Canonical Allele Identifier: CA2341739283

Gene: PPP2R1A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52212716C= , CM000681.2:g.52212716C=	GRCh38
NC_000019.9:g.52715969C= , CM000681.1:g.52715969C=	GRCh37
NC_000019.8:g.57407781C=	NCBI36
NG_047068.1:g.27915C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454220.7:c.654C=	ENSP00000391905.3:p.Thr218=
ENST00000703395.1:c.-4C=	ENSP00000515286.1:n.-4C=
ENST00000703396.1:n.478C=
ENST00000703397.1:c.-4C=	ENSP00000515287.1:n.-4C=
ENST00000703398.1:c.576C=	ENSP00000515288.1:p.Thr192=
ENST00000703421.1:n.687C=
ENST00000703422.1:c.510C=	ENSP00000515292.1:p.Thr170=
ENST00000703423.1:c.-4C=	ENSP00000515293.1:n.-4C=
ENST00000322088.11:c.534C= MANE Select	ENSP00000324804.6:p.Thr178=
ENST00000322088.10:c.534C=	ENSP00000324804.6:p.Thr178=
ENST00000454220.6:c.654C=	ENSP00000391905.2:p.Thr218=
ENST00000462047.1:n.225C=
ENST00000462990.5:c.-4C=	ENSP00000470504.1:n.-4C=
NM_014225.5:c.534C=	NP_055040.2:p.Thr178=
NR_033500.1:n.728C=
NM_001363656.1:c.-4C=	NP_001350585.1:n.-4C=
NM_014225.6:c.534C= MANE Select	NP_055040.2:p.Thr178=
NM_001363656.2:c.-4C=	NP_001350585.1:n.-4C=
NR_033500.2:n.478C=