Canonical Allele Identifier: CA2579926787
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957966_87957968del , CM000672.2:g.87957966_87957968del GRCh38
NC_000010.10:g.89717723_89717725del , CM000672.1:g.89717723_89717725del GRCh37
NC_000010.9:g.89707703_89707705del NCBI36
NG_007466.2:g.99528_99530del , LRG_311:g.99528_99530del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.748_750del ENSP00000514759.2:p.Cys250del
ENST00000710265.1:c.748_750del ENSP00000518161.1:p.Cys250del
ENST00000472832.3:c.748_750del ENSP00000483066.2:p.Cys250del
ENST00000688158.2:n.1483_1485del
ENST00000688922.2:c.*578_*580del ENSP00000508742.2:n.*578_*580del
ENST00000700021.1:c.703_705del ENSP00000514757.1:p.Cys235del
ENST00000700022.1:c.*87_*89del ENSP00000514758.1:n.*87_*89del
ENST00000700023.1:n.1906_1908del
ENST00000700024.1:n.2140_2142del
ENST00000700025.1:n.1517_1519del
ENST00000700026.1:n.385_387del
ENST00000700029.1:c.582_584del
ENST00000706954.1:c.748_750del ENSP00000516674.1:p.Cys250del
ENST00000706955.1:c.*783_*785del ENSP00000516675.1:n.*783_*785del
ENST00000686459.1:c.*334_*336del ENSP00000508909.1:n.*334_*336del
ENST00000688158.1:c.*859_*861del ENSP00000509254.1:n.*859_*861del
ENST00000688308.1:c.748_750del ENSP00000508752.1:p.Cys250del
ENST00000688922.1:c.669_671del
ENST00000693560.1:c.1267_1269del ENSP00000509861.1:p.Cys423del
ENST00000371953.8:c.748_750del MANE Select ENSP00000361021.3:p.Cys250del
ENST00000371953.7:c.748_750del ENSP00000361021.3:p.Cys250del
ENST00000472832.2:c.175_177del ENSP00000483066.1:p.Cys59del
NM_000314.5:c.748_750del NP_000305.3:p.Cys250del
NM_000314.6:c.748_750del NP_000305.3:p.Cys250del
NM_001304717.2:c.1267_1269del NP_001291646.2:p.Cys423del
NM_001304718.1:c.157_159del NP_001291647.1:p.Cys53del
XM_006717926.2:c.703_705del XP_006717989.1:p.Cys235del
XM_011539981.1:c.748_750del XP_011538283.1:p.Cys250del
XM_011539982.1:c.652_654del XP_011538284.1:p.Cys218del
XR_945791.1:n.1318_1320del
NM_000314.7:c.748_750del NP_000305.3:p.Cys250del
NM_001304717.5:c.1267_1269del NP_001291646.4:p.Cys423del
NM_001304718.2:c.157_159del NP_001291647.1:p.Cys53del
NM_000314.8:c.748_750del MANE Select NP_000305.3:p.Cys250del