Canonical Allele Identifier: CA891837977
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965416_87965417delinsAC , CM000672.2:g.87965416_87965417delinsAC GRCh38
NC_000010.10:g.89725173_89725174delinsAC , CM000672.1:g.89725173_89725174delinsAC GRCh37
NC_000010.9:g.89715153_89715154delinsAC NCBI36
NG_007466.2:g.106978_106979delinsAC , LRG_311:g.106978_106979delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1249_1250delinsAC ENSP00000514759.2:p.Asp417Thr
ENST00000710265.1:c.*185_*186delinsAC ENSP00000518161.1:n.*185_*186delinsAC
ENST00000688158.2:n.1891_1892delinsAC
ENST00000688922.2:c.*986_*987delinsAC ENSP00000508742.2:n.*986_*987delinsAC
ENST00000700021.1:c.1111_1112delinsAC ENSP00000514757.1:p.Asp371Thr
ENST00000700022.1:c.*495_*496delinsAC ENSP00000514758.1:n.*495_*496delinsAC
ENST00000700023.1:n.2314_2315delinsAC
ENST00000700024.1:n.2548_2549delinsAC
ENST00000706954.1:c.1156_1157delinsAC ENSP00000516674.1:p.Asp386Thr
ENST00000706955.1:c.*1191_*1192delinsAC ENSP00000516675.1:n.*1191_*1192delinsAC
ENST00000686459.1:c.*742_*743delinsAC ENSP00000508909.1:n.*742_*743delinsAC
ENST00000688158.1:c.*1267_*1268delinsAC ENSP00000509254.1:n.*1267_*1268delinsAC
ENST00000688308.1:c.1156_1157delinsAC ENSP00000508752.1:p.Asp386Thr
ENST00000688922.1:c.1077_1078delinsAC
ENST00000693560.1:c.1675_1676delinsAC ENSP00000509861.1:p.Asp559Thr
ENST00000371953.8:c.1156_1157delinsAC MANE Select ENSP00000361021.3:p.Asp386Thr
ENST00000371953.7:c.1156_1157delinsAC ENSP00000361021.3:p.Asp386Thr
NM_000314.5:c.1156_1157delinsAC NP_000305.3:p.Asp386Thr
NM_000314.6:c.1156_1157delinsAC NP_000305.3:p.Asp386Thr
NM_001304717.2:c.1675_1676delinsAC NP_001291646.2:p.Asp559Thr
NM_001304718.1:c.565_566delinsAC NP_001291647.1:p.Asp189Thr
XM_006717926.2:c.1111_1112delinsAC XP_006717989.1:p.Asp371Thr
XM_011539982.1:c.1060_1061delinsAC XP_011538284.1:p.Asp354Thr
XR_945791.1:n.1726_1727delinsAC
NM_000314.7:c.1156_1157delinsAC NP_000305.3:p.Asp386Thr
NM_001304717.5:c.1675_1676delinsAC NP_001291646.4:p.Asp559Thr
NM_001304718.2:c.565_566delinsAC NP_001291647.1:p.Asp189Thr
NM_000314.8:c.1156_1157delinsAC MANE Select NP_000305.3:p.Asp386Thr