Canonical Allele Identifier: CA3062659611

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933154_87933177del , CM000672.2:g.87933154_87933177del	GRCh38
NC_000010.10:g.89692911_89692934del , CM000672.1:g.89692911_89692934del	GRCh37
NC_000010.9:g.89682891_89682914del	NCBI36
NG_007466.2:g.74716_74739del , LRG_311:g.74716_74739del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.395_418del	ENSP00000514759.2:p.Gly132_Leu140delinsVal
ENST00000710265.1:c.395_418del	ENSP00000518161.1:p.Gly132_Leu140delinsVal
ENST00000472832.3:c.395_418del	ENSP00000483066.2:p.Gly132_Leu140delinsVal
ENST00000688158.2:n.1130_1153del
ENST00000688922.2:c.*225_*248del	ENSP00000508742.2:n.*225_*248del
ENST00000700021.1:c.350_373del	ENSP00000514757.1:p.Gly117_Leu125delinsVal
ENST00000700022.1:c.395_418del	ENSP00000514758.1:p.Gly132_Leu140delinsVal
ENST00000700029.1:c.229_252del
ENST00000706954.1:c.395_418del	ENSP00000516674.1:p.Gly132_Leu140delinsVal
ENST00000706955.1:c.*430_*453del	ENSP00000516675.1:n.*430_*453del
ENST00000686459.1:c.395_418del	ENSP00000508909.1:p.Gly132_Leu140delinsVal
ENST00000688158.1:c.*506_*529del	ENSP00000509254.1:n.*506_*529del
ENST00000688308.1:c.395_418del	ENSP00000508752.1:p.Gly132_Leu140delinsVal
ENST00000688922.1:c.316_339del
ENST00000693560.1:c.914_937del	ENSP00000509861.1:p.Gly305_Leu313delinsVal
ENST00000371953.8:c.395_418del MANE Select	ENSP00000361021.3:p.Gly132_Leu140delinsVal
ENST00000371953.7:c.395_418del	ENSP00000361021.3:p.Gly132_Leu140delinsVal
ENST00000498703.1:n.221_244del
ENST00000610634.1:c.293_316del	ENSP00000477517.1:p.Gly98_Leu106delinsVal
NM_000314.5:c.395_418del	NP_000305.3:p.Gly132_Leu140delinsVal
NM_000314.6:c.395_418del	NP_000305.3:p.Gly132_Leu140delinsVal
NM_001304717.2:c.914_937del	NP_001291646.2:p.Gly305_Leu313delinsVal
NM_001304718.1:c.-356_-333del	NP_001291647.1:n.-356_-333del
XM_006717926.2:c.350_373del	XP_006717989.1:p.Gly117_Leu125delinsVal
XM_011539981.1:c.395_418del	XP_011538283.1:p.Gly132_Leu140delinsVal
XM_011539982.1:c.299_322del	XP_011538284.1:p.Gly100_Leu108delinsVal
XR_945789.1:n.1107_1130del
XR_945790.1:n.1107_1130del
XR_945791.1:n.1107_1130del
NM_000314.7:c.395_418del	NP_000305.3:p.Gly132_Leu140delinsVal
NM_001304717.5:c.914_937del	NP_001291646.4:p.Gly305_Leu313delinsVal
NM_001304718.2:c.-356_-333del	NP_001291647.1:n.-356_-333del
NM_000314.8:c.395_418del MANE Select	NP_000305.3:p.Gly132_Leu140delinsVal