Canonical Allele Identifier: CA2652973985

Gene: HNF4A

Linked Data

• gnomAD v4: 20-44429751-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44429751G>C , CM000682.2:g.44429751G>C	GRCh38
NC_000020.10:g.43058391G>C , CM000682.1:g.43058391G>C	GRCh37
NC_000020.9:g.42491805G>C	NCBI36
NG_009818.1:g.78951G>C , LRG_483:g.78951G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000316673.9:c.*86G>C MANE Select	ENSP00000315180.4:n.*86G>C
ENST00000316099.10:c.*86G>C	ENSP00000312987.3:n.*86G>C
ENST00000316099.9:c.*86G>C	ENSP00000312987.3:n.*86G>C
ENST00000316099.8:c.*86G>C	ENSP00000312987.3:n.*86G>C
ENST00000372920.1:c.*1278G>C	ENSP00000362011.1:n.*1278G>C
ENST00000415691.2:c.*86G>C	ENSP00000412111.1:n.*86G>C
ENST00000619550.4:c.*86G>C	ENSP00000481331.1:n.*86G>C
NM_000457.4:c.*86G>C , LRG_483t2:c.*86G>C	NP_000448.3:n.*86G>C
NM_001030003.2:c.*86G>C	NP_001025174.1:n.*86G>C
NM_001258355.1:c.*86G>C	NP_001245284.1:n.*86G>C
NM_001287182.1:c.*86G>C	NP_001274111.1:n.*86G>C
NM_001287183.1:c.*86G>C , LRG_483t3:c.*86G>C	NP_001274112.1:n.*86G>C
NM_175914.4:c.*86G>C , LRG_483t1:c.*86G>C	NP_787110.2:n.*86G>C
NM_178849.2:c.*86G>C	NP_849180.1:n.*86G>C
XM_005260407.2:c.*86G>C	XP_005260464.1:n.*86G>C
XM_011528797.1:c.*86G>C	XP_011527099.1:n.*86G>C
XM_011528798.1:c.*86G>C	XP_011527100.1:n.*86G>C
XM_005260407.4:c.*86G>C	XP_005260464.1:n.*86G>C
NM_001030003.3:c.*86G>C	NP_001025174.1:n.*86G>C
NM_001258355.2:c.*86G>C	NP_001245284.1:n.*86G>C
NM_001287182.2:c.*86G>C	NP_001274111.1:n.*86G>C
NM_178849.3:c.*86G>C	NP_849180.1:n.*86G>C
NM_000457.5:c.*86G>C	NP_000448.3:n.*86G>C
NM_000457.6:c.*86G>C	NP_000448.3:n.*86G>C
NM_001287183.2:c.*86G>C	NP_001274112.1:n.*86G>C
NM_175914.5:c.*86G>C MANE Select	NP_787110.2:n.*86G>C