Canonical Allele Identifier: CA2365761547
Gene: HNF4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44413709G= , CM000682.2:g.44413709G= GRCh38
NC_000020.10:g.43042349G= , CM000682.1:g.43042349G= GRCh37
NC_000020.9:g.42475763G= NCBI36
NG_009818.1:g.62909G= , LRG_483:g.62909G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000316673.9:c.335G= MANE Select ENSP00000315180.4:p.Arg112=
ENST00000316099.10:c.401G= ENSP00000312987.3:p.Arg134=
ENST00000619550.5:c.375G=
ENST00000683148.1:n.377G=
ENST00000683657.1:n.1525G=
ENST00000316099.9:c.401G= ENSP00000312987.3:p.Arg134=
ENST00000316099.8:c.401G= ENSP00000312987.3:p.Arg134=
ENST00000316673.8:c.335G= ENSP00000315180.4:p.Arg112=
ENST00000372920.1:c.*168G= ENSP00000362011.1:n.*168G=
ENST00000415691.2:c.401G= ENSP00000412111.1:p.Arg134=
ENST00000443598.6:c.401G= ENSP00000410911.2:p.Arg134=
ENST00000457232.5:c.335G= ENSP00000396216.1:p.Arg112=
ENST00000609795.5:c.335G= ENSP00000476609.1:p.Arg112=
ENST00000619550.4:c.326G= ENSP00000481331.1:p.Arg109=
NM_000457.4:c.401G= , LRG_483t2:c.401G= NP_000448.3:p.Arg134=
NM_001030003.2:c.335G= NP_001025174.1:p.Arg112=
NM_001030004.2:c.335G= NP_001025175.1:p.Arg112=
NM_001258355.1:c.380G= NP_001245284.1:p.Arg127=
NM_001287182.1:c.326G= NP_001274111.1:p.Arg109=
NM_001287183.1:c.326G= , LRG_483t3:c.326G= NP_001274112.1:p.Arg109=
NM_001287184.1:c.326G= NP_001274113.1:p.Arg109=
NM_175914.4:c.335G= , LRG_483t1:c.335G= NP_787110.2:p.Arg112=
NM_178849.2:c.401G= NP_849180.1:p.Arg134=
NM_178850.2:c.401G= NP_849181.1:p.Arg134=
XM_005260407.2:c.518G= XP_005260464.1:p.Arg173=
XM_011528797.1:c.449G= XP_011527099.1:p.Arg150=
XM_011528798.1:c.449G= XP_011527100.1:p.Arg150=
XM_005260407.4:c.518G= XP_005260464.1:p.Arg173=
NM_001030003.3:c.335G= NP_001025174.1:p.Arg112=
NM_001030004.3:c.335G= NP_001025175.1:p.Arg112=
NM_001258355.2:c.380G= NP_001245284.1:p.Arg127=
NM_001287182.2:c.326G= NP_001274111.1:p.Arg109=
NM_001287184.2:c.326G= NP_001274113.1:p.Arg109=
NM_178849.3:c.401G= NP_849180.1:p.Arg134=
NM_178850.3:c.401G= NP_849181.1:p.Arg134=
NM_000457.5:c.401G= NP_000448.3:p.Arg134=
NM_000457.6:c.401G= NP_000448.3:p.Arg134=
NM_001287183.2:c.326G= NP_001274112.1:p.Arg109=
NM_175914.5:c.335G= MANE Select NP_787110.2:p.Arg112=