Canonical Allele Identifier: CA891837902
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965405_87965406delinsTT , CM000672.2:g.87965405_87965406delinsTT GRCh38
NC_000010.10:g.89725162_89725163delinsTT , CM000672.1:g.89725162_89725163delinsTT GRCh37
NC_000010.9:g.89715142_89715143delinsTT NCBI36
NG_007466.2:g.106967_106968delinsTT , LRG_311:g.106967_106968delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1238_1239delinsTT ENSP00000514759.2:p.Thr413Ile
ENST00000710265.1:c.*174_*175delinsTT ENSP00000518161.1:n.*174_*175delinsTT
ENST00000688158.2:n.1880_1881delinsTT
ENST00000688922.2:c.*975_*976delinsTT ENSP00000508742.2:n.*975_*976delinsTT
ENST00000700021.1:c.1100_1101delinsTT ENSP00000514757.1:p.Thr367Ile
ENST00000700022.1:c.*484_*485delinsTT ENSP00000514758.1:n.*484_*485delinsTT
ENST00000700023.1:n.2303_2304delinsTT
ENST00000700024.1:n.2537_2538delinsTT
ENST00000706954.1:c.1145_1146delinsTT ENSP00000516674.1:p.Thr382Ile
ENST00000706955.1:c.*1180_*1181delinsTT ENSP00000516675.1:n.*1180_*1181delinsTT
ENST00000686459.1:c.*731_*732delinsTT ENSP00000508909.1:n.*731_*732delinsTT
ENST00000688158.1:c.*1256_*1257delinsTT ENSP00000509254.1:n.*1256_*1257delinsTT
ENST00000688308.1:c.1145_1146delinsTT ENSP00000508752.1:p.Thr382Ile
ENST00000688922.1:c.1066_1067delinsTT
ENST00000693560.1:c.1664_1665delinsTT ENSP00000509861.1:p.Thr555Ile
ENST00000371953.8:c.1145_1146delinsTT MANE Select ENSP00000361021.3:p.Thr382Ile
ENST00000371953.7:c.1145_1146delinsTT ENSP00000361021.3:p.Thr382Ile
NM_000314.5:c.1145_1146delinsTT NP_000305.3:p.Thr382Ile
NM_000314.6:c.1145_1146delinsTT NP_000305.3:p.Thr382Ile
NM_001304717.2:c.1664_1665delinsTT NP_001291646.2:p.Thr555Ile
NM_001304718.1:c.554_555delinsTT NP_001291647.1:p.Thr185Ile
XM_006717926.2:c.1100_1101delinsTT XP_006717989.1:p.Thr367Ile
XM_011539982.1:c.1049_1050delinsTT XP_011538284.1:p.Thr350Ile
XR_945791.1:n.1715_1716delinsTT
NM_000314.7:c.1145_1146delinsTT NP_000305.3:p.Thr382Ile
NM_001304717.5:c.1664_1665delinsTT NP_001291646.4:p.Thr555Ile
NM_001304718.2:c.554_555delinsTT NP_001291647.1:p.Thr185Ile
NM_000314.8:c.1145_1146delinsTT MANE Select NP_000305.3:p.Thr382Ile