Canonical Allele Identifier: CA508826425

Gene: PPP2R1A

Linked Data

• dbSNP Id: rs2122335020
• MyVariant Identifiers: chr19:g.52715996C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52212743C>T , CM000681.2:g.52212743C>T	GRCh38
NC_000019.9:g.52715996C>T , CM000681.1:g.52715996C>T	GRCh37
NC_000019.8:g.57407808C>T	NCBI36
NG_047068.1:g.27942C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454220.7:c.681C>T	ENSP00000391905.3:p.Ser227=
ENST00000703395.1:c.24C>T	ENSP00000515286.1:p.Ser8=
ENST00000703396.1:n.505C>T
ENST00000703397.1:c.24C>T	ENSP00000515287.1:p.Ser8=
ENST00000703398.1:c.603C>T	ENSP00000515288.1:p.Ser201=
ENST00000703421.1:n.714C>T
ENST00000703422.1:c.537C>T	ENSP00000515292.1:p.Ser179=
ENST00000703423.1:c.24C>T	ENSP00000515293.1:p.Ser8=
ENST00000322088.11:c.561C>T MANE Select	ENSP00000324804.6:p.Ser187=
ENST00000322088.10:c.561C>T	ENSP00000324804.6:p.Ser187=
ENST00000454220.6:c.681C>T	ENSP00000391905.2:p.Ser227=
ENST00000462047.1:n.252C>T
ENST00000462990.5:c.24C>T	ENSP00000470504.1:p.Ser8=
NM_014225.5:c.561C>T	NP_055040.2:p.Ser187=
NR_033500.1:n.755C>T
NM_001363656.1:c.24C>T	NP_001350585.1:p.Ser8=
NM_014225.6:c.561C>T MANE Select	NP_055040.2:p.Ser187=
NM_001363656.2:c.24C>T	NP_001350585.1:p.Ser8=
NR_033500.2:n.505C>T