Canonical Allele Identifier: CA891841646
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965416_87965417delinsCG , CM000672.2:g.87965416_87965417delinsCG GRCh38
NC_000010.10:g.89725173_89725174delinsCG , CM000672.1:g.89725173_89725174delinsCG GRCh37
NC_000010.9:g.89715153_89715154delinsCG NCBI36
NG_007466.2:g.106978_106979delinsCG , LRG_311:g.106978_106979delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1249_1250delinsCG ENSP00000514759.2:p.Asp417Arg
ENST00000710265.1:c.*185_*186delinsCG ENSP00000518161.1:n.*185_*186delinsCG
ENST00000688158.2:n.1891_1892delinsCG
ENST00000688922.2:c.*986_*987delinsCG ENSP00000508742.2:n.*986_*987delinsCG
ENST00000700021.1:c.1111_1112delinsCG ENSP00000514757.1:p.Asp371Arg
ENST00000700022.1:c.*495_*496delinsCG ENSP00000514758.1:n.*495_*496delinsCG
ENST00000700023.1:n.2314_2315delinsCG
ENST00000700024.1:n.2548_2549delinsCG
ENST00000706954.1:c.1156_1157delinsCG ENSP00000516674.1:p.Asp386Arg
ENST00000706955.1:c.*1191_*1192delinsCG ENSP00000516675.1:n.*1191_*1192delinsCG
ENST00000686459.1:c.*742_*743delinsCG ENSP00000508909.1:n.*742_*743delinsCG
ENST00000688158.1:c.*1267_*1268delinsCG ENSP00000509254.1:n.*1267_*1268delinsCG
ENST00000688308.1:c.1156_1157delinsCG ENSP00000508752.1:p.Asp386Arg
ENST00000688922.1:c.1077_1078delinsCG
ENST00000693560.1:c.1675_1676delinsCG ENSP00000509861.1:p.Asp559Arg
ENST00000371953.8:c.1156_1157delinsCG MANE Select ENSP00000361021.3:p.Asp386Arg
ENST00000371953.7:c.1156_1157delinsCG ENSP00000361021.3:p.Asp386Arg
NM_000314.5:c.1156_1157delinsCG NP_000305.3:p.Asp386Arg
NM_000314.6:c.1156_1157delinsCG NP_000305.3:p.Asp386Arg
NM_001304717.2:c.1675_1676delinsCG NP_001291646.2:p.Asp559Arg
NM_001304718.1:c.565_566delinsCG NP_001291647.1:p.Asp189Arg
XM_006717926.2:c.1111_1112delinsCG XP_006717989.1:p.Asp371Arg
XM_011539982.1:c.1060_1061delinsCG XP_011538284.1:p.Asp354Arg
XR_945791.1:n.1726_1727delinsCG
NM_000314.7:c.1156_1157delinsCG NP_000305.3:p.Asp386Arg
NM_001304717.5:c.1675_1676delinsCG NP_001291646.4:p.Asp559Arg
NM_001304718.2:c.565_566delinsCG NP_001291647.1:p.Asp189Arg
NM_000314.8:c.1156_1157delinsCG MANE Select NP_000305.3:p.Asp386Arg