Canonical Allele Identifier: CA891834726

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960928_87960929delinsCT , CM000672.2:g.87960928_87960929delinsCT	GRCh38
NC_000010.10:g.89720685_89720686delinsCT , CM000672.1:g.89720685_89720686delinsCT	GRCh37
NC_000010.9:g.89710665_89710666delinsCT	NCBI36
NG_007466.2:g.102490_102491delinsCT , LRG_311:g.102490_102491delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.929_930delinsCT	ENSP00000514759.2:p.Phe310Ser
ENST00000710265.1:c.836_837delinsCT	ENSP00000518161.1:p.Phe279Ser
ENST00000472832.3:c.836_837delinsCT	ENSP00000483066.2:p.Phe279Ser
ENST00000688158.2:n.1571_1572delinsCT
ENST00000688922.2:c.*666_*667delinsCT	ENSP00000508742.2:n.*666_*667delinsCT
ENST00000700021.1:c.791_792delinsCT	ENSP00000514757.1:p.Phe264Ser
ENST00000700022.1:c.*175_*176delinsCT	ENSP00000514758.1:n.*175_*176delinsCT
ENST00000700023.1:n.1994_1995delinsCT
ENST00000700024.1:n.2228_2229delinsCT
ENST00000700025.1:n.1605_1606delinsCT
ENST00000700026.1:n.473_474delinsCT
ENST00000700029.1:c.763_764delinsCT
ENST00000706954.1:c.836_837delinsCT	ENSP00000516674.1:p.Phe279Ser
ENST00000706955.1:c.*871_*872delinsCT	ENSP00000516675.1:n.*871_*872delinsCT
ENST00000686459.1:c.*422_*423delinsCT	ENSP00000508909.1:n.*422_*423delinsCT
ENST00000688158.1:c.*947_*948delinsCT	ENSP00000509254.1:n.*947_*948delinsCT
ENST00000688308.1:c.836_837delinsCT	ENSP00000508752.1:p.Phe279Ser
ENST00000688922.1:c.757_758delinsCT
ENST00000693560.1:c.1355_1356delinsCT	ENSP00000509861.1:p.Phe452Ser
ENST00000371953.8:c.836_837delinsCT MANE Select	ENSP00000361021.3:p.Phe279Ser
ENST00000371953.7:c.836_837delinsCT	ENSP00000361021.3:p.Phe279Ser
ENST00000472832.2:c.263_264delinsCT	ENSP00000483066.1:p.Phe88Ser
NM_000314.5:c.836_837delinsCT	NP_000305.3:p.Phe279Ser
NM_000314.6:c.836_837delinsCT	NP_000305.3:p.Phe279Ser
NM_001304717.2:c.1355_1356delinsCT	NP_001291646.2:p.Phe452Ser
NM_001304718.1:c.245_246delinsCT	NP_001291647.1:p.Phe82Ser
XM_006717926.2:c.791_792delinsCT	XP_006717989.1:p.Phe264Ser
XM_011539981.1:c.836_837delinsCT	XP_011538283.1:p.Phe279Ser
XM_011539982.1:c.740_741delinsCT	XP_011538284.1:p.Phe247Ser
XR_945791.1:n.1406_1407delinsCT
NM_000314.7:c.836_837delinsCT	NP_000305.3:p.Phe279Ser
NM_001304717.5:c.1355_1356delinsCT	NP_001291646.4:p.Phe452Ser
NM_001304718.2:c.245_246delinsCT	NP_001291647.1:p.Phe82Ser
NM_000314.8:c.836_837delinsCT MANE Select	NP_000305.3:p.Phe279Ser