Canonical Allele Identifier: CA2341739274

Gene: PPP2R1A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52212687T= , CM000681.2:g.52212687T=	GRCh38
NC_000019.9:g.52715940T= , CM000681.1:g.52715940T=	GRCh37
NC_000019.8:g.57407752T=	NCBI36
NG_047068.1:g.27886T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454220.7:c.625T=	ENSP00000391905.3:p.Tyr209=
ENST00000703395.1:c.-33T=	ENSP00000515286.1:n.-33T=
ENST00000703396.1:n.449T=
ENST00000703397.1:c.-33T=	ENSP00000515287.1:n.-33T=
ENST00000703398.1:c.547T=	ENSP00000515288.1:p.Tyr183=
ENST00000703421.1:n.658T=
ENST00000703422.1:c.481T=	ENSP00000515292.1:p.Tyr161=
ENST00000703423.1:c.-33T=	ENSP00000515293.1:n.-33T=
ENST00000322088.11:c.505T= MANE Select	ENSP00000324804.6:p.Tyr169=
ENST00000322088.10:c.505T=	ENSP00000324804.6:p.Tyr169=
ENST00000454220.6:c.625T=	ENSP00000391905.2:p.Tyr209=
ENST00000462047.1:n.196T=
ENST00000462990.5:c.-33T=	ENSP00000470504.1:n.-33T=
ENST00000473455.2:n.604T=
NM_014225.5:c.505T=	NP_055040.2:p.Tyr169=
NR_033500.1:n.699T=
NM_001363656.1:c.-33T=	NP_001350585.1:n.-33T=
NM_014225.6:c.505T= MANE Select	NP_055040.2:p.Tyr169=
NM_001363656.2:c.-33T=	NP_001350585.1:n.-33T=
NR_033500.2:n.449T=