Canonical Allele Identifier: CA891840070
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958003_87958004delinsTT , CM000672.2:g.87958003_87958004delinsTT GRCh38
NC_000010.10:g.89717760_89717761delinsTT , CM000672.1:g.89717760_89717761delinsTT GRCh37
NC_000010.9:g.89707740_89707741delinsTT NCBI36
NG_007466.2:g.99565_99566delinsTT , LRG_311:g.99565_99566delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.785_786delinsTT ENSP00000514759.2:p.Asn262Ile
ENST00000710265.1:c.785_786delinsTT ENSP00000518161.1:p.Asn262Ile
ENST00000472832.3:c.785_786delinsTT ENSP00000483066.2:p.Asn262Ile
ENST00000688158.2:n.1520_1521delinsTT
ENST00000688922.2:c.*615_*616delinsTT ENSP00000508742.2:n.*615_*616delinsTT
ENST00000700021.1:c.740_741delinsTT ENSP00000514757.1:p.Asn247Ile
ENST00000700022.1:c.*124_*125delinsTT ENSP00000514758.1:n.*124_*125delinsTT
ENST00000700023.1:n.1943_1944delinsTT
ENST00000700024.1:n.2177_2178delinsTT
ENST00000700025.1:n.1554_1555delinsTT
ENST00000700026.1:n.422_423delinsTT
ENST00000700029.1:c.619_620delinsTT
ENST00000706954.1:c.785_786delinsTT ENSP00000516674.1:p.Asn262Ile
ENST00000706955.1:c.*820_*821delinsTT ENSP00000516675.1:n.*820_*821delinsTT
ENST00000686459.1:c.*371_*372delinsTT ENSP00000508909.1:n.*371_*372delinsTT
ENST00000688158.1:c.*896_*897delinsTT ENSP00000509254.1:n.*896_*897delinsTT
ENST00000688308.1:c.785_786delinsTT ENSP00000508752.1:p.Asn262Ile
ENST00000688922.1:c.706_707delinsTT
ENST00000693560.1:c.1304_1305delinsTT ENSP00000509861.1:p.Asn435Ile
ENST00000371953.8:c.785_786delinsTT MANE Select ENSP00000361021.3:p.Asn262Ile
ENST00000371953.7:c.785_786delinsTT ENSP00000361021.3:p.Asn262Ile
ENST00000472832.2:c.212_213delinsTT ENSP00000483066.1:p.Asn71Ile
NM_000314.5:c.785_786delinsTT NP_000305.3:p.Asn262Ile
NM_000314.6:c.785_786delinsTT NP_000305.3:p.Asn262Ile
NM_001304717.2:c.1304_1305delinsTT NP_001291646.2:p.Asn435Ile
NM_001304718.1:c.194_195delinsTT NP_001291647.1:p.Asn65Ile
XM_006717926.2:c.740_741delinsTT XP_006717989.1:p.Asn247Ile
XM_011539981.1:c.785_786delinsTT XP_011538283.1:p.Asn262Ile
XM_011539982.1:c.689_690delinsTT XP_011538284.1:p.Asn230Ile
XR_945791.1:n.1355_1356delinsTT
NM_000314.7:c.785_786delinsTT NP_000305.3:p.Asn262Ile
NM_001304717.5:c.1304_1305delinsTT NP_001291646.4:p.Asn435Ile
NM_001304718.2:c.194_195delinsTT NP_001291647.1:p.Asn65Ile
NM_000314.8:c.785_786delinsTT MANE Select NP_000305.3:p.Asn262Ile