Canonical Allele Identifier: CA2586787396
Gene: PPP2R1A HGNC NCBI

Linked Data

dbSNP Id: rs2122333838

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.52212654G>C , CM000681.2:g.52212654G>C GRCh38
NC_000019.9:g.52715907G>C , CM000681.1:g.52715907G>C GRCh37
NC_000019.8:g.57407719G>C NCBI36
NG_047068.1:g.27853G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000454220.7:c.624-32G>C ENSP00000391905.3:n.624-32G>C
ENST00000703395.1:c.-34-32G>C ENSP00000515286.1:n.-34-32G>C
ENST00000703396.1:n.448-32G>C
ENST00000703397.1:c.-34-32G>C ENSP00000515287.1:n.-34-32G>C
ENST00000703398.1:c.546-32G>C ENSP00000515288.1:n.546-32G>C
ENST00000703421.1:n.657-32G>C
ENST00000703422.1:c.480-32G>C ENSP00000515292.1:n.480-32G>C
ENST00000703423.1:c.-34-32G>C ENSP00000515293.1:n.-34-32G>C
ENST00000322088.11:c.504-32G>C MANE Select ENSP00000324804.6:n.504-32G>C
ENST00000322088.10:c.504-32G>C ENSP00000324804.6:n.504-32G>C
ENST00000454220.6:c.624-32G>C ENSP00000391905.2:n.624-32G>C
ENST00000462047.1:n.163G>C
ENST00000462990.5:c.-34-32G>C ENSP00000470504.1:n.-34-32G>C
ENST00000473455.2:n.603-32G>C
NM_014225.5:c.504-32G>C NP_055040.2:n.504-32G>C
NR_033500.1:n.698-32G>C
NM_001363656.1:c.-34-32G>C NP_001350585.1:n.-34-32G>C
NM_014225.6:c.504-32G>C MANE Select NP_055040.2:n.504-32G>C
NM_001363656.2:c.-34-32G>C NP_001350585.1:n.-34-32G>C
NR_033500.2:n.448-32G>C