Canonical Allele Identifier: CA891837969
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965416_87965417delinsTG , CM000672.2:g.87965416_87965417delinsTG GRCh38
NC_000010.10:g.89725173_89725174delinsTG , CM000672.1:g.89725173_89725174delinsTG GRCh37
NC_000010.9:g.89715153_89715154delinsTG NCBI36
NG_007466.2:g.106978_106979delinsTG , LRG_311:g.106978_106979delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1249_1250delinsTG ENSP00000514759.2:p.Asp417Cys
ENST00000710265.1:c.*185_*186delinsTG ENSP00000518161.1:n.*185_*186delinsTG
ENST00000688158.2:n.1891_1892delinsTG
ENST00000688922.2:c.*986_*987delinsTG ENSP00000508742.2:n.*986_*987delinsTG
ENST00000700021.1:c.1111_1112delinsTG ENSP00000514757.1:p.Asp371Cys
ENST00000700022.1:c.*495_*496delinsTG ENSP00000514758.1:n.*495_*496delinsTG
ENST00000700023.1:n.2314_2315delinsTG
ENST00000700024.1:n.2548_2549delinsTG
ENST00000706954.1:c.1156_1157delinsTG ENSP00000516674.1:p.Asp386Cys
ENST00000706955.1:c.*1191_*1192delinsTG ENSP00000516675.1:n.*1191_*1192delinsTG
ENST00000686459.1:c.*742_*743delinsTG ENSP00000508909.1:n.*742_*743delinsTG
ENST00000688158.1:c.*1267_*1268delinsTG ENSP00000509254.1:n.*1267_*1268delinsTG
ENST00000688308.1:c.1156_1157delinsTG ENSP00000508752.1:p.Asp386Cys
ENST00000688922.1:c.1077_1078delinsTG
ENST00000693560.1:c.1675_1676delinsTG ENSP00000509861.1:p.Asp559Cys
ENST00000371953.8:c.1156_1157delinsTG MANE Select ENSP00000361021.3:p.Asp386Cys
ENST00000371953.7:c.1156_1157delinsTG ENSP00000361021.3:p.Asp386Cys
NM_000314.5:c.1156_1157delinsTG NP_000305.3:p.Asp386Cys
NM_000314.6:c.1156_1157delinsTG NP_000305.3:p.Asp386Cys
NM_001304717.2:c.1675_1676delinsTG NP_001291646.2:p.Asp559Cys
NM_001304718.1:c.565_566delinsTG NP_001291647.1:p.Asp189Cys
XM_006717926.2:c.1111_1112delinsTG XP_006717989.1:p.Asp371Cys
XM_011539982.1:c.1060_1061delinsTG XP_011538284.1:p.Asp354Cys
XR_945791.1:n.1726_1727delinsTG
NM_000314.7:c.1156_1157delinsTG NP_000305.3:p.Asp386Cys
NM_001304717.5:c.1675_1676delinsTG NP_001291646.4:p.Asp559Cys
NM_001304718.2:c.565_566delinsTG NP_001291647.1:p.Asp189Cys
NM_000314.8:c.1156_1157delinsTG MANE Select NP_000305.3:p.Asp386Cys