Canonical Allele Identifier: CA409105774
Gene: HNF4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44413784A>C , CM000682.2:g.44413784A>C GRCh38
NC_000020.10:g.43042424A>C , CM000682.1:g.43042424A>C GRCh37
NC_000020.9:g.42475838A>C NCBI36
NG_009818.1:g.62984A>C , LRG_483:g.62984A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000316673.9:c.410A>C MANE Select ENSP00000315180.4:p.Glu137Ala
ENST00000316099.10:c.476A>C ENSP00000312987.3:p.Glu159Ala
ENST00000619550.5:c.450A>C
ENST00000683148.1:n.452A>C
ENST00000683657.1:n.1600A>C
ENST00000316099.9:c.476A>C ENSP00000312987.3:p.Glu159Ala
ENST00000316099.8:c.476A>C ENSP00000312987.3:p.Glu159Ala
ENST00000316673.8:c.410A>C ENSP00000315180.4:p.Glu137Ala
ENST00000372920.1:c.*243A>C ENSP00000362011.1:n.*243A>C
ENST00000415691.2:c.476A>C ENSP00000412111.1:p.Glu159Ala
ENST00000443598.6:c.476A>C ENSP00000410911.2:p.Glu159Ala
ENST00000457232.5:c.410A>C ENSP00000396216.1:p.Glu137Ala
ENST00000609795.5:c.410A>C ENSP00000476609.1:p.Glu137Ala
ENST00000619550.4:c.401A>C ENSP00000481331.1:p.Glu134Ala
NM_000457.4:c.476A>C , LRG_483t2:c.476A>C NP_000448.3:p.Glu159Ala
NM_001030003.2:c.410A>C NP_001025174.1:p.Glu137Ala
NM_001030004.2:c.410A>C NP_001025175.1:p.Glu137Ala
NM_001258355.1:c.455A>C NP_001245284.1:p.Glu152Ala
NM_001287182.1:c.401A>C NP_001274111.1:p.Glu134Ala
NM_001287183.1:c.401A>C , LRG_483t3:c.401A>C NP_001274112.1:p.Glu134Ala
NM_001287184.1:c.401A>C NP_001274113.1:p.Glu134Ala
NM_175914.4:c.410A>C , LRG_483t1:c.410A>C NP_787110.2:p.Glu137Ala
NM_178849.2:c.476A>C NP_849180.1:p.Glu159Ala
NM_178850.2:c.476A>C NP_849181.1:p.Glu159Ala
XM_005260407.2:c.593A>C XP_005260464.1:p.Glu198Ala
XM_011528797.1:c.524A>C XP_011527099.1:p.Glu175Ala
XM_011528798.1:c.524A>C XP_011527100.1:p.Glu175Ala
XM_005260407.4:c.593A>C XP_005260464.1:p.Glu198Ala
NM_001030003.3:c.410A>C NP_001025174.1:p.Glu137Ala
NM_001030004.3:c.410A>C NP_001025175.1:p.Glu137Ala
NM_001258355.2:c.455A>C NP_001245284.1:p.Glu152Ala
NM_001287182.2:c.401A>C NP_001274111.1:p.Glu134Ala
NM_001287184.2:c.401A>C NP_001274113.1:p.Glu134Ala
NM_178849.3:c.476A>C NP_849180.1:p.Glu159Ala
NM_178850.3:c.476A>C NP_849181.1:p.Glu159Ala
NM_000457.5:c.476A>C NP_000448.3:p.Glu159Ala
NM_000457.6:c.476A>C NP_000448.3:p.Glu159Ala
NM_001287183.2:c.401A>C NP_001274112.1:p.Glu134Ala
NM_175914.5:c.410A>C MANE Select NP_787110.2:p.Glu137Ala