Canonical Allele Identifier: CA891836446

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961038_87961040delinsGTT , CM000672.2:g.87961038_87961040delinsGTT	GRCh38
NC_000010.10:g.89720795_89720797delinsGTT , CM000672.1:g.89720795_89720797delinsGTT	GRCh37
NC_000010.9:g.89710775_89710777delinsGTT	NCBI36
NG_007466.2:g.102600_102602delinsGTT , LRG_311:g.102600_102602delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1039_1041delinsGTT	ENSP00000514759.2:p.Leu347Val
ENST00000710265.1:c.946_948delinsGTT	ENSP00000518161.1:p.Leu316Val
ENST00000472832.3:c.946_948delinsGTT	ENSP00000483066.2:p.Leu316Val
ENST00000688158.2:n.1681_1683delinsGTT
ENST00000688922.2:c.*776_*778delinsGTT	ENSP00000508742.2:n.*776_*778delinsGTT
ENST00000700021.1:c.901_903delinsGTT	ENSP00000514757.1:p.Leu301Val
ENST00000700022.1:c.*285_*287delinsGTT	ENSP00000514758.1:n.*285_*287delinsGTT
ENST00000700023.1:n.2104_2106delinsGTT
ENST00000700024.1:n.2338_2340delinsGTT
ENST00000700025.1:n.1715_1717delinsGTT
ENST00000700026.1:n.583_585delinsGTT
ENST00000706954.1:c.946_948delinsGTT	ENSP00000516674.1:p.Leu316Val
ENST00000706955.1:c.*981_*983delinsGTT	ENSP00000516675.1:n.*981_*983delinsGTT
ENST00000686459.1:c.*532_*534delinsGTT	ENSP00000508909.1:n.*532_*534delinsGTT
ENST00000688158.1:c.*1057_*1059delinsGTT	ENSP00000509254.1:n.*1057_*1059delinsGTT
ENST00000688308.1:c.946_948delinsGTT	ENSP00000508752.1:p.Leu316Val
ENST00000688922.1:c.867_869delinsGTT
ENST00000693560.1:c.1465_1467delinsGTT	ENSP00000509861.1:p.Leu489Val
ENST00000371953.8:c.946_948delinsGTT MANE Select	ENSP00000361021.3:p.Leu316Val
ENST00000371953.7:c.946_948delinsGTT	ENSP00000361021.3:p.Leu316Val
ENST00000472832.2:c.373_375delinsGTT	ENSP00000483066.1:p.Leu125Val
NM_000314.5:c.946_948delinsGTT	NP_000305.3:p.Leu316Val
NM_000314.6:c.946_948delinsGTT	NP_000305.3:p.Leu316Val
NM_001304717.2:c.1465_1467delinsGTT	NP_001291646.2:p.Leu489Val
NM_001304718.1:c.355_357delinsGTT	NP_001291647.1:p.Leu119Val
XM_006717926.2:c.901_903delinsGTT	XP_006717989.1:p.Leu301Val
XM_011539981.1:c.946_948delinsGTT	XP_011538283.1:p.Leu316Val
XM_011539982.1:c.850_852delinsGTT	XP_011538284.1:p.Leu284Val
XR_945791.1:n.1516_1518delinsGTT
NM_000314.7:c.946_948delinsGTT	NP_000305.3:p.Leu316Val
NM_001304717.5:c.1465_1467delinsGTT	NP_001291646.4:p.Leu489Val
NM_001304718.2:c.355_357delinsGTT	NP_001291647.1:p.Leu119Val
NM_000314.8:c.946_948delinsGTT MANE Select	NP_000305.3:p.Leu316Val