Canonical Allele Identifier: CA2816472252
Gene: HNF4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44413637_44413638insGG , CM000682.2:g.44413637_44413638insGG GRCh38
NC_000020.10:g.43042277_43042278insGG , CM000682.1:g.43042277_43042278insGG GRCh37
NC_000020.9:g.42475691_42475692insGG NCBI36
NG_009818.1:g.62837_62838insGG , LRG_483:g.62837_62838insGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000316673.9:c.320-57_320-56insGG MANE Select ENSP00000315180.4:n.320-57_320-56insGG
ENST00000316099.10:c.386-57_386-56insGG ENSP00000312987.3:n.386-57_386-56insGG
ENST00000619550.5:c.360-57_360-56insGG
ENST00000683148.1:n.362-57_362-56insGG
ENST00000683657.1:n.1510-57_1510-56insGG
ENST00000316099.9:c.386-57_386-56insGG ENSP00000312987.3:n.386-57_386-56insGG
ENST00000316099.8:c.386-57_386-56insGG ENSP00000312987.3:n.386-57_386-56insGG
ENST00000316673.8:c.320-57_320-56insGG ENSP00000315180.4:n.320-57_320-56insGG
ENST00000372920.1:c.*153-57_*153-56insGG ENSP00000362011.1:n.*153-57_*153-56insGG
ENST00000415691.2:c.386-57_386-56insGG ENSP00000412111.1:n.386-57_386-56insGG
ENST00000443598.6:c.386-57_386-56insGG ENSP00000410911.2:n.386-57_386-56insGG
ENST00000457232.5:c.320-57_320-56insGG ENSP00000396216.1:n.320-57_320-56insGG
ENST00000609795.5:c.320-57_320-56insGG ENSP00000476609.1:n.320-57_320-56insGG
ENST00000619550.4:c.311-57_311-56insGG ENSP00000481331.1:n.311-57_311-56insGG
NM_000457.4:c.386-57_386-56insGG , LRG_483t2:c.386-57_386-56insGG NP_000448.3:n.386-57_386-56insGG
NM_001030003.2:c.320-57_320-56insGG NP_001025174.1:n.320-57_320-56insGG
NM_001030004.2:c.320-57_320-56insGG NP_001025175.1:n.320-57_320-56insGG
NM_001258355.1:c.365-57_365-56insGG NP_001245284.1:n.365-57_365-56insGG
NM_001287182.1:c.311-57_311-56insGG NP_001274111.1:n.311-57_311-56insGG
NM_001287183.1:c.311-57_311-56insGG , LRG_483t3:c.311-57_311-56insGG NP_001274112.1:n.311-57_311-56insGG
NM_001287184.1:c.311-57_311-56insGG NP_001274113.1:n.311-57_311-56insGG
NM_175914.4:c.320-57_320-56insGG , LRG_483t1:c.320-57_320-56insGG NP_787110.2:n.320-57_320-56insGG
NM_178849.2:c.386-57_386-56insGG NP_849180.1:n.386-57_386-56insGG
NM_178850.2:c.386-57_386-56insGG NP_849181.1:n.386-57_386-56insGG
XM_005260407.2:c.503-57_503-56insGG XP_005260464.1:n.503-57_503-56insGG
XM_011528797.1:c.434-57_434-56insGG XP_011527099.1:n.434-57_434-56insGG
XM_011528798.1:c.434-57_434-56insGG XP_011527100.1:n.434-57_434-56insGG
XM_005260407.4:c.503-57_503-56insGG XP_005260464.1:n.503-57_503-56insGG
NM_001030003.3:c.320-57_320-56insGG NP_001025174.1:n.320-57_320-56insGG
NM_001030004.3:c.320-57_320-56insGG NP_001025175.1:n.320-57_320-56insGG
NM_001258355.2:c.365-57_365-56insGG NP_001245284.1:n.365-57_365-56insGG
NM_001287182.2:c.311-57_311-56insGG NP_001274111.1:n.311-57_311-56insGG
NM_001287184.2:c.311-57_311-56insGG NP_001274113.1:n.311-57_311-56insGG
NM_178849.3:c.386-57_386-56insGG NP_849180.1:n.386-57_386-56insGG
NM_178850.3:c.386-57_386-56insGG NP_849181.1:n.386-57_386-56insGG
NM_000457.5:c.386-57_386-56insGG NP_000448.3:n.386-57_386-56insGG
NM_000457.6:c.386-57_386-56insGG NP_000448.3:n.386-57_386-56insGG
NM_001287183.2:c.311-57_311-56insGG NP_001274112.1:n.311-57_311-56insGG
NM_175914.5:c.320-57_320-56insGG MANE Select NP_787110.2:n.320-57_320-56insGG