Canonical Allele Identifier: CA3015299883

Gene: PPP2R2B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.146878733_146878734insACTGCT , CM000667.2:g.146878733_146878734insACTGCT	GRCh38
NC_000005.9:g.146258296_146258297insACTGCT , CM000667.1:g.146258296_146258297insACTGCT	GRCh37
NC_000005.8:g.146238489_146238490insACTGCT	NCBI36
NG_011570.1:g.207742_207743insTAGCAG
NG_011570.2:g.207742_207743insTAGCAG

Transcript Alleles

HGVS	Amino-acid Change
NM_181675.4:c.-263_-262insTAGCAG MANE Select	NP_858061.3:n.-263_-262insTAGCAG
ENST00000394411.9:c.-263_-262insTAGCAG MANE Select	ENSP00000377933.3:n.-263_-262insTAGCAG
NM_001271899.1:c.89-177587_89-177586insTAGCAG	NP_001258828.1:n.89-177587_89-177586insTAGCAG
NM_001271900.1:c.51-534_51-533insTAGCAG	NP_001258829.1:n.51-534_51-533insTAGCAG
NM_001271900.2:c.51-534_51-533insTAGCAG	NP_001258829.1:n.51-534_51-533insTAGCAG
NM_001271948.1:c.-776_-775insTAGCAG	NP_001258877.1:n.-776_-775insTAGCAG
NM_001271948.2:c.-776_-775insTAGCAG	NP_001258877.1:n.-776_-775insTAGCAG
NM_181674.2:c.75-534_75-533insTAGCAG	NP_858060.2:n.75-534_75-533insTAGCAG
NM_181674.3:c.75-534_75-533insTAGCAG	NP_858060.2:n.75-534_75-533insTAGCAG
NM_181675.3:c.56_57insTAGCAG	NP_858061.2:p.Ser19_Cys20insSerSer
NM_181676.2:c.79+176936_79+176937insTAGCAG	NP_858062.1:n.79+176936_79+176937insTAGCAG
NM_181676.3:c.79+176936_79+176937insTAGCAG	NP_858062.1:n.79+176936_79+176937insTAGCAG
NM_181677.2:c.10+156440_10+156441insTAGCAG	NP_858063.1:n.10+156440_10+156441insTAGCAG
NM_181678.2:c.-48-22146_-48-22145insTAGCAG	NP_858064.1:n.-48-22146_-48-22145insTAGCAG
NR_073526.1:n.57_58insTAGCAG
NR_073526.2:n.29_30insTAGCAG
NR_073527.1:n.199_200insTAGCAG
NR_073527.2:n.29_30insTAGCAG
ENST00000336640.10:c.79+176936_79+176937insTAGCAG	ENSP00000336591.6:n.79+176936_79+176937insTAGCAG
ENST00000394411.8:c.-263_-262insTAGCAG	ENSP00000377933.3:n.-263_-262insTAGCAG
ENST00000394413.7:c.51-534_51-533insTAGCAG	ENSP00000377935.4:n.51-534_51-533insTAGCAG
ENST00000394414.5:c.75-534_75-533insTAGCAG	ENSP00000377936.1:n.75-534_75-533insTAGCAG
ENST00000453001.5:c.-776_-775insTAGCAG	ENSP00000398779.2:n.-776_-775insTAGCAG
ENST00000502876.1:n.362+40955_362+40956insTAGCAG
ENST00000504198.5:c.89-177587_89-177586insTAGCAG	ENSP00000421396.1:n.89-177587_89-177586insTAGCAG
ENST00000504565.1:c.11-534_11-533insTAGCAG	ENSP00000425413.1:n.11-534_11-533insTAGCAG
ENST00000508267.5:c.10+156440_10+156441insTAGCAG	ENSP00000421224.1:n.10+156440_10+156441insTAGCAG
ENST00000508545.6:c.-48-22146_-48-22145insTAGCAG	ENSP00000431320.1:n.-48-22146_-48-22145insTAGCAG
ENST00000509721.1:n.281-534_281-533insTAGCAG
ENST00000512011.5:c.*18+161988_*18+161989insTAGCAG	ENSP00000424409.1:n.*18+161988_*18+161989insTAGCAG
ENST00000515880.5:c.*27+175869_*27+175870insTAGCAG	ENSP00000421577.1:n.*27+175869_*27+175870insTAGCAG
ENST00000520231.1:n.198+43596_198+43597insTAGCAG
ENST00000522831.1:n.268-22146_268-22145insTAGCAG
ENST00000528601.5:c.-125+403_-125+404insTAGCAG	ENSP00000433890.1:n.-125+403_-125+404insTAGCAG
ENST00000530902.5:n.166_167insTAGCAG
ENST00000532154.5:c.-153_-152insTAGCAG	ENSP00000434497.1:n.-153_-152insTAGCAG