Canonical Allele Identifier: CA645554060
Gene: PTEN HGNC NCBI

Linked Data

COSMIC: COSM4895
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957981_87957994del , CM000672.2:g.87957981_87957994del GRCh38
NC_000010.10:g.89717738_89717751del , CM000672.1:g.89717738_89717751del GRCh37
NC_000010.9:g.89707718_89707731del NCBI36
NG_007466.2:g.99543_99556del , LRG_311:g.99543_99556del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.763_776del ENSP00000514759.2:p.Val255GlnfsTer?
ENST00000710265.1:c.763_776del ENSP00000518161.1:p.Val255GlnfsTer?
ENST00000472832.3:c.763_776del ENSP00000483066.2:p.Val255GlnfsTer?
ENST00000688158.2:n.1498_1511del
ENST00000688922.2:c.*593_*606del ENSP00000508742.2:n.*593_*606del
ENST00000700021.1:c.718_731del ENSP00000514757.1:p.Val240GlnfsTer?
ENST00000700022.1:c.*102_*115del ENSP00000514758.1:n.*102_*115del
ENST00000700023.1:n.1921_1934del
ENST00000700024.1:n.2155_2168del
ENST00000700025.1:n.1532_1545del
ENST00000700026.1:n.400_413del
ENST00000700029.1:c.597_610del
ENST00000706954.1:c.763_776del ENSP00000516674.1:p.Val255GlnfsTer?
ENST00000706955.1:c.*798_*811del ENSP00000516675.1:n.*798_*811del
ENST00000686459.1:c.*349_*362del ENSP00000508909.1:n.*349_*362del
ENST00000688158.1:c.*874_*887del ENSP00000509254.1:n.*874_*887del
ENST00000688308.1:c.763_776del ENSP00000508752.1:p.Val255GlnfsTer?
ENST00000688922.1:c.684_697del
ENST00000693560.1:c.1282_1295del ENSP00000509861.1:p.Val428GlnfsTer?
ENST00000371953.8:c.763_776del MANE Select ENSP00000361021.3:p.Val255GlnfsTer?
ENST00000371953.7:c.763_776del ENSP00000361021.3:p.Val255GlnfsTer?
ENST00000472832.2:c.190_203del ENSP00000483066.1:p.Val64GlnfsTer?
NM_000314.5:c.763_776del NP_000305.3:p.Val255GlnfsTer?
NM_000314.6:c.763_776del NP_000305.3:p.Val255GlnfsTer?
NM_001304717.2:c.1282_1295del NP_001291646.2:p.Val428GlnfsTer?
NM_001304718.1:c.172_185del NP_001291647.1:p.Val58GlnfsTer?
XM_006717926.2:c.718_731del XP_006717989.1:p.Val240GlnfsTer?
XM_011539981.1:c.763_776del XP_011538283.1:p.Val255GlnfsTer?
XM_011539982.1:c.667_680del XP_011538284.1:p.Val223GlnfsTer?
XR_945791.1:n.1333_1346del
NM_000314.7:c.763_776del NP_000305.3:p.Val255GlnfsTer?
NM_001304717.5:c.1282_1295del NP_001291646.4:p.Val428GlnfsTer?
NM_001304718.2:c.172_185del NP_001291647.1:p.Val58GlnfsTer?
NM_000314.8:c.763_776del MANE Select NP_000305.3:p.Val255GlnfsTer?
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