Canonical Allele Identifier: CA645545319
Gene: PTEN HGNC NCBI

Linked Data

COSMIC: COSM4936

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965300_87965301del , CM000672.2:g.87965300_87965301del GRCh38
NC_000010.10:g.89725057_89725058del , CM000672.1:g.89725057_89725058del GRCh37
NC_000010.9:g.89715037_89715038del NCBI36
NG_007466.2:g.106862_106863del , LRG_311:g.106862_106863del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1133_1134del ENSP00000514759.2:p.Phe378TyrfsTer13
ENST00000710265.1:c.*69_*70del ENSP00000518161.1:n.*69_*70del
ENST00000688158.2:n.1775_1776del
ENST00000688922.2:c.*870_*871del ENSP00000508742.2:n.*870_*871del
ENST00000700021.1:c.995_996del ENSP00000514757.1:p.Phe332TyrfsTer13
ENST00000700022.1:c.*379_*380del ENSP00000514758.1:n.*379_*380del
ENST00000700023.1:n.2198_2199del
ENST00000700024.1:n.2432_2433del
ENST00000706954.1:c.1040_1041del ENSP00000516674.1:p.Phe347TyrfsTer13
ENST00000706955.1:c.*1075_*1076del ENSP00000516675.1:n.*1075_*1076del
ENST00000686459.1:c.*626_*627del ENSP00000508909.1:n.*626_*627del
ENST00000688158.1:c.*1151_*1152del ENSP00000509254.1:n.*1151_*1152del
ENST00000688308.1:c.1040_1041del ENSP00000508752.1:p.Phe347TyrfsTer13
ENST00000688922.1:c.961_962del
ENST00000693560.1:c.1559_1560del ENSP00000509861.1:p.Phe520TyrfsTer13
ENST00000371953.8:c.1040_1041del MANE Select ENSP00000361021.3:p.Phe347TyrfsTer13
ENST00000371953.7:c.1040_1041del ENSP00000361021.3:p.Phe347TyrfsTer13
NM_000314.5:c.1040_1041del NP_000305.3:p.Phe347TyrfsTer13
NM_000314.6:c.1040_1041del NP_000305.3:p.Phe347TyrfsTer13
NM_001304717.2:c.1559_1560del NP_001291646.2:p.Phe520TyrfsTer13
NM_001304718.1:c.449_450del NP_001291647.1:p.Phe150TyrfsTer13
XM_006717926.2:c.995_996del XP_006717989.1:p.Phe332TyrfsTer13
XM_011539982.1:c.944_945del XP_011538284.1:p.Phe315TyrfsTer13
XR_945791.1:n.1610_1611del
NM_000314.7:c.1040_1041del NP_000305.3:p.Phe347TyrfsTer13
NM_001304717.5:c.1559_1560del NP_001291646.4:p.Phe520TyrfsTer13
NM_001304718.2:c.449_450del NP_001291647.1:p.Phe150TyrfsTer13
NM_000314.8:c.1040_1041del MANE Select NP_000305.3:p.Phe347TyrfsTer13