Canonical Allele Identifier: CA2579926875
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957952_87957954del , CM000672.2:g.87957952_87957954del GRCh38
NC_000010.10:g.89717709_89717711del , CM000672.1:g.89717709_89717711del GRCh37
NC_000010.9:g.89707689_89707691del NCBI36
NG_007466.2:g.99514_99516del , LRG_311:g.99514_99516del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.734_736del ENSP00000514759.2:p.Gln245del
ENST00000710265.1:c.734_736del ENSP00000518161.1:p.Gln245del
ENST00000472832.3:c.734_736del ENSP00000483066.2:p.Gln245del
ENST00000688158.2:n.1469_1471del
ENST00000688922.2:c.*564_*566del ENSP00000508742.2:n.*564_*566del
ENST00000700021.1:c.689_691del ENSP00000514757.1:p.Gln230del
ENST00000700022.1:c.*73_*75del ENSP00000514758.1:n.*73_*75del
ENST00000700023.1:n.1892_1894del
ENST00000700024.1:n.2126_2128del
ENST00000700025.1:n.1503_1505del
ENST00000700026.1:n.371_373del
ENST00000700029.1:c.568_570del
ENST00000706954.1:c.734_736del ENSP00000516674.1:p.Gln245del
ENST00000706955.1:c.*769_*771del ENSP00000516675.1:n.*769_*771del
ENST00000686459.1:c.*320_*322del ENSP00000508909.1:n.*320_*322del
ENST00000688158.1:c.*845_*847del ENSP00000509254.1:n.*845_*847del
ENST00000688308.1:c.734_736del ENSP00000508752.1:p.Gln245del
ENST00000688922.1:c.655_657del
ENST00000693560.1:c.1253_1255del ENSP00000509861.1:p.Gln418del
ENST00000371953.8:c.734_736del MANE Select ENSP00000361021.3:p.Gln245del
ENST00000371953.7:c.734_736del ENSP00000361021.3:p.Gln245del
ENST00000472832.2:c.161_163del ENSP00000483066.1:p.Gln54del
NM_000314.5:c.734_736del NP_000305.3:p.Gln245del
NM_000314.6:c.734_736del NP_000305.3:p.Gln245del
NM_001304717.2:c.1253_1255del NP_001291646.2:p.Gln418del
NM_001304718.1:c.143_145del NP_001291647.1:p.Gln48del
XM_006717926.2:c.689_691del XP_006717989.1:p.Gln230del
XM_011539981.1:c.734_736del XP_011538283.1:p.Gln245del
XM_011539982.1:c.638_640del XP_011538284.1:p.Gln213del
XR_945791.1:n.1304_1306del
NM_000314.7:c.734_736del NP_000305.3:p.Gln245del
NM_001304717.5:c.1253_1255del NP_001291646.4:p.Gln418del
NM_001304718.2:c.143_145del NP_001291647.1:p.Gln48del
NM_000314.8:c.734_736del MANE Select NP_000305.3:p.Gln245del