Canonical Allele Identifier: CA409105895

Gene: HNF4A

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_175914.5:c.439G>T MANE Select	NP_787110.2:p.Val147Phe
ENST00000316673.9:c.439G>T MANE Select	ENSP00000315180.4:p.Val147Phe
NM_000457.4:c.505G>T , LRG_483t2:c.505G>T	NP_000448.3:p.Val169Phe
NM_000457.5:c.505G>T	NP_000448.3:p.Val169Phe
NM_000457.6:c.505G>T	NP_000448.3:p.Val169Phe
NM_001030003.2:c.439G>T	NP_001025174.1:p.Val147Phe
NM_001030003.3:c.439G>T	NP_001025174.1:p.Val147Phe
NM_001030004.2:c.439G>T	NP_001025175.1:p.Val147Phe
NM_001030004.3:c.439G>T	NP_001025175.1:p.Val147Phe
NM_001258355.1:c.484G>T	NP_001245284.1:p.Val162Phe
NM_001258355.2:c.484G>T	NP_001245284.1:p.Val162Phe
NM_001287182.1:c.430G>T	NP_001274111.1:p.Val144Phe
NM_001287182.2:c.430G>T	NP_001274111.1:p.Val144Phe
NM_001287183.1:c.430G>T , LRG_483t3:c.430G>T	NP_001274112.1:p.Val144Phe
NM_001287183.2:c.430G>T	NP_001274112.1:p.Val144Phe
NM_001287184.1:c.430G>T	NP_001274113.1:p.Val144Phe
NM_001287184.2:c.430G>T	NP_001274113.1:p.Val144Phe
NM_175914.4:c.439G>T , LRG_483t1:c.439G>T	NP_787110.2:p.Val147Phe
NM_178849.2:c.505G>T	NP_849180.1:p.Val169Phe
NM_178849.3:c.505G>T	NP_849180.1:p.Val169Phe
NM_178850.2:c.505G>T	NP_849181.1:p.Val169Phe
NM_178850.3:c.505G>T	NP_849181.1:p.Val169Phe
ENST00000316099.10:c.505G>T	ENSP00000312987.3:p.Val169Phe
ENST00000316099.8:c.505G>T	ENSP00000312987.3:p.Val169Phe
ENST00000316099.9:c.505G>T	ENSP00000312987.3:p.Val169Phe
ENST00000316673.8:c.439G>T	ENSP00000315180.4:p.Val147Phe
ENST00000372920.1:c.*272G>T	ENSP00000362011.1:n.*272G>T
ENST00000415691.2:c.505G>T	ENSP00000412111.1:p.Val169Phe
ENST00000443598.6:c.505G>T	ENSP00000410911.2:p.Val169Phe
ENST00000457232.5:c.439G>T	ENSP00000396216.1:p.Val147Phe
ENST00000609795.5:c.439G>T	ENSP00000476609.1:p.Val147Phe
ENST00000619550.4:c.430G>T	ENSP00000481331.1:p.Val144Phe
ENST00000619550.5:c.479G>T
ENST00000683148.1:n.481G>T
ENST00000683657.1:n.1629G>T
XM_005260407.2:c.622G>T	XP_005260464.1:p.Val208Phe
XM_005260407.4:c.622G>T	XP_005260464.1:p.Val208Phe
XM_011528797.1:c.553G>T	XP_011527099.1:p.Val185Phe
XM_011528798.1:c.553G>T	XP_011527100.1:p.Val185Phe