Canonical Allele Identifier: CA2341739294
Gene: PPP2R1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.52212737A= , CM000681.2:g.52212737A= GRCh38
NC_000019.9:g.52715990A= , CM000681.1:g.52715990A= GRCh37
NC_000019.8:g.57407802A= NCBI36
NG_047068.1:g.27936A=

Transcript Alleles

HGVS Amino-acid change
ENST00000454220.7:c.675A= ENSP00000391905.3:p.Ala225=
ENST00000703395.1:c.18A= ENSP00000515286.1:p.Ala6=
ENST00000703396.1:n.499A=
ENST00000703397.1:c.18A= ENSP00000515287.1:p.Ala6=
ENST00000703398.1:c.597A= ENSP00000515288.1:p.Ala199=
ENST00000703421.1:n.708A=
ENST00000703422.1:c.531A= ENSP00000515292.1:p.Ala177=
ENST00000703423.1:c.18A= ENSP00000515293.1:p.Ala6=
ENST00000322088.11:c.555A= MANE Select ENSP00000324804.6:p.Ala185=
ENST00000322088.10:c.555A= ENSP00000324804.6:p.Ala185=
ENST00000454220.6:c.675A= ENSP00000391905.2:p.Ala225=
ENST00000462047.1:n.246A=
ENST00000462990.5:c.18A= ENSP00000470504.1:p.Ala6=
NM_014225.5:c.555A= NP_055040.2:p.Ala185=
NR_033500.1:n.749A=
NM_001363656.1:c.18A= NP_001350585.1:p.Ala6=
NM_014225.6:c.555A= MANE Select NP_055040.2:p.Ala185=
NM_001363656.2:c.18A= NP_001350585.1:p.Ala6=
NR_033500.2:n.499A=