Canonical Allele Identifier: CA2735969979
Gene: PPP2R1A HGNC NCBI

Linked Data

dbSNP Id: rs2122333805

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.52212650G>A , CM000681.2:g.52212650G>A GRCh38
NC_000019.9:g.52715903G>A , CM000681.1:g.52715903G>A GRCh37
NC_000019.8:g.57407715G>A NCBI36
NG_047068.1:g.27849G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000454220.7:c.624-36G>A ENSP00000391905.3:n.624-36G>A
ENST00000703395.1:c.-34-36G>A ENSP00000515286.1:n.-34-36G>A
ENST00000703396.1:n.448-36G>A
ENST00000703397.1:c.-34-36G>A ENSP00000515287.1:n.-34-36G>A
ENST00000703398.1:c.546-36G>A ENSP00000515288.1:n.546-36G>A
ENST00000703421.1:n.657-36G>A
ENST00000703422.1:c.480-36G>A ENSP00000515292.1:n.480-36G>A
ENST00000703423.1:c.-34-36G>A ENSP00000515293.1:n.-34-36G>A
ENST00000322088.11:c.504-36G>A MANE Select ENSP00000324804.6:n.504-36G>A
ENST00000322088.10:c.504-36G>A ENSP00000324804.6:n.504-36G>A
ENST00000454220.6:c.624-36G>A ENSP00000391905.2:n.624-36G>A
ENST00000462047.1:n.159G>A
ENST00000462990.5:c.-34-36G>A ENSP00000470504.1:n.-34-36G>A
ENST00000473455.2:n.603-36G>A
NM_014225.5:c.504-36G>A NP_055040.2:n.504-36G>A
NR_033500.1:n.698-36G>A
NM_001363656.1:c.-34-36G>A NP_001350585.1:n.-34-36G>A
NM_014225.6:c.504-36G>A MANE Select NP_055040.2:n.504-36G>A
NM_001363656.2:c.-34-36G>A NP_001350585.1:n.-34-36G>A
NR_033500.2:n.448-36G>A