Canonical Allele Identifier: CA891835046

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960948_87960950delinsTTG , CM000672.2:g.87960948_87960950delinsTTG	GRCh38
NC_000010.10:g.89720705_89720707delinsTTG , CM000672.1:g.89720705_89720707delinsTTG	GRCh37
NC_000010.9:g.89710685_89710687delinsTTG	NCBI36
NG_007466.2:g.102510_102512delinsTTG , LRG_311:g.102510_102512delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.949_951delinsTTG	ENSP00000514759.2:p.Thr317Leu
ENST00000710265.1:c.856_858delinsTTG	ENSP00000518161.1:p.Thr286Leu
ENST00000472832.3:c.856_858delinsTTG	ENSP00000483066.2:p.Thr286Leu
ENST00000688158.2:n.1591_1593delinsTTG
ENST00000688922.2:c.*686_*688delinsTTG	ENSP00000508742.2:n.*686_*688delinsTTG
ENST00000700021.1:c.811_813delinsTTG	ENSP00000514757.1:p.Thr271Leu
ENST00000700022.1:c.*195_*197delinsTTG	ENSP00000514758.1:n.*195_*197delinsTTG
ENST00000700023.1:n.2014_2016delinsTTG
ENST00000700024.1:n.2248_2250delinsTTG
ENST00000700025.1:n.1625_1627delinsTTG
ENST00000700026.1:n.493_495delinsTTG
ENST00000700029.1:c.783_785delinsTTG
ENST00000706954.1:c.856_858delinsTTG	ENSP00000516674.1:p.Thr286Leu
ENST00000706955.1:c.*891_*893delinsTTG	ENSP00000516675.1:n.*891_*893delinsTTG
ENST00000686459.1:c.*442_*444delinsTTG	ENSP00000508909.1:n.*442_*444delinsTTG
ENST00000688158.1:c.*967_*969delinsTTG	ENSP00000509254.1:n.*967_*969delinsTTG
ENST00000688308.1:c.856_858delinsTTG	ENSP00000508752.1:p.Thr286Leu
ENST00000688922.1:c.777_779delinsTTG
ENST00000693560.1:c.1375_1377delinsTTG	ENSP00000509861.1:p.Thr459Leu
ENST00000371953.8:c.856_858delinsTTG MANE Select	ENSP00000361021.3:p.Thr286Leu
ENST00000371953.7:c.856_858delinsTTG	ENSP00000361021.3:p.Thr286Leu
ENST00000472832.2:c.283_285delinsTTG	ENSP00000483066.1:p.Thr95Leu
NM_000314.5:c.856_858delinsTTG	NP_000305.3:p.Thr286Leu
NM_000314.6:c.856_858delinsTTG	NP_000305.3:p.Thr286Leu
NM_001304717.2:c.1375_1377delinsTTG	NP_001291646.2:p.Thr459Leu
NM_001304718.1:c.265_267delinsTTG	NP_001291647.1:p.Thr89Leu
XM_006717926.2:c.811_813delinsTTG	XP_006717989.1:p.Thr271Leu
XM_011539981.1:c.856_858delinsTTG	XP_011538283.1:p.Thr286Leu
XM_011539982.1:c.760_762delinsTTG	XP_011538284.1:p.Thr254Leu
XR_945791.1:n.1426_1428delinsTTG
NM_000314.7:c.856_858delinsTTG	NP_000305.3:p.Thr286Leu
NM_001304717.5:c.1375_1377delinsTTG	NP_001291646.4:p.Thr459Leu
NM_001304718.2:c.265_267delinsTTG	NP_001291647.1:p.Thr89Leu
NM_000314.8:c.856_858delinsTTG MANE Select	NP_000305.3:p.Thr286Leu