Canonical Allele Identifier: CA2365761656
Gene: HNF4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44413930_44413932delinsGAC , CM000682.2:g.44413930_44413932delinsGAC GRCh38
NC_000020.10:g.43042570_43042572delinsGAC , CM000682.1:g.43042570_43042572delinsGAC GRCh37
NC_000020.9:g.42475984_42475986delinsGAC NCBI36
NG_009818.1:g.63130_63132delinsGAC , LRG_483:g.63130_63132delinsGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000316673.9:c.426+130_426+132delinsGAC MANE Select ENSP00000315180.4:n.426+130_426+132delinsGAC
ENST00000316099.10:c.492+130_492+132delinsGAC ENSP00000312987.3:n.492+130_492+132delinsGAC
ENST00000619550.5:c.466+130_466+132delinsGAC
ENST00000683148.1:n.468+130_468+132delinsGAC
ENST00000683657.1:n.1616+130_1616+132delinsGAC
ENST00000316099.9:c.492+130_492+132delinsGAC ENSP00000312987.3:n.492+130_492+132delinsGAC
ENST00000316099.8:c.492+130_492+132delinsGAC ENSP00000312987.3:n.492+130_492+132delinsGAC
ENST00000316673.8:c.426+130_426+132delinsGAC ENSP00000315180.4:n.426+130_426+132delinsGAC
ENST00000372920.1:c.*259+130_*259+132delinsGAC ENSP00000362011.1:n.*259+130_*259+132delinsGAC
ENST00000415691.2:c.492+130_492+132delinsGAC ENSP00000412111.1:n.492+130_492+132delinsGAC
ENST00000443598.6:c.492+130_492+132delinsGAC ENSP00000410911.2:n.492+130_492+132delinsGAC
ENST00000457232.5:c.426+130_426+132delinsGAC ENSP00000396216.1:n.426+130_426+132delinsGAC
ENST00000609795.5:c.426+130_426+132delinsGAC ENSP00000476609.1:n.426+130_426+132delinsGAC
ENST00000619550.4:c.417+130_417+132delinsGAC ENSP00000481331.1:n.417+130_417+132delinsGAC
NM_000457.4:c.492+130_492+132delinsGAC , LRG_483t2:c.492+130_492+132delinsGAC NP_000448.3:n.492+130_492+132delinsGAC
NM_001030003.2:c.426+130_426+132delinsGAC NP_001025174.1:n.426+130_426+132delinsGAC
NM_001030004.2:c.426+130_426+132delinsGAC NP_001025175.1:n.426+130_426+132delinsGAC
NM_001258355.1:c.471+130_471+132delinsGAC NP_001245284.1:n.471+130_471+132delinsGAC
NM_001287182.1:c.417+130_417+132delinsGAC NP_001274111.1:n.417+130_417+132delinsGAC
NM_001287183.1:c.417+130_417+132delinsGAC , LRG_483t3:c.417+130_417+132delinsGAC NP_001274112.1:n.417+130_417+132delinsGAC
NM_001287184.1:c.417+130_417+132delinsGAC NP_001274113.1:n.417+130_417+132delinsGAC
NM_175914.4:c.426+130_426+132delinsGAC , LRG_483t1:c.426+130_426+132delinsGAC NP_787110.2:n.426+130_426+132delinsGAC
NM_178849.2:c.492+130_492+132delinsGAC NP_849180.1:n.492+130_492+132delinsGAC
NM_178850.2:c.492+130_492+132delinsGAC NP_849181.1:n.492+130_492+132delinsGAC
XM_005260407.2:c.609+130_609+132delinsGAC XP_005260464.1:n.609+130_609+132delinsGAC
XM_011528797.1:c.540+130_540+132delinsGAC XP_011527099.1:n.540+130_540+132delinsGAC
XM_011528798.1:c.540+130_540+132delinsGAC XP_011527100.1:n.540+130_540+132delinsGAC
XM_005260407.4:c.609+130_609+132delinsGAC XP_005260464.1:n.609+130_609+132delinsGAC
NM_001030003.3:c.426+130_426+132delinsGAC NP_001025174.1:n.426+130_426+132delinsGAC
NM_001030004.3:c.426+130_426+132delinsGAC NP_001025175.1:n.426+130_426+132delinsGAC
NM_001258355.2:c.471+130_471+132delinsGAC NP_001245284.1:n.471+130_471+132delinsGAC
NM_001287182.2:c.417+130_417+132delinsGAC NP_001274111.1:n.417+130_417+132delinsGAC
NM_001287184.2:c.417+130_417+132delinsGAC NP_001274113.1:n.417+130_417+132delinsGAC
NM_178849.3:c.492+130_492+132delinsGAC NP_849180.1:n.492+130_492+132delinsGAC
NM_178850.3:c.492+130_492+132delinsGAC NP_849181.1:n.492+130_492+132delinsGAC
NM_000457.5:c.492+130_492+132delinsGAC NP_000448.3:n.492+130_492+132delinsGAC
NM_000457.6:c.492+130_492+132delinsGAC NP_000448.3:n.492+130_492+132delinsGAC
NM_001287183.2:c.417+130_417+132delinsGAC NP_001274112.1:n.417+130_417+132delinsGAC
NM_175914.5:c.426+130_426+132delinsGAC MANE Select NP_787110.2:n.426+130_426+132delinsGAC