Canonical Allele Identifier: CA2695203394
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957952_87957955del , CM000672.2:g.87957952_87957955del GRCh38
NC_000010.10:g.89717709_89717712del , CM000672.1:g.89717709_89717712del GRCh37
NC_000010.9:g.89707689_89707692del NCBI36
NG_007466.2:g.99514_99517del , LRG_311:g.99514_99517del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.734_737del ENSP00000514759.2:p.Gln245ArgfsTer10
ENST00000710265.1:c.734_737del ENSP00000518161.1:p.Gln245ArgfsTer10
ENST00000472832.3:c.734_737del ENSP00000483066.2:p.Gln245ArgfsTer10
ENST00000688158.2:n.1469_1472del
ENST00000688922.2:c.*564_*567del ENSP00000508742.2:n.*564_*567del
ENST00000700021.1:c.689_692del ENSP00000514757.1:p.Gln230ArgfsTer10
ENST00000700022.1:c.*73_*76del ENSP00000514758.1:n.*73_*76del
ENST00000700023.1:n.1892_1895del
ENST00000700024.1:n.2126_2129del
ENST00000700025.1:n.1503_1506del
ENST00000700026.1:n.371_374del
ENST00000700029.1:c.568_571del
ENST00000706954.1:c.734_737del ENSP00000516674.1:p.Gln245ArgfsTer10
ENST00000706955.1:c.*769_*772del ENSP00000516675.1:n.*769_*772del
ENST00000686459.1:c.*320_*323del ENSP00000508909.1:n.*320_*323del
ENST00000688158.1:c.*845_*848del ENSP00000509254.1:n.*845_*848del
ENST00000688308.1:c.734_737del ENSP00000508752.1:p.Gln245ArgfsTer10
ENST00000688922.1:c.655_658del
ENST00000693560.1:c.1253_1256del ENSP00000509861.1:p.Gln418ArgfsTer10
ENST00000371953.8:c.734_737del MANE Select ENSP00000361021.3:p.Gln245ArgfsTer10
ENST00000371953.7:c.734_737del ENSP00000361021.3:p.Gln245ArgfsTer10
ENST00000472832.2:c.161_164del ENSP00000483066.1:p.Gln54ArgfsTer10
NM_000314.5:c.734_737del NP_000305.3:p.Gln245ArgfsTer10
NM_000314.6:c.734_737del NP_000305.3:p.Gln245ArgfsTer10
NM_001304717.2:c.1253_1256del NP_001291646.2:p.Gln418ArgfsTer10
NM_001304718.1:c.143_146del NP_001291647.1:p.Gln48ArgfsTer10
XM_006717926.2:c.689_692del XP_006717989.1:p.Gln230ArgfsTer10
XM_011539981.1:c.734_737del XP_011538283.1:p.Gln245ArgfsTer10
XM_011539982.1:c.638_641del XP_011538284.1:p.Gln213ArgfsTer10
XR_945791.1:n.1304_1307del
NM_000314.7:c.734_737del NP_000305.3:p.Gln245ArgfsTer10
NM_001304717.5:c.1253_1256del NP_001291646.4:p.Gln418ArgfsTer10
NM_001304718.2:c.143_146del NP_001291647.1:p.Gln48ArgfsTer10
NM_000314.8:c.734_737del MANE Select NP_000305.3:p.Gln245ArgfsTer10