Canonical Allele Identifier: CA2341739292

Gene: PPP2R1A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52212734C= , CM000681.2:g.52212734C=	GRCh38
NC_000019.9:g.52715987C= , CM000681.1:g.52715987C=	GRCh37
NC_000019.8:g.57407799C=	NCBI36
NG_047068.1:g.27933C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454220.7:c.672C=	ENSP00000391905.3:p.Ala224=
ENST00000703395.1:c.15C=	ENSP00000515286.1:p.Ala5=
ENST00000703396.1:n.496C=
ENST00000703397.1:c.15C=	ENSP00000515287.1:p.Ala5=
ENST00000703398.1:c.594C=	ENSP00000515288.1:p.Ala198=
ENST00000703421.1:n.705C=
ENST00000703422.1:c.528C=	ENSP00000515292.1:p.Ala176=
ENST00000703423.1:c.15C=	ENSP00000515293.1:p.Ala5=
ENST00000322088.11:c.552C= MANE Select	ENSP00000324804.6:p.Ala184=
ENST00000322088.10:c.552C=	ENSP00000324804.6:p.Ala184=
ENST00000454220.6:c.672C=	ENSP00000391905.2:p.Ala224=
ENST00000462047.1:n.243C=
ENST00000462990.5:c.15C=	ENSP00000470504.1:p.Ala5=
NM_014225.5:c.552C=	NP_055040.2:p.Ala184=
NR_033500.1:n.746C=
NM_001363656.1:c.15C=	NP_001350585.1:p.Ala5=
NM_014225.6:c.552C= MANE Select	NP_055040.2:p.Ala184=
NM_001363656.2:c.15C=	NP_001350585.1:p.Ala5=
NR_033500.2:n.496C=