Canonical Allele Identifier: CA2579926790
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957963_87957965del , CM000672.2:g.87957963_87957965del GRCh38
NC_000010.10:g.89717720_89717722del , CM000672.1:g.89717720_89717722del GRCh37
NC_000010.9:g.89707700_89707702del NCBI36
NG_007466.2:g.99525_99527del , LRG_311:g.99525_99527del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.745_747del ENSP00000514759.2:p.Val249del
ENST00000710265.1:c.745_747del ENSP00000518161.1:p.Val249del
ENST00000472832.3:c.745_747del ENSP00000483066.2:p.Val249del
ENST00000688158.2:n.1480_1482del
ENST00000688922.2:c.*575_*577del ENSP00000508742.2:n.*575_*577del
ENST00000700021.1:c.700_702del ENSP00000514757.1:p.Val234del
ENST00000700022.1:c.*84_*86del ENSP00000514758.1:n.*84_*86del
ENST00000700023.1:n.1903_1905del
ENST00000700024.1:n.2137_2139del
ENST00000700025.1:n.1514_1516del
ENST00000700026.1:n.382_384del
ENST00000700029.1:c.579_581del
ENST00000706954.1:c.745_747del ENSP00000516674.1:p.Val249del
ENST00000706955.1:c.*780_*782del ENSP00000516675.1:n.*780_*782del
ENST00000686459.1:c.*331_*333del ENSP00000508909.1:n.*331_*333del
ENST00000688158.1:c.*856_*858del ENSP00000509254.1:n.*856_*858del
ENST00000688308.1:c.745_747del ENSP00000508752.1:p.Val249del
ENST00000688922.1:c.666_668del
ENST00000693560.1:c.1264_1266del ENSP00000509861.1:p.Val422del
ENST00000371953.8:c.745_747del MANE Select ENSP00000361021.3:p.Val249del
ENST00000371953.7:c.745_747del ENSP00000361021.3:p.Val249del
ENST00000472832.2:c.172_174del ENSP00000483066.1:p.Val58del
NM_000314.5:c.745_747del NP_000305.3:p.Val249del
NM_000314.6:c.745_747del NP_000305.3:p.Val249del
NM_001304717.2:c.1264_1266del NP_001291646.2:p.Val422del
NM_001304718.1:c.154_156del NP_001291647.1:p.Val52del
XM_006717926.2:c.700_702del XP_006717989.1:p.Val234del
XM_011539981.1:c.745_747del XP_011538283.1:p.Val249del
XM_011539982.1:c.649_651del XP_011538284.1:p.Val217del
XR_945791.1:n.1315_1317del
NM_000314.7:c.745_747del NP_000305.3:p.Val249del
NM_001304717.5:c.1264_1266del NP_001291646.4:p.Val422del
NM_001304718.2:c.154_156del NP_001291647.1:p.Val52del
NM_000314.8:c.745_747del MANE Select NP_000305.3:p.Val249del