Canonical Allele Identifier: CA470973975

Gene: PTEN

Linked Data

• COSMIC: COSM5867
• MyVariant Identifiers: chr10:g.89720737del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960980del , CM000672.2:g.87960980del	GRCh38
NC_000010.10:g.89720737del , CM000672.1:g.89720737del	GRCh37
NC_000010.9:g.89710717del	NCBI36
NG_007466.2:g.102542del , LRG_311:g.102542del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.981del	ENSP00000514759.2:p.Cys327TrpfsTer11
ENST00000710265.1:c.888del	ENSP00000518161.1:p.Cys296TrpfsTer11
ENST00000472832.3:c.888del	ENSP00000483066.2:p.Cys296TrpfsTer11
ENST00000688158.2:n.1623del
ENST00000688922.2:c.*718del	ENSP00000508742.2:n.*718del
ENST00000700021.1:c.843del	ENSP00000514757.1:p.Cys281TrpfsTer11
ENST00000700022.1:c.*227del	ENSP00000514758.1:n.*227del
ENST00000700023.1:n.2046del
ENST00000700024.1:n.2280del
ENST00000700025.1:n.1657del
ENST00000700026.1:n.525del
ENST00000706954.1:c.888del	ENSP00000516674.1:p.Cys296TrpfsTer11
ENST00000706955.1:c.*923del	ENSP00000516675.1:n.*923del
ENST00000686459.1:c.*474del	ENSP00000508909.1:n.*474del
ENST00000688158.1:c.*999del	ENSP00000509254.1:n.*999del
ENST00000688308.1:c.888del	ENSP00000508752.1:p.Cys296TrpfsTer11
ENST00000688922.1:c.809del
ENST00000693560.1:c.1407del	ENSP00000509861.1:p.Cys469TrpfsTer11
ENST00000371953.8:c.888del MANE Select	ENSP00000361021.3:p.Cys296TrpfsTer11
ENST00000371953.7:c.888del	ENSP00000361021.3:p.Cys296TrpfsTer11
ENST00000472832.2:c.315del	ENSP00000483066.1:p.Cys105TrpfsTer11
NM_000314.5:c.888del	NP_000305.3:p.Cys296TrpfsTer11
NM_000314.6:c.888del	NP_000305.3:p.Cys296TrpfsTer11
NM_001304717.2:c.1407del	NP_001291646.2:p.Cys469TrpfsTer11
NM_001304718.1:c.297del	NP_001291647.1:p.Cys99TrpfsTer11
XM_006717926.2:c.843del	XP_006717989.1:p.Cys281TrpfsTer11
XM_011539981.1:c.888del	XP_011538283.1:p.Cys296TrpfsTer11
XM_011539982.1:c.792del	XP_011538284.1:p.Cys264TrpfsTer11
XR_945791.1:n.1458del
NM_000314.7:c.888del	NP_000305.3:p.Cys296TrpfsTer11
NM_001304717.5:c.1407del	NP_001291646.4:p.Cys469TrpfsTer11
NM_001304718.2:c.297del	NP_001291647.1:p.Cys99TrpfsTer11
NM_000314.8:c.888del MANE Select	NP_000305.3:p.Cys296TrpfsTer11