Canonical Allele Identifier: CA2341739250

Gene: PPP2R1A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52212620G= , CM000681.2:g.52212620G=	GRCh38
NC_000019.9:g.52715873G= , CM000681.1:g.52715873G=	GRCh37
NC_000019.8:g.57407685G=	NCBI36
NG_047068.1:g.27819G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454220.7:c.624-66G=	ENSP00000391905.3:n.624-66G=
ENST00000703395.1:c.-34-66G=	ENSP00000515286.1:n.-34-66G=
ENST00000703396.1:n.448-66G=
ENST00000703397.1:c.-34-66G=	ENSP00000515287.1:n.-34-66G=
ENST00000703398.1:c.546-66G=	ENSP00000515288.1:n.546-66G=
ENST00000703421.1:n.657-66G=
ENST00000703422.1:c.480-66G=	ENSP00000515292.1:n.480-66G=
ENST00000703423.1:c.-34-66G=	ENSP00000515293.1:n.-34-66G=
ENST00000322088.11:c.504-66G= MANE Select	ENSP00000324804.6:n.504-66G=
ENST00000322088.10:c.504-66G=	ENSP00000324804.6:n.504-66G=
ENST00000454220.6:c.624-66G=	ENSP00000391905.2:n.624-66G=
ENST00000462047.1:n.129G=
ENST00000462990.5:c.-34-66G=	ENSP00000470504.1:n.-34-66G=
ENST00000473455.2:n.603-66G=
NM_014225.5:c.504-66G=	NP_055040.2:n.504-66G=
NR_033500.1:n.698-66G=
NM_001363656.1:c.-34-66G=	NP_001350585.1:n.-34-66G=
NM_014225.6:c.504-66G= MANE Select	NP_055040.2:n.504-66G=
NM_001363656.2:c.-34-66G=	NP_001350585.1:n.-34-66G=
NR_033500.2:n.448-66G=