Canonical Allele Identifier: CA407178775
Gene: PPP2R1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.52190204A>T , CM000681.2:g.52190204A>T GRCh38
NC_000019.9:g.52693457A>T , CM000681.1:g.52693457A>T GRCh37
NC_000019.8:g.57385269A>T NCBI36
NG_047068.1:g.5403A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000454220.7:c.108A>T ENSP00000391905.3:p.Arg36Ser
ENST00000703395.1:c.-459-11740A>T ENSP00000515286.1:n.-459-11740A>T
ENST00000703396.1:n.123+30A>T
ENST00000703397.1:c.-657+30A>T ENSP00000515287.1:n.-657+30A>T
ENST00000703398.1:c.78+30A>T ENSP00000515288.1:n.78+30A>T
ENST00000703421.1:n.231+1048A>T
ENST00000703422.1:c.78+30A>T ENSP00000515292.1:n.78+30A>T
ENST00000322088.11:c.78+30A>T MANE Select ENSP00000324804.6:n.78+30A>T
ENST00000322088.10:c.78+30A>T ENSP00000324804.6:n.78+30A>T
ENST00000454220.6:c.108A>T ENSP00000391905.2:p.Arg36Ser
ENST00000468280.5:n.61+30A>T
ENST00000477989.1:c.78+30A>T ENSP00000471298.1:n.78+30A>T
ENST00000490868.5:c.78+30A>T ENSP00000469150.1:n.78+30A>T
ENST00000628959.1:c.78+30A>T ENSP00000485914.1:n.78+30A>T
NM_014225.5:c.78+30A>T NP_055040.2:n.78+30A>T
NR_033500.1:n.373+30A>T
NM_014225.6:c.78+30A>T MANE Select NP_055040.2:n.78+30A>T
NR_033500.2:n.123+30A>T