Canonical Allele Identifier: CA2579926633
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961092_87961094del , CM000672.2:g.87961092_87961094del GRCh38
NC_000010.10:g.89720849_89720851del , CM000672.1:g.89720849_89720851del GRCh37
NC_000010.9:g.89710829_89710831del NCBI36
NG_007466.2:g.102654_102656del , LRG_311:g.102654_102656del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1093_1095del ENSP00000514759.2:p.Asn365del
ENST00000710265.1:c.1000_1002del ENSP00000518161.1:p.Asn334del
ENST00000472832.3:c.1000_1002del ENSP00000483066.2:p.Asn334del
ENST00000688158.2:n.1735_1737del
ENST00000688922.2:c.*830_*832del ENSP00000508742.2:n.*830_*832del
ENST00000700021.1:c.955_957del ENSP00000514757.1:p.Asn319del
ENST00000700022.1:c.*339_*341del ENSP00000514758.1:n.*339_*341del
ENST00000700023.1:n.2158_2160del
ENST00000700024.1:n.2392_2394del
ENST00000700025.1:n.1769_1771del
ENST00000700026.1:n.637_639del
ENST00000706954.1:c.1000_1002del ENSP00000516674.1:p.Asn334del
ENST00000706955.1:c.*1035_*1037del ENSP00000516675.1:n.*1035_*1037del
ENST00000686459.1:c.*586_*588del ENSP00000508909.1:n.*586_*588del
ENST00000688158.1:c.*1111_*1113del ENSP00000509254.1:n.*1111_*1113del
ENST00000688308.1:c.1000_1002del ENSP00000508752.1:p.Asn334del
ENST00000688922.1:c.921_923del
ENST00000693560.1:c.1519_1521del ENSP00000509861.1:p.Asn507del
ENST00000371953.8:c.1000_1002del MANE Select ENSP00000361021.3:p.Asn334del
ENST00000371953.7:c.1000_1002del ENSP00000361021.3:p.Asn334del
ENST00000472832.2:c.427_429del ENSP00000483066.1:p.Asn143del
NM_000314.5:c.1000_1002del NP_000305.3:p.Asn334del
NM_000314.6:c.1000_1002del NP_000305.3:p.Asn334del
NM_001304717.2:c.1519_1521del NP_001291646.2:p.Asn507del
NM_001304718.1:c.409_411del NP_001291647.1:p.Asn137del
XM_006717926.2:c.955_957del XP_006717989.1:p.Asn319del
XM_011539981.1:c.1000_1002del XP_011538283.1:p.Asn334del
XM_011539982.1:c.904_906del XP_011538284.1:p.Asn302del
XR_945791.1:n.1570_1572del
NM_000314.7:c.1000_1002del NP_000305.3:p.Asn334del
NM_001304717.5:c.1519_1521del NP_001291646.4:p.Asn507del
NM_001304718.2:c.409_411del NP_001291647.1:p.Asn137del
NM_000314.8:c.1000_1002del MANE Select NP_000305.3:p.Asn334del