Canonical Allele Identifier: CA891840035
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957997_87957998delinsTT , CM000672.2:g.87957997_87957998delinsTT GRCh38
NC_000010.10:g.89717754_89717755delinsTT , CM000672.1:g.89717754_89717755delinsTT GRCh37
NC_000010.9:g.89707734_89707735delinsTT NCBI36
NG_007466.2:g.99559_99560delinsTT , LRG_311:g.99559_99560delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.779_780delinsTT ENSP00000514759.2:p.Lys260Ile
ENST00000710265.1:c.779_780delinsTT ENSP00000518161.1:p.Lys260Ile
ENST00000472832.3:c.779_780delinsTT ENSP00000483066.2:p.Lys260Ile
ENST00000688158.2:n.1514_1515delinsTT
ENST00000688922.2:c.*609_*610delinsTT ENSP00000508742.2:n.*609_*610delinsTT
ENST00000700021.1:c.734_735delinsTT ENSP00000514757.1:p.Lys245Ile
ENST00000700022.1:c.*118_*119delinsTT ENSP00000514758.1:n.*118_*119delinsTT
ENST00000700023.1:n.1937_1938delinsTT
ENST00000700024.1:n.2171_2172delinsTT
ENST00000700025.1:n.1548_1549delinsTT
ENST00000700026.1:n.416_417delinsTT
ENST00000700029.1:c.613_614delinsTT
ENST00000706954.1:c.779_780delinsTT ENSP00000516674.1:p.Lys260Ile
ENST00000706955.1:c.*814_*815delinsTT ENSP00000516675.1:n.*814_*815delinsTT
ENST00000686459.1:c.*365_*366delinsTT ENSP00000508909.1:n.*365_*366delinsTT
ENST00000688158.1:c.*890_*891delinsTT ENSP00000509254.1:n.*890_*891delinsTT
ENST00000688308.1:c.779_780delinsTT ENSP00000508752.1:p.Lys260Ile
ENST00000688922.1:c.700_701delinsTT
ENST00000693560.1:c.1298_1299delinsTT ENSP00000509861.1:p.Lys433Ile
ENST00000371953.8:c.779_780delinsTT MANE Select ENSP00000361021.3:p.Lys260Ile
ENST00000371953.7:c.779_780delinsTT ENSP00000361021.3:p.Lys260Ile
ENST00000472832.2:c.206_207delinsTT ENSP00000483066.1:p.Lys69Ile
NM_000314.5:c.779_780delinsTT NP_000305.3:p.Lys260Ile
NM_000314.6:c.779_780delinsTT NP_000305.3:p.Lys260Ile
NM_001304717.2:c.1298_1299delinsTT NP_001291646.2:p.Lys433Ile
NM_001304718.1:c.188_189delinsTT NP_001291647.1:p.Lys63Ile
XM_006717926.2:c.734_735delinsTT XP_006717989.1:p.Lys245Ile
XM_011539981.1:c.779_780delinsTT XP_011538283.1:p.Lys260Ile
XM_011539982.1:c.683_684delinsTT XP_011538284.1:p.Lys228Ile
XR_945791.1:n.1349_1350delinsTT
NM_000314.7:c.779_780delinsTT NP_000305.3:p.Lys260Ile
NM_001304717.5:c.1298_1299delinsTT NP_001291646.4:p.Lys433Ile
NM_001304718.2:c.188_189delinsTT NP_001291647.1:p.Lys63Ile
NM_000314.8:c.779_780delinsTT MANE Select NP_000305.3:p.Lys260Ile