Canonical Allele Identifier: CA891835057

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960949_87960950delinsTT , CM000672.2:g.87960949_87960950delinsTT	GRCh38
NC_000010.10:g.89720706_89720707delinsTT , CM000672.1:g.89720706_89720707delinsTT	GRCh37
NC_000010.9:g.89710686_89710687delinsTT	NCBI36
NG_007466.2:g.102511_102512delinsTT , LRG_311:g.102511_102512delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.950_951delinsTT	ENSP00000514759.2:p.Thr317Ile
ENST00000710265.1:c.857_858delinsTT	ENSP00000518161.1:p.Thr286Ile
ENST00000472832.3:c.857_858delinsTT	ENSP00000483066.2:p.Thr286Ile
ENST00000688158.2:n.1592_1593delinsTT
ENST00000688922.2:c.*687_*688delinsTT	ENSP00000508742.2:n.*687_*688delinsTT
ENST00000700021.1:c.812_813delinsTT	ENSP00000514757.1:p.Thr271Ile
ENST00000700022.1:c.*196_*197delinsTT	ENSP00000514758.1:n.*196_*197delinsTT
ENST00000700023.1:n.2015_2016delinsTT
ENST00000700024.1:n.2249_2250delinsTT
ENST00000700025.1:n.1626_1627delinsTT
ENST00000700026.1:n.494_495delinsTT
ENST00000700029.1:c.784_785delinsTT
ENST00000706954.1:c.857_858delinsTT	ENSP00000516674.1:p.Thr286Ile
ENST00000706955.1:c.*892_*893delinsTT	ENSP00000516675.1:n.*892_*893delinsTT
ENST00000686459.1:c.*443_*444delinsTT	ENSP00000508909.1:n.*443_*444delinsTT
ENST00000688158.1:c.*968_*969delinsTT	ENSP00000509254.1:n.*968_*969delinsTT
ENST00000688308.1:c.857_858delinsTT	ENSP00000508752.1:p.Thr286Ile
ENST00000688922.1:c.778_779delinsTT
ENST00000693560.1:c.1376_1377delinsTT	ENSP00000509861.1:p.Thr459Ile
ENST00000371953.8:c.857_858delinsTT MANE Select	ENSP00000361021.3:p.Thr286Ile
ENST00000371953.7:c.857_858delinsTT	ENSP00000361021.3:p.Thr286Ile
ENST00000472832.2:c.284_285delinsTT	ENSP00000483066.1:p.Thr95Ile
NM_000314.5:c.857_858delinsTT	NP_000305.3:p.Thr286Ile
NM_000314.6:c.857_858delinsTT	NP_000305.3:p.Thr286Ile
NM_001304717.2:c.1376_1377delinsTT	NP_001291646.2:p.Thr459Ile
NM_001304718.1:c.266_267delinsTT	NP_001291647.1:p.Thr89Ile
XM_006717926.2:c.812_813delinsTT	XP_006717989.1:p.Thr271Ile
XM_011539981.1:c.857_858delinsTT	XP_011538283.1:p.Thr286Ile
XM_011539982.1:c.761_762delinsTT	XP_011538284.1:p.Thr254Ile
XR_945791.1:n.1427_1428delinsTT
NM_000314.7:c.857_858delinsTT	NP_000305.3:p.Thr286Ile
NM_001304717.5:c.1376_1377delinsTT	NP_001291646.4:p.Thr459Ile
NM_001304718.2:c.266_267delinsTT	NP_001291647.1:p.Thr89Ile
NM_000314.8:c.857_858delinsTT MANE Select	NP_000305.3:p.Thr286Ile