Canonical Allele Identifier: CA407183609

Gene: PPP2R1A

Linked Data

• dbSNP Id: rs2122334945
• MyVariant Identifiers: chr19:g.52715991G>A (hg19) ; chr19:g.52212738G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52212738G>A , CM000681.2:g.52212738G>A	GRCh38
NC_000019.9:g.52715991G>A , CM000681.1:g.52715991G>A	GRCh37
NC_000019.8:g.57407803G>A	NCBI36
NG_047068.1:g.27937G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454220.7:c.676G>A	ENSP00000391905.3:p.Ala226Thr
ENST00000703395.1:c.19G>A	ENSP00000515286.1:p.Ala7Thr
ENST00000703396.1:n.500G>A
ENST00000703397.1:c.19G>A	ENSP00000515287.1:p.Ala7Thr
ENST00000703398.1:c.598G>A	ENSP00000515288.1:p.Ala200Thr
ENST00000703421.1:n.709G>A
ENST00000703422.1:c.532G>A	ENSP00000515292.1:p.Ala178Thr
ENST00000703423.1:c.19G>A	ENSP00000515293.1:p.Ala7Thr
ENST00000322088.11:c.556G>A MANE Select	ENSP00000324804.6:p.Ala186Thr
ENST00000322088.10:c.556G>A	ENSP00000324804.6:p.Ala186Thr
ENST00000454220.6:c.676G>A	ENSP00000391905.2:p.Ala226Thr
ENST00000462047.1:n.247G>A
ENST00000462990.5:c.19G>A	ENSP00000470504.1:p.Ala7Thr
NM_014225.5:c.556G>A	NP_055040.2:p.Ala186Thr
NR_033500.1:n.750G>A
NM_001363656.1:c.19G>A	NP_001350585.1:p.Ala7Thr
NM_014225.6:c.556G>A MANE Select	NP_055040.2:p.Ala186Thr
NM_001363656.2:c.19G>A	NP_001350585.1:p.Ala7Thr
NR_033500.2:n.500G>A