Canonical Allele Identifier: CA409110114

Gene: HNF4A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44428409G>T , CM000682.2:g.44428409G>T	GRCh38
NC_000020.10:g.43057049G>T , CM000682.1:g.43057049G>T	GRCh37
NC_000020.9:g.42490463G>T	NCBI36
NG_009818.1:g.77609G>T , LRG_483:g.77609G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_175914.5:c.1138G>T MANE Select	NP_787110.2:p.Val380Phe
ENST00000316673.9:c.1138G>T MANE Select	ENSP00000315180.4:p.Val380Phe
NM_000457.4:c.1204G>T , LRG_483t2:c.1204G>T	NP_000448.3:p.Val402Phe
NM_000457.5:c.1204G>T	NP_000448.3:p.Val402Phe
NM_000457.6:c.1204G>T	NP_000448.3:p.Val402Phe
NM_001030003.2:c.1138G>T	NP_001025174.1:p.Val380Phe
NM_001030003.3:c.1138G>T	NP_001025174.1:p.Val380Phe
NM_001258355.1:c.1183G>T	NP_001245284.1:p.Val395Phe
NM_001258355.2:c.1183G>T	NP_001245284.1:p.Val395Phe
NM_001287182.1:c.1129G>T	NP_001274111.1:p.Val377Phe
NM_001287182.2:c.1129G>T	NP_001274111.1:p.Val377Phe
NM_001287183.1:c.1129G>T , LRG_483t3:c.1129G>T	NP_001274112.1:p.Val377Phe
NM_001287183.2:c.1129G>T	NP_001274112.1:p.Val377Phe
NM_175914.4:c.1138G>T , LRG_483t1:c.1138G>T	NP_787110.2:p.Val380Phe
NM_178849.2:c.1204G>T	NP_849180.1:p.Val402Phe
NM_178849.3:c.1204G>T	NP_849180.1:p.Val402Phe
ENST00000316099.10:c.1204G>T	ENSP00000312987.3:p.Val402Phe
ENST00000316099.8:c.1204G>T	ENSP00000312987.3:p.Val402Phe
ENST00000316099.9:c.1204G>T	ENSP00000312987.3:p.Val402Phe
ENST00000316673.8:c.1138G>T	ENSP00000315180.4:p.Val380Phe
ENST00000372920.1:c.*971G>T	ENSP00000362011.1:n.*971G>T
ENST00000415691.2:c.1204G>T	ENSP00000412111.1:p.Val402Phe
ENST00000457232.5:c.1138G>T	ENSP00000396216.1:p.Val380Phe
ENST00000619550.4:c.1129G>T	ENSP00000481331.1:p.Val377Phe
XM_005260407.2:c.1321G>T	XP_005260464.1:p.Val441Phe
XM_005260407.4:c.1321G>T	XP_005260464.1:p.Val441Phe
XM_011528797.1:c.1252G>T	XP_011527099.1:p.Val418Phe
XM_011528798.1:c.1252G>T	XP_011527100.1:p.Val418Phe