Canonical Allele Identifier: CA2652970752

Gene: HNF4A HNF4A-AS1

Linked Data

• gnomAD v4: 20-44395386-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44395386G>T , CM000682.2:g.44395386G>T	GRCh38
NC_000020.10:g.43024026G>T , CM000682.1:g.43024026G>T	GRCh37
NC_000020.9:g.42457440G>T	NCBI36
NG_009818.1:g.44586G>T , LRG_483:g.44586G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316673.9:c.50-10672G>T (HNF4A) MANE Select	ENSP00000315180.4:n.50-10672G>T
ENST00000316673.8:c.50-10672G>T (HNF4A)	ENSP00000315180.4:n.50-10672G>T
ENST00000457232.5:c.50-10672G>T (HNF4A)	ENSP00000396216.1:n.50-10672G>T
ENST00000609262.5:c.40+4707G>T (HNF4A)	ENSP00000476310.1:n.40+4707G>T
ENST00000609795.5:c.50-10672G>T (HNF4A)	ENSP00000476609.1:n.50-10672G>T
ENST00000619550.4:c.40+4707G>T (HNF4A)	ENSP00000481331.1:n.40+4707G>T
NM_001030003.2:c.50-10672G>T (HNF4A)	NP_001025174.1:n.50-10672G>T
NM_001030004.2:c.50-10672G>T (HNF4A)	NP_001025175.1:n.50-10672G>T
NM_001287182.1:c.40+4707G>T (HNF4A)	NP_001274111.1:n.40+4707G>T
NM_001287183.1:c.40+4707G>T , LRG_483t3:c.40+4707G>T (HNF4A)	NP_001274112.1:n.40+4707G>T
NM_001287184.1:c.40+4707G>T (HNF4A)	NP_001274113.1:n.40+4707G>T
NM_175914.4:c.50-10672G>T , LRG_483t1:c.50-10672G>T (HNF4A)	NP_787110.2:n.50-10672G>T
NR_109949.1:n.254+67C>A (HNF4A-AS1)
NM_001030003.3:c.50-10672G>T (HNF4A)	NP_001025174.1:n.50-10672G>T
NM_001030004.3:c.50-10672G>T (HNF4A)	NP_001025175.1:n.50-10672G>T
NM_001287182.2:c.40+4707G>T (HNF4A)	NP_001274111.1:n.40+4707G>T
NM_001287184.2:c.40+4707G>T (HNF4A)	NP_001274113.1:n.40+4707G>T
NM_001287183.2:c.40+4707G>T (HNF4A)	NP_001274112.1:n.40+4707G>T
NM_175914.5:c.50-10672G>T (HNF4A) MANE Select	NP_787110.2:n.50-10672G>T
NR_172878.1:n.210+67C>A (HNF4A-AS1)
NR_172879.1:n.210+67C>A (HNF4A-AS1)