Canonical Allele Identifier: CA645554067
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958008del , CM000672.2:g.87958008del GRCh38
NC_000010.10:g.89717765del , CM000672.1:g.89717765del GRCh37
NC_000010.9:g.89707745del NCBI36
NG_007466.2:g.99570del , LRG_311:g.99570del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.790del ENSP00000514759.2:p.Met264CysfsTer2
ENST00000710265.1:c.790del ENSP00000518161.1:p.Met264CysfsTer2
ENST00000472832.3:c.790del ENSP00000483066.2:p.Met264CysfsTer2
ENST00000688158.2:n.1525del
ENST00000688922.2:c.*620del ENSP00000508742.2:n.*620del
ENST00000700021.1:c.745del ENSP00000514757.1:p.Met249CysfsTer2
ENST00000700022.1:c.*129del ENSP00000514758.1:n.*129del
ENST00000700023.1:n.1948del
ENST00000700024.1:n.2182del
ENST00000700025.1:n.1559del
ENST00000700026.1:n.427del
ENST00000700029.1:c.624del
ENST00000706954.1:c.790del ENSP00000516674.1:p.Met264CysfsTer2
ENST00000706955.1:c.*825del ENSP00000516675.1:n.*825del
ENST00000686459.1:c.*376del ENSP00000508909.1:n.*376del
ENST00000688158.1:c.*901del ENSP00000509254.1:n.*901del
ENST00000688308.1:c.790del ENSP00000508752.1:p.Met264CysfsTer2
ENST00000688922.1:c.711del
ENST00000693560.1:c.1309del ENSP00000509861.1:p.Met437CysfsTer2
ENST00000371953.8:c.790del MANE Select ENSP00000361021.3:p.Met264CysfsTer2
ENST00000371953.7:c.790del ENSP00000361021.3:p.Met264CysfsTer2
ENST00000472832.2:c.217del ENSP00000483066.1:p.Met73CysfsTer2
NM_000314.5:c.790del NP_000305.3:p.Met264CysfsTer2
NM_000314.6:c.790del NP_000305.3:p.Met264CysfsTer2
NM_001304717.2:c.1309del NP_001291646.2:p.Met437CysfsTer2
NM_001304718.1:c.199del NP_001291647.1:p.Met67CysfsTer2
XM_006717926.2:c.745del XP_006717989.1:p.Met249CysfsTer2
XM_011539981.1:c.790del XP_011538283.1:p.Met264CysfsTer2
XM_011539982.1:c.694del XP_011538284.1:p.Met232CysfsTer2
XR_945791.1:n.1360del
NM_000314.7:c.790del NP_000305.3:p.Met264CysfsTer2
NM_001304717.5:c.1309del NP_001291646.4:p.Met437CysfsTer2
NM_001304718.2:c.199del NP_001291647.1:p.Met67CysfsTer2
NM_000314.8:c.790del MANE Select NP_000305.3:p.Met264CysfsTer2