Canonical Allele Identifier: CA891837912
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965407_87965408delinsTG , CM000672.2:g.87965407_87965408delinsTG GRCh38
NC_000010.10:g.89725164_89725165delinsTG , CM000672.1:g.89725164_89725165delinsTG GRCh37
NC_000010.9:g.89715144_89715145delinsTG NCBI36
NG_007466.2:g.106969_106970delinsTG , LRG_311:g.106969_106970delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1240_1241delinsTG ENSP00000514759.2:p.Thr414Cys
ENST00000710265.1:c.*176_*177delinsTG ENSP00000518161.1:n.*176_*177delinsTG
ENST00000688158.2:n.1882_1883delinsTG
ENST00000688922.2:c.*977_*978delinsTG ENSP00000508742.2:n.*977_*978delinsTG
ENST00000700021.1:c.1102_1103delinsTG ENSP00000514757.1:p.Thr368Cys
ENST00000700022.1:c.*486_*487delinsTG ENSP00000514758.1:n.*486_*487delinsTG
ENST00000700023.1:n.2305_2306delinsTG
ENST00000700024.1:n.2539_2540delinsTG
ENST00000706954.1:c.1147_1148delinsTG ENSP00000516674.1:p.Thr383Cys
ENST00000706955.1:c.*1182_*1183delinsTG ENSP00000516675.1:n.*1182_*1183delinsTG
ENST00000686459.1:c.*733_*734delinsTG ENSP00000508909.1:n.*733_*734delinsTG
ENST00000688158.1:c.*1258_*1259delinsTG ENSP00000509254.1:n.*1258_*1259delinsTG
ENST00000688308.1:c.1147_1148delinsTG ENSP00000508752.1:p.Thr383Cys
ENST00000688922.1:c.1068_1069delinsTG
ENST00000693560.1:c.1666_1667delinsTG ENSP00000509861.1:p.Thr556Cys
ENST00000371953.8:c.1147_1148delinsTG MANE Select ENSP00000361021.3:p.Thr383Cys
ENST00000371953.7:c.1147_1148delinsTG ENSP00000361021.3:p.Thr383Cys
NM_000314.5:c.1147_1148delinsTG NP_000305.3:p.Thr383Cys
NM_000314.6:c.1147_1148delinsTG NP_000305.3:p.Thr383Cys
NM_001304717.2:c.1666_1667delinsTG NP_001291646.2:p.Thr556Cys
NM_001304718.1:c.556_557delinsTG NP_001291647.1:p.Thr186Cys
XM_006717926.2:c.1102_1103delinsTG XP_006717989.1:p.Thr368Cys
XM_011539982.1:c.1051_1052delinsTG XP_011538284.1:p.Thr351Cys
XR_945791.1:n.1717_1718delinsTG
NM_000314.7:c.1147_1148delinsTG NP_000305.3:p.Thr383Cys
NM_001304717.5:c.1666_1667delinsTG NP_001291646.4:p.Thr556Cys
NM_001304718.2:c.556_557delinsTG NP_001291647.1:p.Thr186Cys
NM_000314.8:c.1147_1148delinsTG MANE Select NP_000305.3:p.Thr383Cys