Canonical Allele Identifier: CA891835042

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960948_87960950delinsTAT , CM000672.2:g.87960948_87960950delinsTAT	GRCh38
NC_000010.10:g.89720705_89720707delinsTAT , CM000672.1:g.89720705_89720707delinsTAT	GRCh37
NC_000010.9:g.89710685_89710687delinsTAT	NCBI36
NG_007466.2:g.102510_102512delinsTAT , LRG_311:g.102510_102512delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.949_951delinsTAT	ENSP00000514759.2:p.Thr317Tyr
ENST00000710265.1:c.856_858delinsTAT	ENSP00000518161.1:p.Thr286Tyr
ENST00000472832.3:c.856_858delinsTAT	ENSP00000483066.2:p.Thr286Tyr
ENST00000688158.2:n.1591_1593delinsTAT
ENST00000688922.2:c.*686_*688delinsTAT	ENSP00000508742.2:n.*686_*688delinsTAT
ENST00000700021.1:c.811_813delinsTAT	ENSP00000514757.1:p.Thr271Tyr
ENST00000700022.1:c.*195_*197delinsTAT	ENSP00000514758.1:n.*195_*197delinsTAT
ENST00000700023.1:n.2014_2016delinsTAT
ENST00000700024.1:n.2248_2250delinsTAT
ENST00000700025.1:n.1625_1627delinsTAT
ENST00000700026.1:n.493_495delinsTAT
ENST00000700029.1:c.783_785delinsTAT
ENST00000706954.1:c.856_858delinsTAT	ENSP00000516674.1:p.Thr286Tyr
ENST00000706955.1:c.*891_*893delinsTAT	ENSP00000516675.1:n.*891_*893delinsTAT
ENST00000686459.1:c.*442_*444delinsTAT	ENSP00000508909.1:n.*442_*444delinsTAT
ENST00000688158.1:c.*967_*969delinsTAT	ENSP00000509254.1:n.*967_*969delinsTAT
ENST00000688308.1:c.856_858delinsTAT	ENSP00000508752.1:p.Thr286Tyr
ENST00000688922.1:c.777_779delinsTAT
ENST00000693560.1:c.1375_1377delinsTAT	ENSP00000509861.1:p.Thr459Tyr
ENST00000371953.8:c.856_858delinsTAT MANE Select	ENSP00000361021.3:p.Thr286Tyr
ENST00000371953.7:c.856_858delinsTAT	ENSP00000361021.3:p.Thr286Tyr
ENST00000472832.2:c.283_285delinsTAT	ENSP00000483066.1:p.Thr95Tyr
NM_000314.5:c.856_858delinsTAT	NP_000305.3:p.Thr286Tyr
NM_000314.6:c.856_858delinsTAT	NP_000305.3:p.Thr286Tyr
NM_001304717.2:c.1375_1377delinsTAT	NP_001291646.2:p.Thr459Tyr
NM_001304718.1:c.265_267delinsTAT	NP_001291647.1:p.Thr89Tyr
XM_006717926.2:c.811_813delinsTAT	XP_006717989.1:p.Thr271Tyr
XM_011539981.1:c.856_858delinsTAT	XP_011538283.1:p.Thr286Tyr
XM_011539982.1:c.760_762delinsTAT	XP_011538284.1:p.Thr254Tyr
XR_945791.1:n.1426_1428delinsTAT
NM_000314.7:c.856_858delinsTAT	NP_000305.3:p.Thr286Tyr
NM_001304717.5:c.1375_1377delinsTAT	NP_001291646.4:p.Thr459Tyr
NM_001304718.2:c.265_267delinsTAT	NP_001291647.1:p.Thr89Tyr
NM_000314.8:c.856_858delinsTAT MANE Select	NP_000305.3:p.Thr286Tyr