Canonical Allele Identifier: CA891835016

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960948_87960950delinsCAT , CM000672.2:g.87960948_87960950delinsCAT	GRCh38
NC_000010.10:g.89720705_89720707delinsCAT , CM000672.1:g.89720705_89720707delinsCAT	GRCh37
NC_000010.9:g.89710685_89710687delinsCAT	NCBI36
NG_007466.2:g.102510_102512delinsCAT , LRG_311:g.102510_102512delinsCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.949_951delinsCAT	ENSP00000514759.2:p.Thr317His
ENST00000710265.1:c.856_858delinsCAT	ENSP00000518161.1:p.Thr286His
ENST00000472832.3:c.856_858delinsCAT	ENSP00000483066.2:p.Thr286His
ENST00000688158.2:n.1591_1593delinsCAT
ENST00000688922.2:c.*686_*688delinsCAT	ENSP00000508742.2:n.*686_*688delinsCAT
ENST00000700021.1:c.811_813delinsCAT	ENSP00000514757.1:p.Thr271His
ENST00000700022.1:c.*195_*197delinsCAT	ENSP00000514758.1:n.*195_*197delinsCAT
ENST00000700023.1:n.2014_2016delinsCAT
ENST00000700024.1:n.2248_2250delinsCAT
ENST00000700025.1:n.1625_1627delinsCAT
ENST00000700026.1:n.493_495delinsCAT
ENST00000700029.1:c.783_785delinsCAT
ENST00000706954.1:c.856_858delinsCAT	ENSP00000516674.1:p.Thr286His
ENST00000706955.1:c.*891_*893delinsCAT	ENSP00000516675.1:n.*891_*893delinsCAT
ENST00000686459.1:c.*442_*444delinsCAT	ENSP00000508909.1:n.*442_*444delinsCAT
ENST00000688158.1:c.*967_*969delinsCAT	ENSP00000509254.1:n.*967_*969delinsCAT
ENST00000688308.1:c.856_858delinsCAT	ENSP00000508752.1:p.Thr286His
ENST00000688922.1:c.777_779delinsCAT
ENST00000693560.1:c.1375_1377delinsCAT	ENSP00000509861.1:p.Thr459His
ENST00000371953.8:c.856_858delinsCAT MANE Select	ENSP00000361021.3:p.Thr286His
ENST00000371953.7:c.856_858delinsCAT	ENSP00000361021.3:p.Thr286His
ENST00000472832.2:c.283_285delinsCAT	ENSP00000483066.1:p.Thr95His
NM_000314.5:c.856_858delinsCAT	NP_000305.3:p.Thr286His
NM_000314.6:c.856_858delinsCAT	NP_000305.3:p.Thr286His
NM_001304717.2:c.1375_1377delinsCAT	NP_001291646.2:p.Thr459His
NM_001304718.1:c.265_267delinsCAT	NP_001291647.1:p.Thr89His
XM_006717926.2:c.811_813delinsCAT	XP_006717989.1:p.Thr271His
XM_011539981.1:c.856_858delinsCAT	XP_011538283.1:p.Thr286His
XM_011539982.1:c.760_762delinsCAT	XP_011538284.1:p.Thr254His
XR_945791.1:n.1426_1428delinsCAT
NM_000314.7:c.856_858delinsCAT	NP_000305.3:p.Thr286His
NM_001304717.5:c.1375_1377delinsCAT	NP_001291646.4:p.Thr459His
NM_001304718.2:c.265_267delinsCAT	NP_001291647.1:p.Thr89His
NM_000314.8:c.856_858delinsCAT MANE Select	NP_000305.3:p.Thr286His