Canonical Allele Identifier: CA2341739290

Gene: PPP2R1A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52212730G= , CM000681.2:g.52212730G=	GRCh38
NC_000019.9:g.52715983G= , CM000681.1:g.52715983G=	GRCh37
NC_000019.8:g.57407795G=	NCBI36
NG_047068.1:g.27929G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454220.7:c.668G=	ENSP00000391905.3:p.Arg223=
ENST00000703395.1:c.11G=	ENSP00000515286.1:p.Arg4=
ENST00000703396.1:n.492G=
ENST00000703397.1:c.11G=	ENSP00000515287.1:p.Arg4=
ENST00000703398.1:c.590G=	ENSP00000515288.1:p.Arg197=
ENST00000703421.1:n.701G=
ENST00000703422.1:c.524G=	ENSP00000515292.1:p.Arg175=
ENST00000703423.1:c.11G=	ENSP00000515293.1:p.Arg4=
ENST00000322088.11:c.548G= MANE Select	ENSP00000324804.6:p.Arg183=
ENST00000322088.10:c.548G=	ENSP00000324804.6:p.Arg183=
ENST00000454220.6:c.668G=	ENSP00000391905.2:p.Arg223=
ENST00000462047.1:n.239G=
ENST00000462990.5:c.11G=	ENSP00000470504.1:p.Arg4=
NM_014225.5:c.548G=	NP_055040.2:p.Arg183=
NR_033500.1:n.742G=
NM_001363656.1:c.11G=	NP_001350585.1:p.Arg4=
NM_014225.6:c.548G= MANE Select	NP_055040.2:p.Arg183=
NM_001363656.2:c.11G=	NP_001350585.1:p.Arg4=
NR_033500.2:n.492G=