Canonical Allele Identifier: CA510582607

Gene: HNF4A

Linked Data

• MyVariant Identifiers: chr20:g.43042374A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44413734A>C , CM000682.2:g.44413734A>C	GRCh38
NC_000020.10:g.43042374A>C , CM000682.1:g.43042374A>C	GRCh37
NC_000020.9:g.42475788A>C	NCBI36
NG_009818.1:g.62934A>C , LRG_483:g.62934A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316673.9:c.360A>C MANE Select	ENSP00000315180.4:p.Ser120=
ENST00000316099.10:c.426A>C	ENSP00000312987.3:p.Ser142=
ENST00000619550.5:c.400A>C
ENST00000683148.1:n.402A>C
ENST00000683657.1:n.1550A>C
ENST00000316099.9:c.426A>C	ENSP00000312987.3:p.Ser142=
ENST00000316099.8:c.426A>C	ENSP00000312987.3:p.Ser142=
ENST00000316673.8:c.360A>C	ENSP00000315180.4:p.Ser120=
ENST00000372920.1:c.*193A>C	ENSP00000362011.1:n.*193A>C
ENST00000415691.2:c.426A>C	ENSP00000412111.1:p.Ser142=
ENST00000443598.6:c.426A>C	ENSP00000410911.2:p.Ser142=
ENST00000457232.5:c.360A>C	ENSP00000396216.1:p.Ser120=
ENST00000609795.5:c.360A>C	ENSP00000476609.1:p.Ser120=
ENST00000619550.4:c.351A>C	ENSP00000481331.1:p.Ser117=
NM_000457.4:c.426A>C , LRG_483t2:c.426A>C	NP_000448.3:p.Ser142=
NM_001030003.2:c.360A>C	NP_001025174.1:p.Ser120=
NM_001030004.2:c.360A>C	NP_001025175.1:p.Ser120=
NM_001258355.1:c.405A>C	NP_001245284.1:p.Ser135=
NM_001287182.1:c.351A>C	NP_001274111.1:p.Ser117=
NM_001287183.1:c.351A>C , LRG_483t3:c.351A>C	NP_001274112.1:p.Ser117=
NM_001287184.1:c.351A>C	NP_001274113.1:p.Ser117=
NM_175914.4:c.360A>C , LRG_483t1:c.360A>C	NP_787110.2:p.Ser120=
NM_178849.2:c.426A>C	NP_849180.1:p.Ser142=
NM_178850.2:c.426A>C	NP_849181.1:p.Ser142=
XM_005260407.2:c.543A>C	XP_005260464.1:p.Ser181=
XM_011528797.1:c.474A>C	XP_011527099.1:p.Ser158=
XM_011528798.1:c.474A>C	XP_011527100.1:p.Ser158=
XM_005260407.4:c.543A>C	XP_005260464.1:p.Ser181=
NM_001030003.3:c.360A>C	NP_001025174.1:p.Ser120=
NM_001030004.3:c.360A>C	NP_001025175.1:p.Ser120=
NM_001258355.2:c.405A>C	NP_001245284.1:p.Ser135=
NM_001287182.2:c.351A>C	NP_001274111.1:p.Ser117=
NM_001287184.2:c.351A>C	NP_001274113.1:p.Ser117=
NM_178849.3:c.426A>C	NP_849180.1:p.Ser142=
NM_178850.3:c.426A>C	NP_849181.1:p.Ser142=
NM_000457.5:c.426A>C	NP_000448.3:p.Ser142=
NM_000457.6:c.426A>C	NP_000448.3:p.Ser142=
NM_001287183.2:c.351A>C	NP_001274112.1:p.Ser117=
NM_175914.5:c.360A>C MANE Select	NP_787110.2:p.Ser120=