Canonical Allele Identifier: CA891842889
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960977_87960978del , CM000672.2:g.87960977_87960978del GRCh38
NC_000010.10:g.89720734_89720735del , CM000672.1:g.89720734_89720735del GRCh37
NC_000010.9:g.89710714_89710715del NCBI36
NG_007466.2:g.102539_102540del , LRG_311:g.102539_102540del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.978_979del ENSP00000514759.2:p.Cys327Ter
ENST00000710265.1:c.885_886del ENSP00000518161.1:p.Cys296Ter
ENST00000472832.3:c.885_886del ENSP00000483066.2:p.Cys296Ter
ENST00000688158.2:n.1620_1621del
ENST00000688922.2:c.*715_*716del ENSP00000508742.2:n.*715_*716del
ENST00000700021.1:c.840_841del ENSP00000514757.1:p.Cys281Ter
ENST00000700022.1:c.*224_*225del ENSP00000514758.1:n.*224_*225del
ENST00000700023.1:n.2043_2044del
ENST00000700024.1:n.2277_2278del
ENST00000700025.1:n.1654_1655del
ENST00000700026.1:n.522_523del
ENST00000706954.1:c.885_886del ENSP00000516674.1:p.Cys296Ter
ENST00000706955.1:c.*920_*921del ENSP00000516675.1:n.*920_*921del
ENST00000686459.1:c.*471_*472del ENSP00000508909.1:n.*471_*472del
ENST00000688158.1:c.*996_*997del ENSP00000509254.1:n.*996_*997del
ENST00000688308.1:c.885_886del ENSP00000508752.1:p.Cys296Ter
ENST00000688922.1:c.806_807del
ENST00000693560.1:c.1404_1405del ENSP00000509861.1:p.Cys469Ter
ENST00000371953.8:c.885_886del MANE Select ENSP00000361021.3:p.Cys296Ter
ENST00000371953.7:c.885_886del ENSP00000361021.3:p.Cys296Ter
ENST00000472832.2:c.312_313del ENSP00000483066.1:p.Cys105Ter
NM_000314.5:c.885_886del NP_000305.3:p.Cys296Ter
NM_000314.6:c.885_886del NP_000305.3:p.Cys296Ter
NM_001304717.2:c.1404_1405del NP_001291646.2:p.Cys469Ter
NM_001304718.1:c.294_295del NP_001291647.1:p.Cys99Ter
XM_006717926.2:c.840_841del XP_006717989.1:p.Cys281Ter
XM_011539981.1:c.885_886del XP_011538283.1:p.Cys296Ter
XM_011539982.1:c.789_790del XP_011538284.1:p.Cys264Ter
XR_945791.1:n.1455_1456del
NM_000314.7:c.885_886del NP_000305.3:p.Cys296Ter
NM_001304717.5:c.1404_1405del NP_001291646.4:p.Cys469Ter
NM_001304718.2:c.294_295del NP_001291647.1:p.Cys99Ter
NM_000314.8:c.885_886del MANE Select NP_000305.3:p.Cys296Ter