Canonical Allele Identifier: CA9621281

Gene: PPP2R1A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52205951T>C , CM000681.2:g.52205951T>C	GRCh38
NC_000019.9:g.52709204T>C , CM000681.1:g.52709204T>C	GRCh37
NC_000019.8:g.57401016T>C	NCBI36
NG_047068.1:g.21150T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454220.7:c.290-12T>C	ENSP00000391905.3:n.290-12T>C
ENST00000703395.1:c.-368-12T>C	ENSP00000515286.1:n.-368-12T>C
ENST00000703396.1:n.214+3917T>C
ENST00000703397.1:c.-368-12T>C	ENSP00000515287.1:n.-368-12T>C
ENST00000703398.1:c.200T>C	ENSP00000515288.1:p.Leu67Pro
ENST00000703399.1:n.548-12T>C
ENST00000703400.1:n.414-12T>C
ENST00000703421.1:n.323-12T>C
ENST00000703422.1:c.146-12T>C	ENSP00000515292.1:n.146-12T>C
ENST00000703423.1:c.-368-12T>C	ENSP00000515293.1:n.-368-12T>C
ENST00000322088.11:c.170-12T>C MANE Select	ENSP00000324804.6:n.170-12T>C
ENST00000322088.10:c.170-12T>C	ENSP00000324804.6:n.170-12T>C
ENST00000454220.6:c.290-12T>C	ENSP00000391905.2:n.290-12T>C
ENST00000462990.5:c.-368-12T>C	ENSP00000470504.1:n.-368-12T>C
ENST00000468280.5:n.153-12T>C
ENST00000473455.2:n.269-12T>C
ENST00000490868.5:c.*178-12T>C	ENSP00000469150.1:n.*178-12T>C
ENST00000495876.5:n.425-12T>C
NM_014225.5:c.170-12T>C	NP_055040.2:n.170-12T>C
NR_033500.1:n.464+3917T>C
NM_001363656.1:c.-368-12T>C	NP_001350585.1:n.-368-12T>C
NM_014225.6:c.170-12T>C MANE Select	NP_055040.2:n.170-12T>C
NM_001363656.2:c.-368-12T>C	NP_001350585.1:n.-368-12T>C
NR_033500.2:n.214+3917T>C