Canonical Allele Identifier: CA2341728206

Gene: PPP2R1A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52190183G= , CM000681.2:g.52190183G=	GRCh38
NC_000019.9:g.52693436G= , CM000681.1:g.52693436G=	GRCh37
NC_000019.8:g.57385248G=	NCBI36
NG_047068.1:g.5382G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454220.7:c.87G=	ENSP00000391905.3:p.Arg29=
ENST00000703395.1:c.-459-11761G=	ENSP00000515286.1:n.-459-11761G=
ENST00000703396.1:n.123+9G=
ENST00000703397.1:c.-657+9G=	ENSP00000515287.1:n.-657+9G=
ENST00000703398.1:c.78+9G=	ENSP00000515288.1:n.78+9G=
ENST00000703421.1:n.231+1027G=
ENST00000703422.1:c.78+9G=	ENSP00000515292.1:n.78+9G=
ENST00000322088.11:c.78+9G= MANE Select	ENSP00000324804.6:n.78+9G=
ENST00000322088.10:c.78+9G=	ENSP00000324804.6:n.78+9G=
ENST00000454220.6:c.87G=	ENSP00000391905.2:p.Arg29=
ENST00000468280.5:n.61+9G=
ENST00000477989.1:c.78+9G=	ENSP00000471298.1:n.78+9G=
ENST00000490868.5:c.78+9G=	ENSP00000469150.1:n.78+9G=
ENST00000628959.1:c.78+9G=	ENSP00000485914.1:n.78+9G=
NM_014225.5:c.78+9G=	NP_055040.2:n.78+9G=
NR_033500.1:n.373+9G=
NM_014225.6:c.78+9G= MANE Select	NP_055040.2:n.78+9G=
NR_033500.2:n.123+9G=