Canonical Allele Identifier: CA891841276

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961038_87961039delinsAC , CM000672.2:g.87961038_87961039delinsAC	GRCh38
NC_000010.10:g.89720795_89720796delinsAC , CM000672.1:g.89720795_89720796delinsAC	GRCh37
NC_000010.9:g.89710775_89710776delinsAC	NCBI36
NG_007466.2:g.102600_102601delinsAC , LRG_311:g.102600_102601delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1039_1040delinsAC	ENSP00000514759.2:p.Leu347Thr
ENST00000710265.1:c.946_947delinsAC	ENSP00000518161.1:p.Leu316Thr
ENST00000472832.3:c.946_947delinsAC	ENSP00000483066.2:p.Leu316Thr
ENST00000688158.2:n.1681_1682delinsAC
ENST00000688922.2:c.*776_*777delinsAC	ENSP00000508742.2:n.*776_*777delinsAC
ENST00000700021.1:c.901_902delinsAC	ENSP00000514757.1:p.Leu301Thr
ENST00000700022.1:c.*285_*286delinsAC	ENSP00000514758.1:n.*285_*286delinsAC
ENST00000700023.1:n.2104_2105delinsAC
ENST00000700024.1:n.2338_2339delinsAC
ENST00000700025.1:n.1715_1716delinsAC
ENST00000700026.1:n.583_584delinsAC
ENST00000706954.1:c.946_947delinsAC	ENSP00000516674.1:p.Leu316Thr
ENST00000706955.1:c.*981_*982delinsAC	ENSP00000516675.1:n.*981_*982delinsAC
ENST00000686459.1:c.*532_*533delinsAC	ENSP00000508909.1:n.*532_*533delinsAC
ENST00000688158.1:c.*1057_*1058delinsAC	ENSP00000509254.1:n.*1057_*1058delinsAC
ENST00000688308.1:c.946_947delinsAC	ENSP00000508752.1:p.Leu316Thr
ENST00000688922.1:c.867_868delinsAC
ENST00000693560.1:c.1465_1466delinsAC	ENSP00000509861.1:p.Leu489Thr
ENST00000371953.8:c.946_947delinsAC MANE Select	ENSP00000361021.3:p.Leu316Thr
ENST00000371953.7:c.946_947delinsAC	ENSP00000361021.3:p.Leu316Thr
ENST00000472832.2:c.373_374delinsAC	ENSP00000483066.1:p.Leu125Thr
NM_000314.5:c.946_947delinsAC	NP_000305.3:p.Leu316Thr
NM_000314.6:c.946_947delinsAC	NP_000305.3:p.Leu316Thr
NM_001304717.2:c.1465_1466delinsAC	NP_001291646.2:p.Leu489Thr
NM_001304718.1:c.355_356delinsAC	NP_001291647.1:p.Leu119Thr
XM_006717926.2:c.901_902delinsAC	XP_006717989.1:p.Leu301Thr
XM_011539981.1:c.946_947delinsAC	XP_011538283.1:p.Leu316Thr
XM_011539982.1:c.850_851delinsAC	XP_011538284.1:p.Leu284Thr
XR_945791.1:n.1516_1517delinsAC
NM_000314.7:c.946_947delinsAC	NP_000305.3:p.Leu316Thr
NM_001304717.5:c.1465_1466delinsAC	NP_001291646.4:p.Leu489Thr
NM_001304718.2:c.355_356delinsAC	NP_001291647.1:p.Leu119Thr
NM_000314.8:c.946_947delinsAC MANE Select	NP_000305.3:p.Leu316Thr