Canonical Allele Identifier: CA891837895
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965404_87965406delinsTAT , CM000672.2:g.87965404_87965406delinsTAT GRCh38
NC_000010.10:g.89725161_89725163delinsTAT , CM000672.1:g.89725161_89725163delinsTAT GRCh37
NC_000010.9:g.89715141_89715143delinsTAT NCBI36
NG_007466.2:g.106966_106968delinsTAT , LRG_311:g.106966_106968delinsTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1237_1239delinsTAT ENSP00000514759.2:p.Thr413Tyr
ENST00000710265.1:c.*173_*175delinsTAT ENSP00000518161.1:n.*173_*175delinsTAT
ENST00000688158.2:n.1879_1881delinsTAT
ENST00000688922.2:c.*974_*976delinsTAT ENSP00000508742.2:n.*974_*976delinsTAT
ENST00000700021.1:c.1099_1101delinsTAT ENSP00000514757.1:p.Thr367Tyr
ENST00000700022.1:c.*483_*485delinsTAT ENSP00000514758.1:n.*483_*485delinsTAT
ENST00000700023.1:n.2302_2304delinsTAT
ENST00000700024.1:n.2536_2538delinsTAT
ENST00000706954.1:c.1144_1146delinsTAT ENSP00000516674.1:p.Thr382Tyr
ENST00000706955.1:c.*1179_*1181delinsTAT ENSP00000516675.1:n.*1179_*1181delinsTAT
ENST00000686459.1:c.*730_*732delinsTAT ENSP00000508909.1:n.*730_*732delinsTAT
ENST00000688158.1:c.*1255_*1257delinsTAT ENSP00000509254.1:n.*1255_*1257delinsTAT
ENST00000688308.1:c.1144_1146delinsTAT ENSP00000508752.1:p.Thr382Tyr
ENST00000688922.1:c.1065_1067delinsTAT
ENST00000693560.1:c.1663_1665delinsTAT ENSP00000509861.1:p.Thr555Tyr
ENST00000371953.8:c.1144_1146delinsTAT MANE Select ENSP00000361021.3:p.Thr382Tyr
ENST00000371953.7:c.1144_1146delinsTAT ENSP00000361021.3:p.Thr382Tyr
NM_000314.5:c.1144_1146delinsTAT NP_000305.3:p.Thr382Tyr
NM_000314.6:c.1144_1146delinsTAT NP_000305.3:p.Thr382Tyr
NM_001304717.2:c.1663_1665delinsTAT NP_001291646.2:p.Thr555Tyr
NM_001304718.1:c.553_555delinsTAT NP_001291647.1:p.Thr185Tyr
XM_006717926.2:c.1099_1101delinsTAT XP_006717989.1:p.Thr367Tyr
XM_011539982.1:c.1048_1050delinsTAT XP_011538284.1:p.Thr350Tyr
XR_945791.1:n.1714_1716delinsTAT
NM_000314.7:c.1144_1146delinsTAT NP_000305.3:p.Thr382Tyr
NM_001304717.5:c.1663_1665delinsTAT NP_001291646.4:p.Thr555Tyr
NM_001304718.2:c.553_555delinsTAT NP_001291647.1:p.Thr185Tyr
NM_000314.8:c.1144_1146delinsTAT MANE Select NP_000305.3:p.Thr382Tyr