Canonical Allele Identifier: CA2652974086

Gene: HNF4A

Linked Data

• gnomAD v4: 20-44429851-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44429851C>A , CM000682.2:g.44429851C>A	GRCh38
NC_000020.10:g.43058491C>A , CM000682.1:g.43058491C>A	GRCh37
NC_000020.9:g.42491905C>A	NCBI36
NG_009818.1:g.79051C>A , LRG_483:g.79051C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000316673.9:c.*186C>A MANE Select	ENSP00000315180.4:n.*186C>A
ENST00000316099.10:c.*186C>A	ENSP00000312987.3:n.*186C>A
ENST00000316099.9:c.*186C>A	ENSP00000312987.3:n.*186C>A
ENST00000316099.8:c.*186C>A	ENSP00000312987.3:n.*186C>A
ENST00000372920.1:c.*1378C>A	ENSP00000362011.1:n.*1378C>A
ENST00000415691.2:c.*186C>A	ENSP00000412111.1:n.*186C>A
ENST00000619550.4:c.*186C>A	ENSP00000481331.1:n.*186C>A
NM_000457.4:c.*186C>A , LRG_483t2:c.*186C>A	NP_000448.3:n.*186C>A
NM_001030003.2:c.*186C>A	NP_001025174.1:n.*186C>A
NM_001258355.1:c.*186C>A	NP_001245284.1:n.*186C>A
NM_001287182.1:c.*186C>A	NP_001274111.1:n.*186C>A
NM_001287183.1:c.*186C>A , LRG_483t3:c.*186C>A	NP_001274112.1:n.*186C>A
NM_175914.4:c.*186C>A , LRG_483t1:c.*186C>A	NP_787110.2:n.*186C>A
NM_178849.2:c.*186C>A	NP_849180.1:n.*186C>A
XM_005260407.2:c.*186C>A	XP_005260464.1:n.*186C>A
XM_011528797.1:c.*186C>A	XP_011527099.1:n.*186C>A
XM_011528798.1:c.*186C>A	XP_011527100.1:n.*186C>A
XM_005260407.4:c.*186C>A	XP_005260464.1:n.*186C>A
NM_001030003.3:c.*186C>A	NP_001025174.1:n.*186C>A
NM_001258355.2:c.*186C>A	NP_001245284.1:n.*186C>A
NM_001287182.2:c.*186C>A	NP_001274111.1:n.*186C>A
NM_178849.3:c.*186C>A	NP_849180.1:n.*186C>A
NM_000457.5:c.*186C>A	NP_000448.3:n.*186C>A
NM_000457.6:c.*186C>A	NP_000448.3:n.*186C>A
NM_001287183.2:c.*186C>A	NP_001274112.1:n.*186C>A
NM_175914.5:c.*186C>A MANE Select	NP_787110.2:n.*186C>A