Canonical Allele Identifier: CA508826384

Gene: PPP2R1A

Linked Data

• MyVariant Identifiers: chr19:g.52715945C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52212692C>T , CM000681.2:g.52212692C>T	GRCh38
NC_000019.9:g.52715945C>T , CM000681.1:g.52715945C>T	GRCh37
NC_000019.8:g.57407757C>T	NCBI36
NG_047068.1:g.27891C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454220.7:c.630C>T	ENSP00000391905.3:p.Phe210=
ENST00000703395.1:c.-28C>T	ENSP00000515286.1:n.-28C>T
ENST00000703396.1:n.454C>T
ENST00000703397.1:c.-28C>T	ENSP00000515287.1:n.-28C>T
ENST00000703398.1:c.552C>T	ENSP00000515288.1:p.Phe184=
ENST00000703421.1:n.663C>T
ENST00000703422.1:c.486C>T	ENSP00000515292.1:p.Phe162=
ENST00000703423.1:c.-28C>T	ENSP00000515293.1:n.-28C>T
ENST00000322088.11:c.510C>T MANE Select	ENSP00000324804.6:p.Phe170=
ENST00000322088.10:c.510C>T	ENSP00000324804.6:p.Phe170=
ENST00000454220.6:c.630C>T	ENSP00000391905.2:p.Phe210=
ENST00000462047.1:n.201C>T
ENST00000462990.5:c.-28C>T	ENSP00000470504.1:n.-28C>T
ENST00000473455.2:n.609C>T
NM_014225.5:c.510C>T	NP_055040.2:p.Phe170=
NR_033500.1:n.704C>T
NM_001363656.1:c.-28C>T	NP_001350585.1:n.-28C>T
NM_014225.6:c.510C>T MANE Select	NP_055040.2:p.Phe170=
NM_001363656.2:c.-28C>T	NP_001350585.1:n.-28C>T
NR_033500.2:n.454C>T