Canonical Allele Identifier: CA891838235
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965459_87965460delinsGA , CM000672.2:g.87965459_87965460delinsGA GRCh38
NC_000010.10:g.89725216_89725217delinsGA , CM000672.1:g.89725216_89725217delinsGA GRCh37
NC_000010.9:g.89715196_89715197delinsGA NCBI36
NG_007466.2:g.107021_107022delinsGA , LRG_311:g.107021_107022delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1292_1293delinsGA ENSP00000514759.2:p.Ile431Arg
ENST00000710265.1:c.*228_*229delinsGA ENSP00000518161.1:n.*228_*229delinsGA
ENST00000688158.2:n.1934_1935delinsGA
ENST00000688922.2:c.*1029_*1030delinsGA ENSP00000508742.2:n.*1029_*1030delinsGA
ENST00000700021.1:c.1154_1155delinsGA ENSP00000514757.1:p.Ile385Arg
ENST00000700022.1:c.*538_*539delinsGA ENSP00000514758.1:n.*538_*539delinsGA
ENST00000700023.1:n.2357_2358delinsGA
ENST00000700024.1:n.2591_2592delinsGA
ENST00000706954.1:c.1199_1200delinsGA ENSP00000516674.1:p.Ile400Arg
ENST00000706955.1:c.*1234_*1235delinsGA ENSP00000516675.1:n.*1234_*1235delinsGA
ENST00000686459.1:c.*785_*786delinsGA ENSP00000508909.1:n.*785_*786delinsGA
ENST00000688158.1:c.*1310_*1311delinsGA ENSP00000509254.1:n.*1310_*1311delinsGA
ENST00000688308.1:c.1199_1200delinsGA ENSP00000508752.1:p.Ile400Arg
ENST00000688922.1:c.1120_1121delinsGA
ENST00000693560.1:c.1718_1719delinsGA ENSP00000509861.1:p.Ile573Arg
ENST00000371953.8:c.1199_1200delinsGA MANE Select ENSP00000361021.3:p.Ile400Arg
ENST00000371953.7:c.1199_1200delinsGA ENSP00000361021.3:p.Ile400Arg
NM_000314.5:c.1199_1200delinsGA NP_000305.3:p.Ile400Arg
NM_000314.6:c.1199_1200delinsGA NP_000305.3:p.Ile400Arg
NM_001304717.2:c.1718_1719delinsGA NP_001291646.2:p.Ile573Arg
NM_001304718.1:c.608_609delinsGA NP_001291647.1:p.Ile203Arg
XM_006717926.2:c.1154_1155delinsGA XP_006717989.1:p.Ile385Arg
XM_011539982.1:c.1103_1104delinsGA XP_011538284.1:p.Ile368Arg
XR_945791.1:n.1769_1770delinsGA
NM_000314.7:c.1199_1200delinsGA NP_000305.3:p.Ile400Arg
NM_001304717.5:c.1718_1719delinsGA NP_001291646.4:p.Ile573Arg
NM_001304718.2:c.608_609delinsGA NP_001291647.1:p.Ile203Arg
NM_000314.8:c.1199_1200delinsGA MANE Select NP_000305.3:p.Ile400Arg