Canonical Allele Identifier: CA891839903
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957969_87957970delinsTT , CM000672.2:g.87957969_87957970delinsTT GRCh38
NC_000010.10:g.89717726_89717727delinsTT , CM000672.1:g.89717726_89717727delinsTT GRCh37
NC_000010.9:g.89707706_89707707delinsTT NCBI36
NG_007466.2:g.99531_99532delinsTT , LRG_311:g.99531_99532delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.751_752delinsTT ENSP00000514759.2:p.Gly251Phe
ENST00000710265.1:c.751_752delinsTT ENSP00000518161.1:p.Gly251Phe
ENST00000472832.3:c.751_752delinsTT ENSP00000483066.2:p.Gly251Phe
ENST00000688158.2:n.1486_1487delinsTT
ENST00000688922.2:c.*581_*582delinsTT ENSP00000508742.2:n.*581_*582delinsTT
ENST00000700021.1:c.706_707delinsTT ENSP00000514757.1:p.Gly236Phe
ENST00000700022.1:c.*90_*91delinsTT ENSP00000514758.1:n.*90_*91delinsTT
ENST00000700023.1:n.1909_1910delinsTT
ENST00000700024.1:n.2143_2144delinsTT
ENST00000700025.1:n.1520_1521delinsTT
ENST00000700026.1:n.388_389delinsTT
ENST00000700029.1:c.585_586delinsTT
ENST00000706954.1:c.751_752delinsTT ENSP00000516674.1:p.Gly251Phe
ENST00000706955.1:c.*786_*787delinsTT ENSP00000516675.1:n.*786_*787delinsTT
ENST00000686459.1:c.*337_*338delinsTT ENSP00000508909.1:n.*337_*338delinsTT
ENST00000688158.1:c.*862_*863delinsTT ENSP00000509254.1:n.*862_*863delinsTT
ENST00000688308.1:c.751_752delinsTT ENSP00000508752.1:p.Gly251Phe
ENST00000688922.1:c.672_673delinsTT
ENST00000693560.1:c.1270_1271delinsTT ENSP00000509861.1:p.Gly424Phe
ENST00000371953.8:c.751_752delinsTT MANE Select ENSP00000361021.3:p.Gly251Phe
ENST00000371953.7:c.751_752delinsTT ENSP00000361021.3:p.Gly251Phe
ENST00000472832.2:c.178_179delinsTT ENSP00000483066.1:p.Gly60Phe
NM_000314.5:c.751_752delinsTT NP_000305.3:p.Gly251Phe
NM_000314.6:c.751_752delinsTT NP_000305.3:p.Gly251Phe
NM_001304717.2:c.1270_1271delinsTT NP_001291646.2:p.Gly424Phe
NM_001304718.1:c.160_161delinsTT NP_001291647.1:p.Gly54Phe
XM_006717926.2:c.706_707delinsTT XP_006717989.1:p.Gly236Phe
XM_011539981.1:c.751_752delinsTT XP_011538283.1:p.Gly251Phe
XM_011539982.1:c.655_656delinsTT XP_011538284.1:p.Gly219Phe
XR_945791.1:n.1321_1322delinsTT
NM_000314.7:c.751_752delinsTT NP_000305.3:p.Gly251Phe
NM_001304717.5:c.1270_1271delinsTT NP_001291646.4:p.Gly424Phe
NM_001304718.2:c.160_161delinsTT NP_001291647.1:p.Gly54Phe
NM_000314.8:c.751_752delinsTT MANE Select NP_000305.3:p.Gly251Phe