Canonical Allele Identifier: CA407183503

Gene: PPP2R1A

Linked Data

• MyVariant Identifiers: chr19:g.52715970C>A (hg19) ; chr19:g.52212717C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52212717C>A , CM000681.2:g.52212717C>A	GRCh38
NC_000019.9:g.52715970C>A , CM000681.1:g.52715970C>A	GRCh37
NC_000019.8:g.57407782C>A	NCBI36
NG_047068.1:g.27916C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454220.7:c.655C>A	ENSP00000391905.3:p.Pro219Thr
ENST00000703395.1:c.-3C>A	ENSP00000515286.1:n.-3C>A
ENST00000703396.1:n.479C>A
ENST00000703397.1:c.-3C>A	ENSP00000515287.1:n.-3C>A
ENST00000703398.1:c.577C>A	ENSP00000515288.1:p.Pro193Thr
ENST00000703421.1:n.688C>A
ENST00000703422.1:c.511C>A	ENSP00000515292.1:p.Pro171Thr
ENST00000703423.1:c.-3C>A	ENSP00000515293.1:n.-3C>A
ENST00000322088.11:c.535C>A MANE Select	ENSP00000324804.6:p.Pro179Thr
ENST00000322088.10:c.535C>A	ENSP00000324804.6:p.Pro179Thr
ENST00000454220.6:c.655C>A	ENSP00000391905.2:p.Pro219Thr
ENST00000462047.1:n.226C>A
ENST00000462990.5:c.-3C>A	ENSP00000470504.1:n.-3C>A
NM_014225.5:c.535C>A	NP_055040.2:p.Pro179Thr
NR_033500.1:n.729C>A
NM_001363656.1:c.-3C>A	NP_001350585.1:n.-3C>A
NM_014225.6:c.535C>A MANE Select	NP_055040.2:p.Pro179Thr
NM_001363656.2:c.-3C>A	NP_001350585.1:n.-3C>A
NR_033500.2:n.479C>A