Canonical Allele Identifier: CA9621289

Gene: PPP2R1A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52206048C>T , CM000681.2:g.52206048C>T	GRCh38
NC_000019.9:g.52709301C>T , CM000681.1:g.52709301C>T	GRCh37
NC_000019.8:g.57401113C>T	NCBI36
NG_047068.1:g.21247C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454220.7:c.375C>T	ENSP00000391905.3:p.Tyr125=
ENST00000703395.1:c.-283C>T	ENSP00000515286.1:n.-283C>T
ENST00000703396.1:n.214+4014C>T
ENST00000703397.1:c.-283C>T	ENSP00000515287.1:n.-283C>T
ENST00000703398.1:c.297C>T	ENSP00000515288.1:p.Tyr99=
ENST00000703400.1:n.499C>T
ENST00000703421.1:n.408C>T
ENST00000703422.1:c.231C>T	ENSP00000515292.1:p.Tyr77=
ENST00000703423.1:c.-283C>T	ENSP00000515293.1:n.-283C>T
ENST00000322088.11:c.255C>T MANE Select	ENSP00000324804.6:p.Tyr85=
ENST00000322088.10:c.255C>T	ENSP00000324804.6:p.Tyr85=
ENST00000454220.6:c.375C>T	ENSP00000391905.2:p.Tyr125=
ENST00000462990.5:c.-283C>T	ENSP00000470504.1:n.-283C>T
ENST00000468280.5:n.238C>T
ENST00000473455.2:n.354C>T
ENST00000490868.5:c.*263C>T	ENSP00000469150.1:n.*263C>T
ENST00000495876.5:n.510C>T
NM_014225.5:c.255C>T	NP_055040.2:p.Tyr85=
NR_033500.1:n.464+4014C>T
NM_001363656.1:c.-283C>T	NP_001350585.1:n.-283C>T
NM_014225.6:c.255C>T MANE Select	NP_055040.2:p.Tyr85=
NM_001363656.2:c.-283C>T	NP_001350585.1:n.-283C>T
NR_033500.2:n.214+4014C>T