Canonical Allele Identifier: CA891837899
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965404_87965406delinsGTT , CM000672.2:g.87965404_87965406delinsGTT GRCh38
NC_000010.10:g.89725161_89725163delinsGTT , CM000672.1:g.89725161_89725163delinsGTT GRCh37
NC_000010.9:g.89715141_89715143delinsGTT NCBI36
NG_007466.2:g.106966_106968delinsGTT , LRG_311:g.106966_106968delinsGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1237_1239delinsGTT ENSP00000514759.2:p.Thr413Val
ENST00000710265.1:c.*173_*175delinsGTT ENSP00000518161.1:n.*173_*175delinsGTT
ENST00000688158.2:n.1879_1881delinsGTT
ENST00000688922.2:c.*974_*976delinsGTT ENSP00000508742.2:n.*974_*976delinsGTT
ENST00000700021.1:c.1099_1101delinsGTT ENSP00000514757.1:p.Thr367Val
ENST00000700022.1:c.*483_*485delinsGTT ENSP00000514758.1:n.*483_*485delinsGTT
ENST00000700023.1:n.2302_2304delinsGTT
ENST00000700024.1:n.2536_2538delinsGTT
ENST00000706954.1:c.1144_1146delinsGTT ENSP00000516674.1:p.Thr382Val
ENST00000706955.1:c.*1179_*1181delinsGTT ENSP00000516675.1:n.*1179_*1181delinsGTT
ENST00000686459.1:c.*730_*732delinsGTT ENSP00000508909.1:n.*730_*732delinsGTT
ENST00000688158.1:c.*1255_*1257delinsGTT ENSP00000509254.1:n.*1255_*1257delinsGTT
ENST00000688308.1:c.1144_1146delinsGTT ENSP00000508752.1:p.Thr382Val
ENST00000688922.1:c.1065_1067delinsGTT
ENST00000693560.1:c.1663_1665delinsGTT ENSP00000509861.1:p.Thr555Val
ENST00000371953.8:c.1144_1146delinsGTT MANE Select ENSP00000361021.3:p.Thr382Val
ENST00000371953.7:c.1144_1146delinsGTT ENSP00000361021.3:p.Thr382Val
NM_000314.5:c.1144_1146delinsGTT NP_000305.3:p.Thr382Val
NM_000314.6:c.1144_1146delinsGTT NP_000305.3:p.Thr382Val
NM_001304717.2:c.1663_1665delinsGTT NP_001291646.2:p.Thr555Val
NM_001304718.1:c.553_555delinsGTT NP_001291647.1:p.Thr185Val
XM_006717926.2:c.1099_1101delinsGTT XP_006717989.1:p.Thr367Val
XM_011539982.1:c.1048_1050delinsGTT XP_011538284.1:p.Thr350Val
XR_945791.1:n.1714_1716delinsGTT
NM_000314.7:c.1144_1146delinsGTT NP_000305.3:p.Thr382Val
NM_001304717.5:c.1663_1665delinsGTT NP_001291646.4:p.Thr555Val
NM_001304718.2:c.553_555delinsGTT NP_001291647.1:p.Thr185Val
NM_000314.8:c.1144_1146delinsGTT MANE Select NP_000305.3:p.Thr382Val