Canonical Allele Identifier: CA891841630
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965392_87965393delinsGT , CM000672.2:g.87965392_87965393delinsGT GRCh38
NC_000010.10:g.89725149_89725150delinsGT , CM000672.1:g.89725149_89725150delinsGT GRCh37
NC_000010.9:g.89715129_89715130delinsGT NCBI36
NG_007466.2:g.106954_106955delinsGT , LRG_311:g.106954_106955delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1225_1226delinsGT ENSP00000514759.2:p.Arg409Val
ENST00000710265.1:c.*161_*162delinsGT ENSP00000518161.1:n.*161_*162delinsGT
ENST00000688158.2:n.1867_1868delinsGT
ENST00000688922.2:c.*962_*963delinsGT ENSP00000508742.2:n.*962_*963delinsGT
ENST00000700021.1:c.1087_1088delinsGT ENSP00000514757.1:p.Arg363Val
ENST00000700022.1:c.*471_*472delinsGT ENSP00000514758.1:n.*471_*472delinsGT
ENST00000700023.1:n.2290_2291delinsGT
ENST00000700024.1:n.2524_2525delinsGT
ENST00000706954.1:c.1132_1133delinsGT ENSP00000516674.1:p.Arg378Val
ENST00000706955.1:c.*1167_*1168delinsGT ENSP00000516675.1:n.*1167_*1168delinsGT
ENST00000686459.1:c.*718_*719delinsGT ENSP00000508909.1:n.*718_*719delinsGT
ENST00000688158.1:c.*1243_*1244delinsGT ENSP00000509254.1:n.*1243_*1244delinsGT
ENST00000688308.1:c.1132_1133delinsGT ENSP00000508752.1:p.Arg378Val
ENST00000688922.1:c.1053_1054delinsGT
ENST00000693560.1:c.1651_1652delinsGT ENSP00000509861.1:p.Arg551Val
ENST00000371953.8:c.1132_1133delinsGT MANE Select ENSP00000361021.3:p.Arg378Val
ENST00000371953.7:c.1132_1133delinsGT ENSP00000361021.3:p.Arg378Val
NM_000314.5:c.1132_1133delinsGT NP_000305.3:p.Arg378Val
NM_000314.6:c.1132_1133delinsGT NP_000305.3:p.Arg378Val
NM_001304717.2:c.1651_1652delinsGT NP_001291646.2:p.Arg551Val
NM_001304718.1:c.541_542delinsGT NP_001291647.1:p.Arg181Val
XM_006717926.2:c.1087_1088delinsGT XP_006717989.1:p.Arg363Val
XM_011539982.1:c.1036_1037delinsGT XP_011538284.1:p.Arg346Val
XR_945791.1:n.1702_1703delinsGT
NM_000314.7:c.1132_1133delinsGT NP_000305.3:p.Arg378Val
NM_001304717.5:c.1651_1652delinsGT NP_001291646.4:p.Arg551Val
NM_001304718.2:c.541_542delinsGT NP_001291647.1:p.Arg181Val
NM_000314.8:c.1132_1133delinsGT MANE Select NP_000305.3:p.Arg378Val