Canonical Allele Identifier: CA645553822

Gene: PTEN

Linked Data

• COSMIC: COSM3358389

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933123_87933136del , CM000672.2:g.87933123_87933136del	GRCh38
NC_000010.10:g.89692880_89692893del , CM000672.1:g.89692880_89692893del	GRCh37
NC_000010.9:g.89682860_89682873del	NCBI36
NG_007466.2:g.74685_74698del , LRG_311:g.74685_74698del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.364_377del	ENSP00000514759.2:p.Ile122TrpfsTer?
ENST00000710265.1:c.364_377del	ENSP00000518161.1:p.Ile122TrpfsTer?
ENST00000472832.3:c.364_377del	ENSP00000483066.2:p.Ile122TrpfsTer?
ENST00000688158.2:n.1099_1112del
ENST00000688922.2:c.*194_*207del	ENSP00000508742.2:n.*194_*207del
ENST00000700021.1:c.319_332del	ENSP00000514757.1:p.Ile107TrpfsTer?
ENST00000700022.1:c.364_377del	ENSP00000514758.1:p.Ile122TrpfsTer?
ENST00000700029.1:c.198_211del
ENST00000706954.1:c.364_377del	ENSP00000516674.1:p.Ile122TrpfsTer?
ENST00000706955.1:c.*399_*412del	ENSP00000516675.1:n.*399_*412del
ENST00000686459.1:c.364_377del	ENSP00000508909.1:p.Ile122TrpfsTer?
ENST00000688158.1:c.*475_*488del	ENSP00000509254.1:n.*475_*488del
ENST00000688308.1:c.364_377del	ENSP00000508752.1:p.Ile122TrpfsTer?
ENST00000688922.1:c.285_298del
ENST00000693560.1:c.883_896del	ENSP00000509861.1:p.Ile295TrpfsTer?
ENST00000371953.8:c.364_377del MANE Select	ENSP00000361021.3:p.Ile122TrpfsTer?
ENST00000371953.7:c.364_377del	ENSP00000361021.3:p.Ile122TrpfsTer?
ENST00000498703.1:n.190_203del
ENST00000610634.1:c.262_275del	ENSP00000477517.1:p.Ile88TrpfsTer?
NM_000314.5:c.364_377del	NP_000305.3:p.Ile122TrpfsTer?
NM_000314.6:c.364_377del	NP_000305.3:p.Ile122TrpfsTer?
NM_001304717.2:c.883_896del	NP_001291646.2:p.Ile295TrpfsTer?
NM_001304718.1:c.-387_-374del	NP_001291647.1:n.-387_-374del
XM_006717926.2:c.319_332del	XP_006717989.1:p.Ile107TrpfsTer?
XM_011539981.1:c.364_377del	XP_011538283.1:p.Ile122TrpfsTer?
XM_011539982.1:c.268_281del	XP_011538284.1:p.Ile90TrpfsTer?
XR_945789.1:n.1076_1089del
XR_945790.1:n.1076_1089del
XR_945791.1:n.1076_1089del
NM_000314.7:c.364_377del	NP_000305.3:p.Ile122TrpfsTer?
NM_001304717.5:c.883_896del	NP_001291646.4:p.Ile295TrpfsTer?
NM_001304718.2:c.-387_-374del	NP_001291647.1:n.-387_-374del
NM_000314.8:c.364_377del MANE Select	NP_000305.3:p.Ile122TrpfsTer?