Canonical Allele Identifier: CA2341728215
Gene: PPP2R1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.52190192_52190193delinsGA , CM000681.2:g.52190192_52190193delinsGA GRCh38
NC_000019.9:g.52693445_52693446delinsGA , CM000681.1:g.52693445_52693446delinsGA GRCh37
NC_000019.8:g.57385257_57385258delinsGA NCBI36
NG_047068.1:g.5391_5392delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000454220.7:c.96_97delinsGA ENSP00000391905.3:p.Gly32=
ENST00000703395.1:c.-459-11752_-459-11751delinsGA ENSP00000515286.1:n.-459-11752_-459-11751delinsGA
ENST00000703396.1:n.123+18_123+19delinsGA
ENST00000703397.1:c.-657+18_-657+19delinsGA ENSP00000515287.1:n.-657+18_-657+19delinsGA
ENST00000703398.1:c.78+18_78+19delinsGA ENSP00000515288.1:n.78+18_78+19delinsGA
ENST00000703421.1:n.231+1036_231+1037delinsGA
ENST00000703422.1:c.78+18_78+19delinsGA ENSP00000515292.1:n.78+18_78+19delinsGA
ENST00000322088.11:c.78+18_78+19delinsGA MANE Select ENSP00000324804.6:n.78+18_78+19delinsGA
ENST00000322088.10:c.78+18_78+19delinsGA ENSP00000324804.6:n.78+18_78+19delinsGA
ENST00000454220.6:c.96_97delinsGA ENSP00000391905.2:p.Gly32=
ENST00000468280.5:n.61+18_61+19delinsGA
ENST00000477989.1:c.78+18_78+19delinsGA ENSP00000471298.1:n.78+18_78+19delinsGA
ENST00000490868.5:c.78+18_78+19delinsGA ENSP00000469150.1:n.78+18_78+19delinsGA
ENST00000628959.1:c.78+18_78+19delinsGA ENSP00000485914.1:n.78+18_78+19delinsGA
NM_014225.5:c.78+18_78+19delinsGA NP_055040.2:n.78+18_78+19delinsGA
NR_033500.1:n.373+18_373+19delinsGA
NM_014225.6:c.78+18_78+19delinsGA MANE Select NP_055040.2:n.78+18_78+19delinsGA
NR_033500.2:n.123+18_123+19delinsGA