Canonical Allele Identifier: CA2586787354
Gene: PPP2R1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.52212604G>T , CM000681.2:g.52212604G>T GRCh38
NC_000019.9:g.52715857G>T , CM000681.1:g.52715857G>T GRCh37
NC_000019.8:g.57407669G>T NCBI36
NG_047068.1:g.27803G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000454220.7:c.624-82G>T ENSP00000391905.3:n.624-82G>T
ENST00000703395.1:c.-34-82G>T ENSP00000515286.1:n.-34-82G>T
ENST00000703396.1:n.448-82G>T
ENST00000703397.1:c.-34-82G>T ENSP00000515287.1:n.-34-82G>T
ENST00000703398.1:c.546-82G>T ENSP00000515288.1:n.546-82G>T
ENST00000703421.1:n.657-82G>T
ENST00000703422.1:c.480-82G>T ENSP00000515292.1:n.480-82G>T
ENST00000703423.1:c.-34-82G>T ENSP00000515293.1:n.-34-82G>T
ENST00000322088.11:c.504-82G>T MANE Select ENSP00000324804.6:n.504-82G>T
ENST00000322088.10:c.504-82G>T ENSP00000324804.6:n.504-82G>T
ENST00000454220.6:c.624-82G>T ENSP00000391905.2:n.624-82G>T
ENST00000462047.1:n.113G>T
ENST00000462990.5:c.-34-82G>T ENSP00000470504.1:n.-34-82G>T
ENST00000473455.2:n.603-82G>T
NM_014225.5:c.504-82G>T NP_055040.2:n.504-82G>T
NR_033500.1:n.698-82G>T
NM_001363656.1:c.-34-82G>T NP_001350585.1:n.-34-82G>T
NM_014225.6:c.504-82G>T MANE Select NP_055040.2:n.504-82G>T
NM_001363656.2:c.-34-82G>T NP_001350585.1:n.-34-82G>T
NR_033500.2:n.448-82G>T