Canonical Allele Identifier: CA891841697
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965449_87965450delinsAC , CM000672.2:g.87965449_87965450delinsAC GRCh38
NC_000010.10:g.89725206_89725207delinsAC , CM000672.1:g.89725206_89725207delinsAC GRCh37
NC_000010.9:g.89715186_89715187delinsAC NCBI36
NG_007466.2:g.107011_107012delinsAC , LRG_311:g.107011_107012delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1282_1283delinsAC ENSP00000514759.2:p.His428Thr
ENST00000710265.1:c.*218_*219delinsAC ENSP00000518161.1:n.*218_*219delinsAC
ENST00000688158.2:n.1924_1925delinsAC
ENST00000688922.2:c.*1019_*1020delinsAC ENSP00000508742.2:n.*1019_*1020delinsAC
ENST00000700021.1:c.1144_1145delinsAC ENSP00000514757.1:p.His382Thr
ENST00000700022.1:c.*528_*529delinsAC ENSP00000514758.1:n.*528_*529delinsAC
ENST00000700023.1:n.2347_2348delinsAC
ENST00000700024.1:n.2581_2582delinsAC
ENST00000706954.1:c.1189_1190delinsAC ENSP00000516674.1:p.His397Thr
ENST00000706955.1:c.*1224_*1225delinsAC ENSP00000516675.1:n.*1224_*1225delinsAC
ENST00000686459.1:c.*775_*776delinsAC ENSP00000508909.1:n.*775_*776delinsAC
ENST00000688158.1:c.*1300_*1301delinsAC ENSP00000509254.1:n.*1300_*1301delinsAC
ENST00000688308.1:c.1189_1190delinsAC ENSP00000508752.1:p.His397Thr
ENST00000688922.1:c.1110_1111delinsAC
ENST00000693560.1:c.1708_1709delinsAC ENSP00000509861.1:p.His570Thr
ENST00000371953.8:c.1189_1190delinsAC MANE Select ENSP00000361021.3:p.His397Thr
ENST00000371953.7:c.1189_1190delinsAC ENSP00000361021.3:p.His397Thr
NM_000314.5:c.1189_1190delinsAC NP_000305.3:p.His397Thr
NM_000314.6:c.1189_1190delinsAC NP_000305.3:p.His397Thr
NM_001304717.2:c.1708_1709delinsAC NP_001291646.2:p.His570Thr
NM_001304718.1:c.598_599delinsAC NP_001291647.1:p.His200Thr
XM_006717926.2:c.1144_1145delinsAC XP_006717989.1:p.His382Thr
XM_011539982.1:c.1093_1094delinsAC XP_011538284.1:p.His365Thr
XR_945791.1:n.1759_1760delinsAC
NM_000314.7:c.1189_1190delinsAC NP_000305.3:p.His397Thr
NM_001304717.5:c.1708_1709delinsAC NP_001291646.4:p.His570Thr
NM_001304718.2:c.598_599delinsAC NP_001291647.1:p.His200Thr
NM_000314.8:c.1189_1190delinsAC MANE Select NP_000305.3:p.His397Thr