Canonical Allele Identifier: CA409106086

Gene: HNF4A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44414610T>C , CM000682.2:g.44414610T>C	GRCh38
NC_000020.10:g.43043250T>C , CM000682.1:g.43043250T>C	GRCh37
NC_000020.9:g.42476664T>C	NCBI36
NG_009818.1:g.63810T>C , LRG_483:g.63810T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_175914.5:c.530T>C MANE Select	NP_787110.2:p.Val177Ala
ENST00000316673.9:c.530T>C MANE Select	ENSP00000315180.4:p.Val177Ala
NM_000457.4:c.596T>C , LRG_483t2:c.596T>C	NP_000448.3:p.Val199Ala
NM_000457.5:c.596T>C	NP_000448.3:p.Val199Ala
NM_000457.6:c.596T>C	NP_000448.3:p.Val199Ala
NM_001030003.2:c.530T>C	NP_001025174.1:p.Val177Ala
NM_001030003.3:c.530T>C	NP_001025174.1:p.Val177Ala
NM_001030004.2:c.530T>C	NP_001025175.1:p.Val177Ala
NM_001030004.3:c.530T>C	NP_001025175.1:p.Val177Ala
NM_001258355.1:c.575T>C	NP_001245284.1:p.Val192Ala
NM_001258355.2:c.575T>C	NP_001245284.1:p.Val192Ala
NM_001287182.1:c.521T>C	NP_001274111.1:p.Val174Ala
NM_001287182.2:c.521T>C	NP_001274111.1:p.Val174Ala
NM_001287183.1:c.521T>C , LRG_483t3:c.521T>C	NP_001274112.1:p.Val174Ala
NM_001287183.2:c.521T>C	NP_001274112.1:p.Val174Ala
NM_001287184.1:c.521T>C	NP_001274113.1:p.Val174Ala
NM_001287184.2:c.521T>C	NP_001274113.1:p.Val174Ala
NM_175914.4:c.530T>C , LRG_483t1:c.530T>C	NP_787110.2:p.Val177Ala
NM_178849.2:c.596T>C	NP_849180.1:p.Val199Ala
NM_178849.3:c.596T>C	NP_849180.1:p.Val199Ala
NM_178850.2:c.596T>C	NP_849181.1:p.Val199Ala
NM_178850.3:c.596T>C	NP_849181.1:p.Val199Ala
ENST00000316099.10:c.596T>C	ENSP00000312987.3:p.Val199Ala
ENST00000316099.8:c.596T>C	ENSP00000312987.3:p.Val199Ala
ENST00000316099.9:c.596T>C	ENSP00000312987.3:p.Val199Ala
ENST00000316673.8:c.530T>C	ENSP00000315180.4:p.Val177Ala
ENST00000372920.1:c.*363T>C	ENSP00000362011.1:n.*363T>C
ENST00000415691.2:c.596T>C	ENSP00000412111.1:p.Val199Ala
ENST00000443598.6:c.596T>C	ENSP00000410911.2:p.Val199Ala
ENST00000457232.5:c.530T>C	ENSP00000396216.1:p.Val177Ala
ENST00000609795.5:c.530T>C	ENSP00000476609.1:p.Val177Ala
ENST00000619550.4:c.521T>C	ENSP00000481331.1:p.Val174Ala
ENST00000619550.5:c.570T>C
ENST00000683148.1:n.572T>C
ENST00000683657.1:n.1720T>C
XM_005260407.2:c.713T>C	XP_005260464.1:p.Val238Ala
XM_005260407.4:c.713T>C	XP_005260464.1:p.Val238Ala
XM_011528797.1:c.644T>C	XP_011527099.1:p.Val215Ala
XM_011528798.1:c.644T>C	XP_011527100.1:p.Val215Ala