Canonical Allele Identifier: CA2365761943

Gene: HNF4A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44414519G= , CM000682.2:g.44414519G=	GRCh38
NC_000020.10:g.43043159G= , CM000682.1:g.43043159G=	GRCh37
NC_000020.9:g.42476573G=	NCBI36
NG_009818.1:g.63719G= , LRG_483:g.63719G=

Transcript Alleles

HGVS	Amino-acid Change
NM_175914.5:c.439G= MANE Select	NP_787110.2:p.Val147=
ENST00000316673.9:c.439G= MANE Select	ENSP00000315180.4:p.Val147=
NM_000457.4:c.505G= , LRG_483t2:c.505G=	NP_000448.3:p.Val169=
NM_000457.5:c.505G=	NP_000448.3:p.Val169=
NM_000457.6:c.505G=	NP_000448.3:p.Val169=
NM_001030003.2:c.439G=	NP_001025174.1:p.Val147=
NM_001030003.3:c.439G=	NP_001025174.1:p.Val147=
NM_001030004.2:c.439G=	NP_001025175.1:p.Val147=
NM_001030004.3:c.439G=	NP_001025175.1:p.Val147=
NM_001258355.1:c.484G=	NP_001245284.1:p.Val162=
NM_001258355.2:c.484G=	NP_001245284.1:p.Val162=
NM_001287182.1:c.430G=	NP_001274111.1:p.Val144=
NM_001287182.2:c.430G=	NP_001274111.1:p.Val144=
NM_001287183.1:c.430G= , LRG_483t3:c.430G=	NP_001274112.1:p.Val144=
NM_001287183.2:c.430G=	NP_001274112.1:p.Val144=
NM_001287184.1:c.430G=	NP_001274113.1:p.Val144=
NM_001287184.2:c.430G=	NP_001274113.1:p.Val144=
NM_175914.4:c.439G= , LRG_483t1:c.439G=	NP_787110.2:p.Val147=
NM_178849.2:c.505G=	NP_849180.1:p.Val169=
NM_178849.3:c.505G=	NP_849180.1:p.Val169=
NM_178850.2:c.505G=	NP_849181.1:p.Val169=
NM_178850.3:c.505G=	NP_849181.1:p.Val169=
ENST00000316099.10:c.505G=	ENSP00000312987.3:p.Val169=
ENST00000316099.8:c.505G=	ENSP00000312987.3:p.Val169=
ENST00000316099.9:c.505G=	ENSP00000312987.3:p.Val169=
ENST00000316673.8:c.439G=	ENSP00000315180.4:p.Val147=
ENST00000372920.1:c.*272G=	ENSP00000362011.1:n.*272G=
ENST00000415691.2:c.505G=	ENSP00000412111.1:p.Val169=
ENST00000443598.6:c.505G=	ENSP00000410911.2:p.Val169=
ENST00000457232.5:c.439G=	ENSP00000396216.1:p.Val147=
ENST00000609795.5:c.439G=	ENSP00000476609.1:p.Val147=
ENST00000619550.4:c.430G=	ENSP00000481331.1:p.Val144=
ENST00000619550.5:c.479G=
ENST00000683148.1:n.481G=
ENST00000683657.1:n.1629G=
XM_005260407.2:c.622G=	XP_005260464.1:p.Val208=
XM_005260407.4:c.622G=	XP_005260464.1:p.Val208=
XM_011528797.1:c.553G=	XP_011527099.1:p.Val185=
XM_011528798.1:c.553G=	XP_011527100.1:p.Val185=