Canonical Allele Identifier: CA891835054

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960949_87960950delinsTG , CM000672.2:g.87960949_87960950delinsTG	GRCh38
NC_000010.10:g.89720706_89720707delinsTG , CM000672.1:g.89720706_89720707delinsTG	GRCh37
NC_000010.9:g.89710686_89710687delinsTG	NCBI36
NG_007466.2:g.102511_102512delinsTG , LRG_311:g.102511_102512delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.950_951delinsTG	ENSP00000514759.2:p.Thr317Met
ENST00000710265.1:c.857_858delinsTG	ENSP00000518161.1:p.Thr286Met
ENST00000472832.3:c.857_858delinsTG	ENSP00000483066.2:p.Thr286Met
ENST00000688158.2:n.1592_1593delinsTG
ENST00000688922.2:c.*687_*688delinsTG	ENSP00000508742.2:n.*687_*688delinsTG
ENST00000700021.1:c.812_813delinsTG	ENSP00000514757.1:p.Thr271Met
ENST00000700022.1:c.*196_*197delinsTG	ENSP00000514758.1:n.*196_*197delinsTG
ENST00000700023.1:n.2015_2016delinsTG
ENST00000700024.1:n.2249_2250delinsTG
ENST00000700025.1:n.1626_1627delinsTG
ENST00000700026.1:n.494_495delinsTG
ENST00000700029.1:c.784_785delinsTG
ENST00000706954.1:c.857_858delinsTG	ENSP00000516674.1:p.Thr286Met
ENST00000706955.1:c.*892_*893delinsTG	ENSP00000516675.1:n.*892_*893delinsTG
ENST00000686459.1:c.*443_*444delinsTG	ENSP00000508909.1:n.*443_*444delinsTG
ENST00000688158.1:c.*968_*969delinsTG	ENSP00000509254.1:n.*968_*969delinsTG
ENST00000688308.1:c.857_858delinsTG	ENSP00000508752.1:p.Thr286Met
ENST00000688922.1:c.778_779delinsTG
ENST00000693560.1:c.1376_1377delinsTG	ENSP00000509861.1:p.Thr459Met
ENST00000371953.8:c.857_858delinsTG MANE Select	ENSP00000361021.3:p.Thr286Met
ENST00000371953.7:c.857_858delinsTG	ENSP00000361021.3:p.Thr286Met
ENST00000472832.2:c.284_285delinsTG	ENSP00000483066.1:p.Thr95Met
NM_000314.5:c.857_858delinsTG	NP_000305.3:p.Thr286Met
NM_000314.6:c.857_858delinsTG	NP_000305.3:p.Thr286Met
NM_001304717.2:c.1376_1377delinsTG	NP_001291646.2:p.Thr459Met
NM_001304718.1:c.266_267delinsTG	NP_001291647.1:p.Thr89Met
XM_006717926.2:c.812_813delinsTG	XP_006717989.1:p.Thr271Met
XM_011539981.1:c.857_858delinsTG	XP_011538283.1:p.Thr286Met
XM_011539982.1:c.761_762delinsTG	XP_011538284.1:p.Thr254Met
XR_945791.1:n.1427_1428delinsTG
NM_000314.7:c.857_858delinsTG	NP_000305.3:p.Thr286Met
NM_001304717.5:c.1376_1377delinsTG	NP_001291646.4:p.Thr459Met
NM_001304718.2:c.266_267delinsTG	NP_001291647.1:p.Thr89Met
NM_000314.8:c.857_858delinsTG MANE Select	NP_000305.3:p.Thr286Met