Canonical Allele Identifier: CA2341739281

Gene: PPP2R1A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52212701G= , CM000681.2:g.52212701G=	GRCh38
NC_000019.9:g.52715954G= , CM000681.1:g.52715954G=	GRCh37
NC_000019.8:g.57407766G=	NCBI36
NG_047068.1:g.27900G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454220.7:c.639G=	ENSP00000391905.3:p.Leu213=
ENST00000703395.1:c.-19G=	ENSP00000515286.1:n.-19G=
ENST00000703396.1:n.463G=
ENST00000703397.1:c.-19G=	ENSP00000515287.1:n.-19G=
ENST00000703398.1:c.561G=	ENSP00000515288.1:p.Leu187=
ENST00000703421.1:n.672G=
ENST00000703422.1:c.495G=	ENSP00000515292.1:p.Leu165=
ENST00000703423.1:c.-19G=	ENSP00000515293.1:n.-19G=
ENST00000322088.11:c.519G= MANE Select	ENSP00000324804.6:p.Leu173=
ENST00000322088.10:c.519G=	ENSP00000324804.6:p.Leu173=
ENST00000454220.6:c.639G=	ENSP00000391905.2:p.Leu213=
ENST00000462047.1:n.210G=
ENST00000462990.5:c.-19G=	ENSP00000470504.1:n.-19G=
NM_014225.5:c.519G=	NP_055040.2:p.Leu173=
NR_033500.1:n.713G=
NM_001363656.1:c.-19G=	NP_001350585.1:n.-19G=
NM_014225.6:c.519G= MANE Select	NP_055040.2:p.Leu173=
NM_001363656.2:c.-19G=	NP_001350585.1:n.-19G=
NR_033500.2:n.463G=