Canonical Allele Identifier: CA2735969824
Gene: PPP2R1A HGNC NCBI

Linked Data

dbSNP Id: rs2122333687

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.52212627T>G , CM000681.2:g.52212627T>G GRCh38
NC_000019.9:g.52715880T>G , CM000681.1:g.52715880T>G GRCh37
NC_000019.8:g.57407692T>G NCBI36
NG_047068.1:g.27826T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000454220.7:c.624-59T>G ENSP00000391905.3:n.624-59T>G
ENST00000703395.1:c.-34-59T>G ENSP00000515286.1:n.-34-59T>G
ENST00000703396.1:n.448-59T>G
ENST00000703397.1:c.-34-59T>G ENSP00000515287.1:n.-34-59T>G
ENST00000703398.1:c.546-59T>G ENSP00000515288.1:n.546-59T>G
ENST00000703421.1:n.657-59T>G
ENST00000703422.1:c.480-59T>G ENSP00000515292.1:n.480-59T>G
ENST00000703423.1:c.-34-59T>G ENSP00000515293.1:n.-34-59T>G
ENST00000322088.11:c.504-59T>G MANE Select ENSP00000324804.6:n.504-59T>G
ENST00000322088.10:c.504-59T>G ENSP00000324804.6:n.504-59T>G
ENST00000454220.6:c.624-59T>G ENSP00000391905.2:n.624-59T>G
ENST00000462047.1:n.136T>G
ENST00000462990.5:c.-34-59T>G ENSP00000470504.1:n.-34-59T>G
ENST00000473455.2:n.603-59T>G
NM_014225.5:c.504-59T>G NP_055040.2:n.504-59T>G
NR_033500.1:n.698-59T>G
NM_001363656.1:c.-34-59T>G NP_001350585.1:n.-34-59T>G
NM_014225.6:c.504-59T>G MANE Select NP_055040.2:n.504-59T>G
NM_001363656.2:c.-34-59T>G NP_001350585.1:n.-34-59T>G
NR_033500.2:n.448-59T>G