Canonical Allele Identifier: CA891840836

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933066_87933067delinsGT , CM000672.2:g.87933066_87933067delinsGT	GRCh38
NC_000010.10:g.89692823_89692824delinsGT , CM000672.1:g.89692823_89692824delinsGT	GRCh37
NC_000010.9:g.89682803_89682804delinsGT	NCBI36
NG_007466.2:g.74628_74629delinsGT , LRG_311:g.74628_74629delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.307_308delinsGT	ENSP00000514759.2:p.Pro103Val
ENST00000710265.1:c.307_308delinsGT	ENSP00000518161.1:p.Pro103Val
ENST00000472832.3:c.307_308delinsGT	ENSP00000483066.2:p.Pro103Val
ENST00000688158.2:n.1042_1043delinsGT
ENST00000688922.2:c.*137_*138delinsGT	ENSP00000508742.2:n.*137_*138delinsGT
ENST00000700021.1:c.262_263delinsGT	ENSP00000514757.1:p.Pro88Val
ENST00000700022.1:c.307_308delinsGT	ENSP00000514758.1:p.Pro103Val
ENST00000700029.1:c.141_142delinsGT
ENST00000706954.1:c.307_308delinsGT	ENSP00000516674.1:p.Pro103Val
ENST00000706955.1:c.*342_*343delinsGT	ENSP00000516675.1:n.*342_*343delinsGT
ENST00000686459.1:c.307_308delinsGT	ENSP00000508909.1:p.Pro103Val
ENST00000688158.1:c.*418_*419delinsGT	ENSP00000509254.1:n.*418_*419delinsGT
ENST00000688308.1:c.307_308delinsGT	ENSP00000508752.1:p.Pro103Val
ENST00000688922.1:c.228_229delinsGT
ENST00000693560.1:c.826_827delinsGT	ENSP00000509861.1:p.Pro276Val
ENST00000371953.8:c.307_308delinsGT MANE Select	ENSP00000361021.3:p.Pro103Val
ENST00000371953.7:c.307_308delinsGT	ENSP00000361021.3:p.Pro103Val
ENST00000498703.1:n.133_134delinsGT
ENST00000610634.1:c.205_206delinsGT	ENSP00000477517.1:p.Pro69Val
NM_000314.5:c.307_308delinsGT	NP_000305.3:p.Pro103Val
NM_000314.6:c.307_308delinsGT	NP_000305.3:p.Pro103Val
NM_001304717.2:c.826_827delinsGT	NP_001291646.2:p.Pro276Val
NM_001304718.1:c.-444_-443delinsGT	NP_001291647.1:n.-444_-443delinsGT
XM_006717926.2:c.262_263delinsGT	XP_006717989.1:p.Pro88Val
XM_011539981.1:c.307_308delinsGT	XP_011538283.1:p.Pro103Val
XM_011539982.1:c.211_212delinsGT	XP_011538284.1:p.Pro71Val
XR_945789.1:n.1019_1020delinsGT
XR_945790.1:n.1019_1020delinsGT
XR_945791.1:n.1019_1020delinsGT
NM_000314.7:c.307_308delinsGT	NP_000305.3:p.Pro103Val
NM_001304717.5:c.826_827delinsGT	NP_001291646.4:p.Pro276Val
NM_001304718.2:c.-444_-443delinsGT	NP_001291647.1:n.-444_-443delinsGT
NM_000314.8:c.307_308delinsGT MANE Select	NP_000305.3:p.Pro103Val