Canonical Allele Identifier: CA508826397

Gene: PPP2R1A

Linked Data

• dbSNP Id: rs2122334459
• MyVariant Identifiers: chr19:g.52715960A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52212707A>G , CM000681.2:g.52212707A>G	GRCh38
NC_000019.9:g.52715960A>G , CM000681.1:g.52715960A>G	GRCh37
NC_000019.8:g.57407772A>G	NCBI36
NG_047068.1:g.27906A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454220.7:c.645A>G	ENSP00000391905.3:p.Ser215=
ENST00000703395.1:c.-13A>G	ENSP00000515286.1:n.-13A>G
ENST00000703396.1:n.469A>G
ENST00000703397.1:c.-13A>G	ENSP00000515287.1:n.-13A>G
ENST00000703398.1:c.567A>G	ENSP00000515288.1:p.Ser189=
ENST00000703421.1:n.678A>G
ENST00000703422.1:c.501A>G	ENSP00000515292.1:p.Ser167=
ENST00000703423.1:c.-13A>G	ENSP00000515293.1:n.-13A>G
ENST00000322088.11:c.525A>G MANE Select	ENSP00000324804.6:p.Ser175=
ENST00000322088.10:c.525A>G	ENSP00000324804.6:p.Ser175=
ENST00000454220.6:c.645A>G	ENSP00000391905.2:p.Ser215=
ENST00000462047.1:n.216A>G
ENST00000462990.5:c.-13A>G	ENSP00000470504.1:n.-13A>G
NM_014225.5:c.525A>G	NP_055040.2:p.Ser175=
NR_033500.1:n.719A>G
NM_001363656.1:c.-13A>G	NP_001350585.1:n.-13A>G
NM_014225.6:c.525A>G MANE Select	NP_055040.2:p.Ser175=
NM_001363656.2:c.-13A>G	NP_001350585.1:n.-13A>G
NR_033500.2:n.469A>G