Canonical Allele Identifier: CA407184059

Gene: PPP2R1A

Linked Data

• dbSNP Id: rs201263415
• MyVariant Identifiers: chr19:g.52716067A>C (hg19) ; chr19:g.52212814A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52212814A>C , CM000681.2:g.52212814A>C	GRCh38
NC_000019.9:g.52716067A>C , CM000681.1:g.52716067A>C	GRCh37
NC_000019.8:g.57407879A>C	NCBI36
NG_047068.1:g.28013A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454220.7:c.752A>C	ENSP00000391905.3:p.Asn251Thr
ENST00000703395.1:c.95A>C	ENSP00000515286.1:p.Asn32Thr
ENST00000703396.1:n.576A>C
ENST00000703397.1:c.95A>C	ENSP00000515287.1:p.Asn32Thr
ENST00000703398.1:c.674A>C	ENSP00000515288.1:p.Asn225Thr
ENST00000703421.1:n.785A>C
ENST00000703422.1:c.608A>C	ENSP00000515292.1:p.Asn203Thr
ENST00000703423.1:c.95A>C	ENSP00000515293.1:p.Asn32Thr
ENST00000322088.11:c.632A>C MANE Select	ENSP00000324804.6:p.Asn211Thr
ENST00000322088.10:c.632A>C	ENSP00000324804.6:p.Asn211Thr
ENST00000454220.6:c.752A>C	ENSP00000391905.2:p.Asn251Thr
ENST00000462047.1:n.323A>C
ENST00000462990.5:c.95A>C	ENSP00000470504.1:p.Asn32Thr
NM_014225.5:c.632A>C	NP_055040.2:p.Asn211Thr
NR_033500.1:n.826A>C
NM_001363656.1:c.95A>C	NP_001350585.1:p.Asn32Thr
NM_014225.6:c.632A>C MANE Select	NP_055040.2:p.Asn211Thr
NM_001363656.2:c.95A>C	NP_001350585.1:p.Asn32Thr
NR_033500.2:n.576A>C