Canonical Allele Identifier: CA407183619

Gene: PPP2R1A

Linked Data

• dbSNP Id: rs2122334970
• MyVariant Identifiers: chr19:g.52715992C>T (hg19) ; chr19:g.52212739C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52212739C>T , CM000681.2:g.52212739C>T	GRCh38
NC_000019.9:g.52715992C>T , CM000681.1:g.52715992C>T	GRCh37
NC_000019.8:g.57407804C>T	NCBI36
NG_047068.1:g.27938C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000454220.7:c.677C>T	ENSP00000391905.3:p.Ala226Val
ENST00000703395.1:c.20C>T	ENSP00000515286.1:p.Ala7Val
ENST00000703396.1:n.501C>T
ENST00000703397.1:c.20C>T	ENSP00000515287.1:p.Ala7Val
ENST00000703398.1:c.599C>T	ENSP00000515288.1:p.Ala200Val
ENST00000703421.1:n.710C>T
ENST00000703422.1:c.533C>T	ENSP00000515292.1:p.Ala178Val
ENST00000703423.1:c.20C>T	ENSP00000515293.1:p.Ala7Val
ENST00000322088.11:c.557C>T MANE Select	ENSP00000324804.6:p.Ala186Val
ENST00000322088.10:c.557C>T	ENSP00000324804.6:p.Ala186Val
ENST00000454220.6:c.677C>T	ENSP00000391905.2:p.Ala226Val
ENST00000462047.1:n.248C>T
ENST00000462990.5:c.20C>T	ENSP00000470504.1:p.Ala7Val
NM_014225.5:c.557C>T	NP_055040.2:p.Ala186Val
NR_033500.1:n.751C>T
NM_001363656.1:c.20C>T	NP_001350585.1:p.Ala7Val
NM_014225.6:c.557C>T MANE Select	NP_055040.2:p.Ala186Val
NM_001363656.2:c.20C>T	NP_001350585.1:p.Ala7Val
NR_033500.2:n.501C>T