Canonical Allele Identifier: CA2365761528
Gene: HNF4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44413664_44413667delinsCCCT , CM000682.2:g.44413664_44413667delinsCCCT GRCh38
NC_000020.10:g.43042304_43042307delinsCCCT , CM000682.1:g.43042304_43042307delinsCCCT GRCh37
NC_000020.9:g.42475718_42475721delinsCCCT NCBI36
NG_009818.1:g.62864_62867delinsCCCT , LRG_483:g.62864_62867delinsCCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000316673.9:c.320-30_320-27delinsCCCT MANE Select ENSP00000315180.4:n.320-30_320-27delinsCCCT
ENST00000316099.10:c.386-30_386-27delinsCCCT ENSP00000312987.3:n.386-30_386-27delinsCCCT
ENST00000619550.5:c.360-30_360-27delinsCCCT
ENST00000683148.1:n.362-30_362-27delinsCCCT
ENST00000683657.1:n.1510-30_1510-27delinsCCCT
ENST00000316099.9:c.386-30_386-27delinsCCCT ENSP00000312987.3:n.386-30_386-27delinsCCCT
ENST00000316099.8:c.386-30_386-27delinsCCCT ENSP00000312987.3:n.386-30_386-27delinsCCCT
ENST00000316673.8:c.320-30_320-27delinsCCCT ENSP00000315180.4:n.320-30_320-27delinsCCCT
ENST00000372920.1:c.*153-30_*153-27delinsCCCT ENSP00000362011.1:n.*153-30_*153-27delinsCCCT
ENST00000415691.2:c.386-30_386-27delinsCCCT ENSP00000412111.1:n.386-30_386-27delinsCCCT
ENST00000443598.6:c.386-30_386-27delinsCCCT ENSP00000410911.2:n.386-30_386-27delinsCCCT
ENST00000457232.5:c.320-30_320-27delinsCCCT ENSP00000396216.1:n.320-30_320-27delinsCCCT
ENST00000609795.5:c.320-30_320-27delinsCCCT ENSP00000476609.1:n.320-30_320-27delinsCCCT
ENST00000619550.4:c.311-30_311-27delinsCCCT ENSP00000481331.1:n.311-30_311-27delinsCCCT
NM_000457.4:c.386-30_386-27delinsCCCT , LRG_483t2:c.386-30_386-27delinsCCCT NP_000448.3:n.386-30_386-27delinsCCCT
NM_001030003.2:c.320-30_320-27delinsCCCT NP_001025174.1:n.320-30_320-27delinsCCCT
NM_001030004.2:c.320-30_320-27delinsCCCT NP_001025175.1:n.320-30_320-27delinsCCCT
NM_001258355.1:c.365-30_365-27delinsCCCT NP_001245284.1:n.365-30_365-27delinsCCCT
NM_001287182.1:c.311-30_311-27delinsCCCT NP_001274111.1:n.311-30_311-27delinsCCCT
NM_001287183.1:c.311-30_311-27delinsCCCT , LRG_483t3:c.311-30_311-27delinsCCCT NP_001274112.1:n.311-30_311-27delinsCCCT
NM_001287184.1:c.311-30_311-27delinsCCCT NP_001274113.1:n.311-30_311-27delinsCCCT
NM_175914.4:c.320-30_320-27delinsCCCT , LRG_483t1:c.320-30_320-27delinsCCCT NP_787110.2:n.320-30_320-27delinsCCCT
NM_178849.2:c.386-30_386-27delinsCCCT NP_849180.1:n.386-30_386-27delinsCCCT
NM_178850.2:c.386-30_386-27delinsCCCT NP_849181.1:n.386-30_386-27delinsCCCT
XM_005260407.2:c.503-30_503-27delinsCCCT XP_005260464.1:n.503-30_503-27delinsCCCT
XM_011528797.1:c.434-30_434-27delinsCCCT XP_011527099.1:n.434-30_434-27delinsCCCT
XM_011528798.1:c.434-30_434-27delinsCCCT XP_011527100.1:n.434-30_434-27delinsCCCT
XM_005260407.4:c.503-30_503-27delinsCCCT XP_005260464.1:n.503-30_503-27delinsCCCT
NM_001030003.3:c.320-30_320-27delinsCCCT NP_001025174.1:n.320-30_320-27delinsCCCT
NM_001030004.3:c.320-30_320-27delinsCCCT NP_001025175.1:n.320-30_320-27delinsCCCT
NM_001258355.2:c.365-30_365-27delinsCCCT NP_001245284.1:n.365-30_365-27delinsCCCT
NM_001287182.2:c.311-30_311-27delinsCCCT NP_001274111.1:n.311-30_311-27delinsCCCT
NM_001287184.2:c.311-30_311-27delinsCCCT NP_001274113.1:n.311-30_311-27delinsCCCT
NM_178849.3:c.386-30_386-27delinsCCCT NP_849180.1:n.386-30_386-27delinsCCCT
NM_178850.3:c.386-30_386-27delinsCCCT NP_849181.1:n.386-30_386-27delinsCCCT
NM_000457.5:c.386-30_386-27delinsCCCT NP_000448.3:n.386-30_386-27delinsCCCT
NM_000457.6:c.386-30_386-27delinsCCCT NP_000448.3:n.386-30_386-27delinsCCCT
NM_001287183.2:c.311-30_311-27delinsCCCT NP_001274112.1:n.311-30_311-27delinsCCCT
NM_175914.5:c.320-30_320-27delinsCCCT MANE Select NP_787110.2:n.320-30_320-27delinsCCCT