Canonical Allele Identifier: CA891836447

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961038_87961040delinsATT , CM000672.2:g.87961038_87961040delinsATT	GRCh38
NC_000010.10:g.89720795_89720797delinsATT , CM000672.1:g.89720795_89720797delinsATT	GRCh37
NC_000010.9:g.89710775_89710777delinsATT	NCBI36
NG_007466.2:g.102600_102602delinsATT , LRG_311:g.102600_102602delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1039_1041delinsATT	ENSP00000514759.2:p.Leu347Ile
ENST00000710265.1:c.946_948delinsATT	ENSP00000518161.1:p.Leu316Ile
ENST00000472832.3:c.946_948delinsATT	ENSP00000483066.2:p.Leu316Ile
ENST00000688158.2:n.1681_1683delinsATT
ENST00000688922.2:c.*776_*778delinsATT	ENSP00000508742.2:n.*776_*778delinsATT
ENST00000700021.1:c.901_903delinsATT	ENSP00000514757.1:p.Leu301Ile
ENST00000700022.1:c.*285_*287delinsATT	ENSP00000514758.1:n.*285_*287delinsATT
ENST00000700023.1:n.2104_2106delinsATT
ENST00000700024.1:n.2338_2340delinsATT
ENST00000700025.1:n.1715_1717delinsATT
ENST00000700026.1:n.583_585delinsATT
ENST00000706954.1:c.946_948delinsATT	ENSP00000516674.1:p.Leu316Ile
ENST00000706955.1:c.*981_*983delinsATT	ENSP00000516675.1:n.*981_*983delinsATT
ENST00000686459.1:c.*532_*534delinsATT	ENSP00000508909.1:n.*532_*534delinsATT
ENST00000688158.1:c.*1057_*1059delinsATT	ENSP00000509254.1:n.*1057_*1059delinsATT
ENST00000688308.1:c.946_948delinsATT	ENSP00000508752.1:p.Leu316Ile
ENST00000688922.1:c.867_869delinsATT
ENST00000693560.1:c.1465_1467delinsATT	ENSP00000509861.1:p.Leu489Ile
ENST00000371953.8:c.946_948delinsATT MANE Select	ENSP00000361021.3:p.Leu316Ile
ENST00000371953.7:c.946_948delinsATT	ENSP00000361021.3:p.Leu316Ile
ENST00000472832.2:c.373_375delinsATT	ENSP00000483066.1:p.Leu125Ile
NM_000314.5:c.946_948delinsATT	NP_000305.3:p.Leu316Ile
NM_000314.6:c.946_948delinsATT	NP_000305.3:p.Leu316Ile
NM_001304717.2:c.1465_1467delinsATT	NP_001291646.2:p.Leu489Ile
NM_001304718.1:c.355_357delinsATT	NP_001291647.1:p.Leu119Ile
XM_006717926.2:c.901_903delinsATT	XP_006717989.1:p.Leu301Ile
XM_011539981.1:c.946_948delinsATT	XP_011538283.1:p.Leu316Ile
XM_011539982.1:c.850_852delinsATT	XP_011538284.1:p.Leu284Ile
XR_945791.1:n.1516_1518delinsATT
NM_000314.7:c.946_948delinsATT	NP_000305.3:p.Leu316Ile
NM_001304717.5:c.1465_1467delinsATT	NP_001291646.4:p.Leu489Ile
NM_001304718.2:c.355_357delinsATT	NP_001291647.1:p.Leu119Ile
NM_000314.8:c.946_948delinsATT MANE Select	NP_000305.3:p.Leu316Ile