Canonical Allele Identifier: CA2652974090

Gene: HNF4A

Linked Data

• gnomAD v4: 20-44429859-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44429859A>G , CM000682.2:g.44429859A>G	GRCh38
NC_000020.10:g.43058499A>G , CM000682.1:g.43058499A>G	GRCh37
NC_000020.9:g.42491913A>G	NCBI36
NG_009818.1:g.79059A>G , LRG_483:g.79059A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000316673.9:c.*194A>G MANE Select	ENSP00000315180.4:n.*194A>G
ENST00000316099.10:c.*194A>G	ENSP00000312987.3:n.*194A>G
ENST00000316099.9:c.*194A>G	ENSP00000312987.3:n.*194A>G
ENST00000316099.8:c.*194A>G	ENSP00000312987.3:n.*194A>G
ENST00000372920.1:c.*1386A>G	ENSP00000362011.1:n.*1386A>G
ENST00000415691.2:c.*194A>G	ENSP00000412111.1:n.*194A>G
ENST00000619550.4:c.*194A>G	ENSP00000481331.1:n.*194A>G
NM_000457.4:c.*194A>G , LRG_483t2:c.*194A>G	NP_000448.3:n.*194A>G
NM_001030003.2:c.*194A>G	NP_001025174.1:n.*194A>G
NM_001258355.1:c.*194A>G	NP_001245284.1:n.*194A>G
NM_001287182.1:c.*194A>G	NP_001274111.1:n.*194A>G
NM_001287183.1:c.*194A>G , LRG_483t3:c.*194A>G	NP_001274112.1:n.*194A>G
NM_175914.4:c.*194A>G , LRG_483t1:c.*194A>G	NP_787110.2:n.*194A>G
NM_178849.2:c.*194A>G	NP_849180.1:n.*194A>G
XM_005260407.2:c.*194A>G	XP_005260464.1:n.*194A>G
XM_011528797.1:c.*194A>G	XP_011527099.1:n.*194A>G
XM_011528798.1:c.*194A>G	XP_011527100.1:n.*194A>G
XM_005260407.4:c.*194A>G	XP_005260464.1:n.*194A>G
NM_001030003.3:c.*194A>G	NP_001025174.1:n.*194A>G
NM_001258355.2:c.*194A>G	NP_001245284.1:n.*194A>G
NM_001287182.2:c.*194A>G	NP_001274111.1:n.*194A>G
NM_178849.3:c.*194A>G	NP_849180.1:n.*194A>G
NM_000457.5:c.*194A>G	NP_000448.3:n.*194A>G
NM_000457.6:c.*194A>G	NP_000448.3:n.*194A>G
NM_001287183.2:c.*194A>G	NP_001274112.1:n.*194A>G
NM_175914.5:c.*194A>G MANE Select	NP_787110.2:n.*194A>G