Canonical Allele Identifier: CA891841644
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965416_87965417delinsCT , CM000672.2:g.87965416_87965417delinsCT GRCh38
NC_000010.10:g.89725173_89725174delinsCT , CM000672.1:g.89725173_89725174delinsCT GRCh37
NC_000010.9:g.89715153_89715154delinsCT NCBI36
NG_007466.2:g.106978_106979delinsCT , LRG_311:g.106978_106979delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1249_1250delinsCT ENSP00000514759.2:p.Asp417Leu
ENST00000710265.1:c.*185_*186delinsCT ENSP00000518161.1:n.*185_*186delinsCT
ENST00000688158.2:n.1891_1892delinsCT
ENST00000688922.2:c.*986_*987delinsCT ENSP00000508742.2:n.*986_*987delinsCT
ENST00000700021.1:c.1111_1112delinsCT ENSP00000514757.1:p.Asp371Leu
ENST00000700022.1:c.*495_*496delinsCT ENSP00000514758.1:n.*495_*496delinsCT
ENST00000700023.1:n.2314_2315delinsCT
ENST00000700024.1:n.2548_2549delinsCT
ENST00000706954.1:c.1156_1157delinsCT ENSP00000516674.1:p.Asp386Leu
ENST00000706955.1:c.*1191_*1192delinsCT ENSP00000516675.1:n.*1191_*1192delinsCT
ENST00000686459.1:c.*742_*743delinsCT ENSP00000508909.1:n.*742_*743delinsCT
ENST00000688158.1:c.*1267_*1268delinsCT ENSP00000509254.1:n.*1267_*1268delinsCT
ENST00000688308.1:c.1156_1157delinsCT ENSP00000508752.1:p.Asp386Leu
ENST00000688922.1:c.1077_1078delinsCT
ENST00000693560.1:c.1675_1676delinsCT ENSP00000509861.1:p.Asp559Leu
ENST00000371953.8:c.1156_1157delinsCT MANE Select ENSP00000361021.3:p.Asp386Leu
ENST00000371953.7:c.1156_1157delinsCT ENSP00000361021.3:p.Asp386Leu
NM_000314.5:c.1156_1157delinsCT NP_000305.3:p.Asp386Leu
NM_000314.6:c.1156_1157delinsCT NP_000305.3:p.Asp386Leu
NM_001304717.2:c.1675_1676delinsCT NP_001291646.2:p.Asp559Leu
NM_001304718.1:c.565_566delinsCT NP_001291647.1:p.Asp189Leu
XM_006717926.2:c.1111_1112delinsCT XP_006717989.1:p.Asp371Leu
XM_011539982.1:c.1060_1061delinsCT XP_011538284.1:p.Asp354Leu
XR_945791.1:n.1726_1727delinsCT
NM_000314.7:c.1156_1157delinsCT NP_000305.3:p.Asp386Leu
NM_001304717.5:c.1675_1676delinsCT NP_001291646.4:p.Asp559Leu
NM_001304718.2:c.565_566delinsCT NP_001291647.1:p.Asp189Leu
NM_000314.8:c.1156_1157delinsCT MANE Select NP_000305.3:p.Asp386Leu