Canonical Allele Identifier: CA891837910
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965407_87965408delinsGA , CM000672.2:g.87965407_87965408delinsGA GRCh38
NC_000010.10:g.89725164_89725165delinsGA , CM000672.1:g.89725164_89725165delinsGA GRCh37
NC_000010.9:g.89715144_89715145delinsGA NCBI36
NG_007466.2:g.106969_106970delinsGA , LRG_311:g.106969_106970delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1240_1241delinsGA ENSP00000514759.2:p.Thr414Asp
ENST00000710265.1:c.*176_*177delinsGA ENSP00000518161.1:n.*176_*177delinsGA
ENST00000688158.2:n.1882_1883delinsGA
ENST00000688922.2:c.*977_*978delinsGA ENSP00000508742.2:n.*977_*978delinsGA
ENST00000700021.1:c.1102_1103delinsGA ENSP00000514757.1:p.Thr368Asp
ENST00000700022.1:c.*486_*487delinsGA ENSP00000514758.1:n.*486_*487delinsGA
ENST00000700023.1:n.2305_2306delinsGA
ENST00000700024.1:n.2539_2540delinsGA
ENST00000706954.1:c.1147_1148delinsGA ENSP00000516674.1:p.Thr383Asp
ENST00000706955.1:c.*1182_*1183delinsGA ENSP00000516675.1:n.*1182_*1183delinsGA
ENST00000686459.1:c.*733_*734delinsGA ENSP00000508909.1:n.*733_*734delinsGA
ENST00000688158.1:c.*1258_*1259delinsGA ENSP00000509254.1:n.*1258_*1259delinsGA
ENST00000688308.1:c.1147_1148delinsGA ENSP00000508752.1:p.Thr383Asp
ENST00000688922.1:c.1068_1069delinsGA
ENST00000693560.1:c.1666_1667delinsGA ENSP00000509861.1:p.Thr556Asp
ENST00000371953.8:c.1147_1148delinsGA MANE Select ENSP00000361021.3:p.Thr383Asp
ENST00000371953.7:c.1147_1148delinsGA ENSP00000361021.3:p.Thr383Asp
NM_000314.5:c.1147_1148delinsGA NP_000305.3:p.Thr383Asp
NM_000314.6:c.1147_1148delinsGA NP_000305.3:p.Thr383Asp
NM_001304717.2:c.1666_1667delinsGA NP_001291646.2:p.Thr556Asp
NM_001304718.1:c.556_557delinsGA NP_001291647.1:p.Thr186Asp
XM_006717926.2:c.1102_1103delinsGA XP_006717989.1:p.Thr368Asp
XM_011539982.1:c.1051_1052delinsGA XP_011538284.1:p.Thr351Asp
XR_945791.1:n.1717_1718delinsGA
NM_000314.7:c.1147_1148delinsGA NP_000305.3:p.Thr383Asp
NM_001304717.5:c.1666_1667delinsGA NP_001291646.4:p.Thr556Asp
NM_001304718.2:c.556_557delinsGA NP_001291647.1:p.Thr186Asp
NM_000314.8:c.1147_1148delinsGA MANE Select NP_000305.3:p.Thr383Asp