
XM_005260407.4:c.1399+353G=	XP_005260464.1:n.1399+353G=
XM_011528797.1:c.1300+383G=	XP_011527099.1:n.1300+383G=
XM_011528798.1:c.1330+353G=	XP_011527100.1:n.1330+353G=