Canonical Allele Identifier: CA9621323

Gene: PPP2R1A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52211367G>A , CM000681.2:g.52211367G>A	GRCh38
NC_000019.9:g.52714620G>A , CM000681.1:g.52714620G>A	GRCh37
NC_000019.8:g.57406432G>A	NCBI36
NG_047068.1:g.26566G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_014225.6:c.378G>A MANE Select	NP_055040.2:p.Ala126=
ENST00000322088.11:c.378G>A MANE Select	ENSP00000324804.6:p.Ala126=
NM_001363656.1:c.-160G>A	NP_001350585.1:n.-160G>A
NM_001363656.2:c.-160G>A	NP_001350585.1:n.-160G>A
NM_014225.5:c.378G>A	NP_055040.2:p.Ala126=
NR_033500.1:n.572G>A
NR_033500.2:n.322G>A
ENST00000322088.10:c.378G>A	ENSP00000324804.6:p.Ala126=
ENST00000454220.6:c.498G>A	ENSP00000391905.2:p.Ala166=
ENST00000454220.7:c.498G>A	ENSP00000391905.3:p.Ala166=
ENST00000462990.5:c.-160G>A	ENSP00000470504.1:n.-160G>A
ENST00000468280.5:n.361G>A
ENST00000473455.2:n.477G>A
ENST00000490868.5:c.*386G>A	ENSP00000469150.1:n.*386G>A
ENST00000703395.1:c.-160G>A	ENSP00000515286.1:n.-160G>A
ENST00000703396.1:n.322G>A
ENST00000703397.1:c.-160G>A	ENSP00000515287.1:n.-160G>A
ENST00000703398.1:c.420G>A	ENSP00000515288.1:p.Ala140=
ENST00000703421.1:n.531G>A
ENST00000703422.1:c.354G>A	ENSP00000515292.1:p.Ala118=
ENST00000703423.1:c.-160G>A	ENSP00000515293.1:n.-160G>A