Canonical Allele Identifier: CA2365761582
Gene: HNF4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44413790_44413791delinsTG , CM000682.2:g.44413790_44413791delinsTG GRCh38
NC_000020.10:g.43042430_43042431delinsTG , CM000682.1:g.43042430_43042431delinsTG GRCh37
NC_000020.9:g.42475844_42475845delinsTG NCBI36
NG_009818.1:g.62990_62991delinsTG , LRG_483:g.62990_62991delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000316673.9:c.416_417delinsTG MANE Select ENSP00000315180.4:p.Leu139=
ENST00000316099.10:c.482_483delinsTG ENSP00000312987.3:p.Leu161=
ENST00000619550.5:c.456_457delinsTG
ENST00000683148.1:n.458_459delinsTG
ENST00000683657.1:n.1606_1607delinsTG
ENST00000316099.9:c.482_483delinsTG ENSP00000312987.3:p.Leu161=
ENST00000316099.8:c.482_483delinsTG ENSP00000312987.3:p.Leu161=
ENST00000316673.8:c.416_417delinsTG ENSP00000315180.4:p.Leu139=
ENST00000372920.1:c.*249_*250delinsTG ENSP00000362011.1:n.*249_*250delinsTG
ENST00000415691.2:c.482_483delinsTG ENSP00000412111.1:p.Leu161=
ENST00000443598.6:c.482_483delinsTG ENSP00000410911.2:p.Leu161=
ENST00000457232.5:c.416_417delinsTG ENSP00000396216.1:p.Leu139=
ENST00000609795.5:c.416_417delinsTG ENSP00000476609.1:p.Leu139=
ENST00000619550.4:c.407_408delinsTG ENSP00000481331.1:p.Leu136=
NM_000457.4:c.482_483delinsTG , LRG_483t2:c.482_483delinsTG NP_000448.3:p.Leu161=
NM_001030003.2:c.416_417delinsTG NP_001025174.1:p.Leu139=
NM_001030004.2:c.416_417delinsTG NP_001025175.1:p.Leu139=
NM_001258355.1:c.461_462delinsTG NP_001245284.1:p.Leu154=
NM_001287182.1:c.407_408delinsTG NP_001274111.1:p.Leu136=
NM_001287183.1:c.407_408delinsTG , LRG_483t3:c.407_408delinsTG NP_001274112.1:p.Leu136=
NM_001287184.1:c.407_408delinsTG NP_001274113.1:p.Leu136=
NM_175914.4:c.416_417delinsTG , LRG_483t1:c.416_417delinsTG NP_787110.2:p.Leu139=
NM_178849.2:c.482_483delinsTG NP_849180.1:p.Leu161=
NM_178850.2:c.482_483delinsTG NP_849181.1:p.Leu161=
XM_005260407.2:c.599_600delinsTG XP_005260464.1:p.Leu200=
XM_011528797.1:c.530_531delinsTG XP_011527099.1:p.Leu177=
XM_011528798.1:c.530_531delinsTG XP_011527100.1:p.Leu177=
XM_005260407.4:c.599_600delinsTG XP_005260464.1:p.Leu200=
NM_001030003.3:c.416_417delinsTG NP_001025174.1:p.Leu139=
NM_001030004.3:c.416_417delinsTG NP_001025175.1:p.Leu139=
NM_001258355.2:c.461_462delinsTG NP_001245284.1:p.Leu154=
NM_001287182.2:c.407_408delinsTG NP_001274111.1:p.Leu136=
NM_001287184.2:c.407_408delinsTG NP_001274113.1:p.Leu136=
NM_178849.3:c.482_483delinsTG NP_849180.1:p.Leu161=
NM_178850.3:c.482_483delinsTG NP_849181.1:p.Leu161=
NM_000457.5:c.482_483delinsTG NP_000448.3:p.Leu161=
NM_000457.6:c.482_483delinsTG NP_000448.3:p.Leu161=
NM_001287183.2:c.407_408delinsTG NP_001274112.1:p.Leu136=
NM_175914.5:c.416_417delinsTG MANE Select NP_787110.2:p.Leu139=