Canonical Allele Identifier: CA407183363

Gene: PPP2R1A

Linked Data

• dbSNP Id: rs2122334232
• MyVariant Identifiers: chr19:g.52715943T>A (hg19) ; chr19:g.52212690T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52212690T>A , CM000681.2:g.52212690T>A	GRCh38
NC_000019.9:g.52715943T>A , CM000681.1:g.52715943T>A	GRCh37
NC_000019.8:g.57407755T>A	NCBI36
NG_047068.1:g.27889T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454220.7:c.628T>A	ENSP00000391905.3:p.Phe210Ile
ENST00000703395.1:c.-30T>A	ENSP00000515286.1:n.-30T>A
ENST00000703396.1:n.452T>A
ENST00000703397.1:c.-30T>A	ENSP00000515287.1:n.-30T>A
ENST00000703398.1:c.550T>A	ENSP00000515288.1:p.Phe184Ile
ENST00000703421.1:n.661T>A
ENST00000703422.1:c.484T>A	ENSP00000515292.1:p.Phe162Ile
ENST00000703423.1:c.-30T>A	ENSP00000515293.1:n.-30T>A
ENST00000322088.11:c.508T>A MANE Select	ENSP00000324804.6:p.Phe170Ile
ENST00000322088.10:c.508T>A	ENSP00000324804.6:p.Phe170Ile
ENST00000454220.6:c.628T>A	ENSP00000391905.2:p.Phe210Ile
ENST00000462047.1:n.199T>A
ENST00000462990.5:c.-30T>A	ENSP00000470504.1:n.-30T>A
ENST00000473455.2:n.607T>A
NM_014225.5:c.508T>A	NP_055040.2:p.Phe170Ile
NR_033500.1:n.702T>A
NM_001363656.1:c.-30T>A	NP_001350585.1:n.-30T>A
NM_014225.6:c.508T>A MANE Select	NP_055040.2:p.Phe170Ile
NM_001363656.2:c.-30T>A	NP_001350585.1:n.-30T>A
NR_033500.2:n.452T>A