Canonical Allele Identifier: CA409107359

Gene: HNF4A

Linked Data

• MyVariant Identifiers: chr20:g.43048382G>C (hg19) ; chr20:g.44419742G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44419742G>C , CM000682.2:g.44419742G>C	GRCh38
NC_000020.10:g.43048382G>C , CM000682.1:g.43048382G>C	GRCh37
NC_000020.9:g.42481796G>C	NCBI36
NG_009818.1:g.68942G>C , LRG_483:g.68942G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316673.9:c.692G>C MANE Select	ENSP00000315180.4:p.Arg231Pro
ENST00000316099.10:c.758G>C	ENSP00000312987.3:p.Arg253Pro
ENST00000619550.5:c.732G>C
ENST00000683148.1:n.734G>C
ENST00000683657.1:n.1882G>C
ENST00000316099.9:c.758G>C	ENSP00000312987.3:p.Arg253Pro
ENST00000316099.8:c.758G>C	ENSP00000312987.3:p.Arg253Pro
ENST00000316673.8:c.692G>C	ENSP00000315180.4:p.Arg231Pro
ENST00000372920.1:c.*525G>C	ENSP00000362011.1:n.*525G>C
ENST00000415691.2:c.758G>C	ENSP00000412111.1:p.Arg253Pro
ENST00000443598.6:c.758G>C	ENSP00000410911.2:p.Arg253Pro
ENST00000457232.5:c.692G>C	ENSP00000396216.1:p.Arg231Pro
ENST00000609795.5:c.692G>C	ENSP00000476609.1:p.Arg231Pro
ENST00000619550.4:c.683G>C	ENSP00000481331.1:p.Arg228Pro
NM_000457.4:c.758G>C , LRG_483t2:c.758G>C	NP_000448.3:p.Arg253Pro
NM_001030003.2:c.692G>C	NP_001025174.1:p.Arg231Pro
NM_001030004.2:c.692G>C	NP_001025175.1:p.Arg231Pro
NM_001258355.1:c.737G>C	NP_001245284.1:p.Arg246Pro
NM_001287182.1:c.683G>C	NP_001274111.1:p.Arg228Pro
NM_001287183.1:c.683G>C , LRG_483t3:c.683G>C	NP_001274112.1:p.Arg228Pro
NM_001287184.1:c.683G>C	NP_001274113.1:p.Arg228Pro
NM_175914.4:c.692G>C , LRG_483t1:c.692G>C	NP_787110.2:p.Arg231Pro
NM_178849.2:c.758G>C	NP_849180.1:p.Arg253Pro
NM_178850.2:c.758G>C	NP_849181.1:p.Arg253Pro
XM_005260407.2:c.875G>C	XP_005260464.1:p.Arg292Pro
XM_011528797.1:c.806G>C	XP_011527099.1:p.Arg269Pro
XM_011528798.1:c.806G>C	XP_011527100.1:p.Arg269Pro
XM_005260407.4:c.875G>C	XP_005260464.1:p.Arg292Pro
NM_001030003.3:c.692G>C	NP_001025174.1:p.Arg231Pro
NM_001030004.3:c.692G>C	NP_001025175.1:p.Arg231Pro
NM_001258355.2:c.737G>C	NP_001245284.1:p.Arg246Pro
NM_001287182.2:c.683G>C	NP_001274111.1:p.Arg228Pro
NM_001287184.2:c.683G>C	NP_001274113.1:p.Arg228Pro
NM_178849.3:c.758G>C	NP_849180.1:p.Arg253Pro
NM_178850.3:c.758G>C	NP_849181.1:p.Arg253Pro
NM_000457.5:c.758G>C	NP_000448.3:p.Arg253Pro
NM_000457.6:c.758G>C	NP_000448.3:p.Arg253Pro
NM_001287183.2:c.683G>C	NP_001274112.1:p.Arg228Pro
NM_175914.5:c.692G>C MANE Select	NP_787110.2:p.Arg231Pro