Canonical Allele Identifier: CA407183630
Gene: PPP2R1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.52212742C>G , CM000681.2:g.52212742C>G GRCh38
NC_000019.9:g.52715995C>G , CM000681.1:g.52715995C>G GRCh37
NC_000019.8:g.57407807C>G NCBI36
NG_047068.1:g.27941C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000454220.7:c.680C>G ENSP00000391905.3:p.Ser227Cys
ENST00000703395.1:c.23C>G ENSP00000515286.1:p.Ser8Cys
ENST00000703396.1:n.504C>G
ENST00000703397.1:c.23C>G ENSP00000515287.1:p.Ser8Cys
ENST00000703398.1:c.602C>G ENSP00000515288.1:p.Ser201Cys
ENST00000703421.1:n.713C>G
ENST00000703422.1:c.536C>G ENSP00000515292.1:p.Ser179Cys
ENST00000703423.1:c.23C>G ENSP00000515293.1:p.Ser8Cys
ENST00000322088.11:c.560C>G MANE Select ENSP00000324804.6:p.Ser187Cys
ENST00000322088.10:c.560C>G ENSP00000324804.6:p.Ser187Cys
ENST00000454220.6:c.680C>G ENSP00000391905.2:p.Ser227Cys
ENST00000462047.1:n.251C>G
ENST00000462990.5:c.23C>G ENSP00000470504.1:p.Ser8Cys
NM_014225.5:c.560C>G NP_055040.2:p.Ser187Cys
NR_033500.1:n.754C>G
NM_001363656.1:c.23C>G NP_001350585.1:p.Ser8Cys
NM_014225.6:c.560C>G MANE Select NP_055040.2:p.Ser187Cys
NM_001363656.2:c.23C>G NP_001350585.1:p.Ser8Cys
NR_033500.2:n.504C>G