Canonical Allele Identifier: CA891837806
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965392_87965394delinsGTT , CM000672.2:g.87965392_87965394delinsGTT GRCh38
NC_000010.10:g.89725149_89725151delinsGTT , CM000672.1:g.89725149_89725151delinsGTT GRCh37
NC_000010.9:g.89715129_89715131delinsGTT NCBI36
NG_007466.2:g.106954_106956delinsGTT , LRG_311:g.106954_106956delinsGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1225_1227delinsGTT ENSP00000514759.2:p.Arg409Val
ENST00000710265.1:c.*161_*163delinsGTT ENSP00000518161.1:n.*161_*163delinsGTT
ENST00000688158.2:n.1867_1869delinsGTT
ENST00000688922.2:c.*962_*964delinsGTT ENSP00000508742.2:n.*962_*964delinsGTT
ENST00000700021.1:c.1087_1089delinsGTT ENSP00000514757.1:p.Arg363Val
ENST00000700022.1:c.*471_*473delinsGTT ENSP00000514758.1:n.*471_*473delinsGTT
ENST00000700023.1:n.2290_2292delinsGTT
ENST00000700024.1:n.2524_2526delinsGTT
ENST00000706954.1:c.1132_1134delinsGTT ENSP00000516674.1:p.Arg378Val
ENST00000706955.1:c.*1167_*1169delinsGTT ENSP00000516675.1:n.*1167_*1169delinsGTT
ENST00000686459.1:c.*718_*720delinsGTT ENSP00000508909.1:n.*718_*720delinsGTT
ENST00000688158.1:c.*1243_*1245delinsGTT ENSP00000509254.1:n.*1243_*1245delinsGTT
ENST00000688308.1:c.1132_1134delinsGTT ENSP00000508752.1:p.Arg378Val
ENST00000688922.1:c.1053_1055delinsGTT
ENST00000693560.1:c.1651_1653delinsGTT ENSP00000509861.1:p.Arg551Val
ENST00000371953.8:c.1132_1134delinsGTT MANE Select ENSP00000361021.3:p.Arg378Val
ENST00000371953.7:c.1132_1134delinsGTT ENSP00000361021.3:p.Arg378Val
NM_000314.5:c.1132_1134delinsGTT NP_000305.3:p.Arg378Val
NM_000314.6:c.1132_1134delinsGTT NP_000305.3:p.Arg378Val
NM_001304717.2:c.1651_1653delinsGTT NP_001291646.2:p.Arg551Val
NM_001304718.1:c.541_543delinsGTT NP_001291647.1:p.Arg181Val
XM_006717926.2:c.1087_1089delinsGTT XP_006717989.1:p.Arg363Val
XM_011539982.1:c.1036_1038delinsGTT XP_011538284.1:p.Arg346Val
XR_945791.1:n.1702_1704delinsGTT
NM_000314.7:c.1132_1134delinsGTT NP_000305.3:p.Arg378Val
NM_001304717.5:c.1651_1653delinsGTT NP_001291646.4:p.Arg551Val
NM_001304718.2:c.541_543delinsGTT NP_001291647.1:p.Arg181Val
NM_000314.8:c.1132_1134delinsGTT MANE Select NP_000305.3:p.Arg378Val