Canonical Allele Identifier: CA645554112

Gene: PTEN

Linked Data

• COSMIC: COSM87195

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961038_87961060del , CM000672.2:g.87961038_87961060del	GRCh38
NC_000010.10:g.89720795_89720817del , CM000672.1:g.89720795_89720817del	GRCh37
NC_000010.9:g.89710775_89710797del	NCBI36
NG_007466.2:g.102600_102622del , LRG_311:g.102600_102622del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1039_1061del	ENSP00000514759.2:p.Leu347Ter
ENST00000710265.1:c.946_968del	ENSP00000518161.1:p.Leu316Ter
ENST00000472832.3:c.946_968del	ENSP00000483066.2:p.Leu316Ter
ENST00000688158.2:n.1681_1703del
ENST00000688922.2:c.*776_*798del	ENSP00000508742.2:n.*776_*798del
ENST00000700021.1:c.901_923del	ENSP00000514757.1:p.Leu301Ter
ENST00000700022.1:c.*285_*307del	ENSP00000514758.1:n.*285_*307del
ENST00000700023.1:n.2104_2126del
ENST00000700024.1:n.2338_2360del
ENST00000700025.1:n.1715_1737del
ENST00000700026.1:n.583_605del
ENST00000706954.1:c.946_968del	ENSP00000516674.1:p.Leu316Ter
ENST00000706955.1:c.*981_*1003del	ENSP00000516675.1:n.*981_*1003del
ENST00000686459.1:c.*532_*554del	ENSP00000508909.1:n.*532_*554del
ENST00000688158.1:c.*1057_*1079del	ENSP00000509254.1:n.*1057_*1079del
ENST00000688308.1:c.946_968del	ENSP00000508752.1:p.Leu316Ter
ENST00000688922.1:c.867_889del
ENST00000693560.1:c.1465_1487del	ENSP00000509861.1:p.Leu489Ter
ENST00000371953.8:c.946_968del MANE Select	ENSP00000361021.3:p.Leu316Ter
ENST00000371953.7:c.946_968del	ENSP00000361021.3:p.Leu316Ter
ENST00000472832.2:c.373_395del	ENSP00000483066.1:p.Leu125Ter
NM_000314.5:c.946_968del	NP_000305.3:p.Leu316Ter
NM_000314.6:c.946_968del	NP_000305.3:p.Leu316Ter
NM_001304717.2:c.1465_1487del	NP_001291646.2:p.Leu489Ter
NM_001304718.1:c.355_377del	NP_001291647.1:p.Leu119Ter
XM_006717926.2:c.901_923del	XP_006717989.1:p.Leu301Ter
XM_011539981.1:c.946_968del	XP_011538283.1:p.Leu316Ter
XM_011539982.1:c.850_872del	XP_011538284.1:p.Leu284Ter
XR_945791.1:n.1516_1538del
NM_000314.7:c.946_968del	NP_000305.3:p.Leu316Ter
NM_001304717.5:c.1465_1487del	NP_001291646.4:p.Leu489Ter
NM_001304718.2:c.355_377del	NP_001291647.1:p.Leu119Ter
NM_000314.8:c.946_968del MANE Select	NP_000305.3:p.Leu316Ter