Canonical Allele Identifier: CA508826489

Gene: PPP2R1A

Linked Data

• MyVariant Identifiers: chr19:g.52716065C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52212812C>A , CM000681.2:g.52212812C>A	GRCh38
NC_000019.9:g.52716065C>A , CM000681.1:g.52716065C>A	GRCh37
NC_000019.8:g.57407877C>A	NCBI36
NG_047068.1:g.28011C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454220.7:c.750C>A	ENSP00000391905.3:p.Ser250=
ENST00000703395.1:c.93C>A	ENSP00000515286.1:p.Ser31=
ENST00000703396.1:n.574C>A
ENST00000703397.1:c.93C>A	ENSP00000515287.1:p.Ser31=
ENST00000703398.1:c.672C>A	ENSP00000515288.1:p.Ser224=
ENST00000703421.1:n.783C>A
ENST00000703422.1:c.606C>A	ENSP00000515292.1:p.Ser202=
ENST00000703423.1:c.93C>A	ENSP00000515293.1:p.Ser31=
ENST00000322088.11:c.630C>A MANE Select	ENSP00000324804.6:p.Ser210=
ENST00000322088.10:c.630C>A	ENSP00000324804.6:p.Ser210=
ENST00000454220.6:c.750C>A	ENSP00000391905.2:p.Ser250=
ENST00000462047.1:n.321C>A
ENST00000462990.5:c.93C>A	ENSP00000470504.1:p.Ser31=
NM_014225.5:c.630C>A	NP_055040.2:p.Ser210=
NR_033500.1:n.824C>A
NM_001363656.1:c.93C>A	NP_001350585.1:p.Ser31=
NM_014225.6:c.630C>A MANE Select	NP_055040.2:p.Ser210=
NM_001363656.2:c.93C>A	NP_001350585.1:p.Ser31=
NR_033500.2:n.574C>A