Canonical Allele Identifier: CA2365761572
Gene: HNF4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44413773C= , CM000682.2:g.44413773C= GRCh38
NC_000020.10:g.43042413C= , CM000682.1:g.43042413C= GRCh37
NC_000020.9:g.42475827C= NCBI36
NG_009818.1:g.62973C= , LRG_483:g.62973C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000316673.9:c.399C= MANE Select ENSP00000315180.4:p.Leu133=
ENST00000316099.10:c.465C= ENSP00000312987.3:p.Leu155=
ENST00000619550.5:c.439C=
ENST00000683148.1:n.441C=
ENST00000683657.1:n.1589C=
ENST00000316099.9:c.465C= ENSP00000312987.3:p.Leu155=
ENST00000316099.8:c.465C= ENSP00000312987.3:p.Leu155=
ENST00000316673.8:c.399C= ENSP00000315180.4:p.Leu133=
ENST00000372920.1:c.*232C= ENSP00000362011.1:n.*232C=
ENST00000415691.2:c.465C= ENSP00000412111.1:p.Leu155=
ENST00000443598.6:c.465C= ENSP00000410911.2:p.Leu155=
ENST00000457232.5:c.399C= ENSP00000396216.1:p.Leu133=
ENST00000609795.5:c.399C= ENSP00000476609.1:p.Leu133=
ENST00000619550.4:c.390C= ENSP00000481331.1:p.Leu130=
NM_000457.4:c.465C= , LRG_483t2:c.465C= NP_000448.3:p.Leu155=
NM_001030003.2:c.399C= NP_001025174.1:p.Leu133=
NM_001030004.2:c.399C= NP_001025175.1:p.Leu133=
NM_001258355.1:c.444C= NP_001245284.1:p.Leu148=
NM_001287182.1:c.390C= NP_001274111.1:p.Leu130=
NM_001287183.1:c.390C= , LRG_483t3:c.390C= NP_001274112.1:p.Leu130=
NM_001287184.1:c.390C= NP_001274113.1:p.Leu130=
NM_175914.4:c.399C= , LRG_483t1:c.399C= NP_787110.2:p.Leu133=
NM_178849.2:c.465C= NP_849180.1:p.Leu155=
NM_178850.2:c.465C= NP_849181.1:p.Leu155=
XM_005260407.2:c.582C= XP_005260464.1:p.Leu194=
XM_011528797.1:c.513C= XP_011527099.1:p.Leu171=
XM_011528798.1:c.513C= XP_011527100.1:p.Leu171=
XM_005260407.4:c.582C= XP_005260464.1:p.Leu194=
NM_001030003.3:c.399C= NP_001025174.1:p.Leu133=
NM_001030004.3:c.399C= NP_001025175.1:p.Leu133=
NM_001258355.2:c.444C= NP_001245284.1:p.Leu148=
NM_001287182.2:c.390C= NP_001274111.1:p.Leu130=
NM_001287184.2:c.390C= NP_001274113.1:p.Leu130=
NM_178849.3:c.465C= NP_849180.1:p.Leu155=
NM_178850.3:c.465C= NP_849181.1:p.Leu155=
NM_000457.5:c.465C= NP_000448.3:p.Leu155=
NM_000457.6:c.465C= NP_000448.3:p.Leu155=
NM_001287183.2:c.390C= NP_001274112.1:p.Leu130=
NM_175914.5:c.399C= MANE Select NP_787110.2:p.Leu133=