Canonical Allele Identifier: CA2579926697
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961011_87961013del , CM000672.2:g.87961011_87961013del GRCh38
NC_000010.10:g.89720768_89720770del , CM000672.1:g.89720768_89720770del GRCh37
NC_000010.9:g.89710748_89710750del NCBI36
NG_007466.2:g.102573_102575del , LRG_311:g.102573_102575del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1012_1014del ENSP00000514759.2:p.Glu338del
ENST00000710265.1:c.919_921del ENSP00000518161.1:p.Glu307del
ENST00000472832.3:c.919_921del ENSP00000483066.2:p.Glu307del
ENST00000688158.2:n.1654_1656del
ENST00000688922.2:c.*749_*751del ENSP00000508742.2:n.*749_*751del
ENST00000700021.1:c.874_876del ENSP00000514757.1:p.Glu292del
ENST00000700022.1:c.*258_*260del ENSP00000514758.1:n.*258_*260del
ENST00000700023.1:n.2077_2079del
ENST00000700024.1:n.2311_2313del
ENST00000700025.1:n.1688_1690del
ENST00000700026.1:n.556_558del
ENST00000706954.1:c.919_921del ENSP00000516674.1:p.Glu307del
ENST00000706955.1:c.*954_*956del ENSP00000516675.1:n.*954_*956del
ENST00000686459.1:c.*505_*507del ENSP00000508909.1:n.*505_*507del
ENST00000688158.1:c.*1030_*1032del ENSP00000509254.1:n.*1030_*1032del
ENST00000688308.1:c.919_921del ENSP00000508752.1:p.Glu307del
ENST00000688922.1:c.840_842del
ENST00000693560.1:c.1438_1440del ENSP00000509861.1:p.Glu480del
ENST00000371953.8:c.919_921del MANE Select ENSP00000361021.3:p.Glu307del
ENST00000371953.7:c.919_921del ENSP00000361021.3:p.Glu307del
ENST00000472832.2:c.346_348del ENSP00000483066.1:p.Glu116del
NM_000314.5:c.919_921del NP_000305.3:p.Glu307del
NM_000314.6:c.919_921del NP_000305.3:p.Glu307del
NM_001304717.2:c.1438_1440del NP_001291646.2:p.Glu480del
NM_001304718.1:c.328_330del NP_001291647.1:p.Glu110del
XM_006717926.2:c.874_876del XP_006717989.1:p.Glu292del
XM_011539981.1:c.919_921del XP_011538283.1:p.Glu307del
XM_011539982.1:c.823_825del XP_011538284.1:p.Glu275del
XR_945791.1:n.1489_1491del
NM_000314.7:c.919_921del NP_000305.3:p.Glu307del
NM_001304717.5:c.1438_1440del NP_001291646.4:p.Glu480del
NM_001304718.2:c.328_330del NP_001291647.1:p.Glu110del
NM_000314.8:c.919_921del MANE Select NP_000305.3:p.Glu307del