Canonical Allele Identifier: CA891837801
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965392_87965394delinsTAT , CM000672.2:g.87965392_87965394delinsTAT GRCh38
NC_000010.10:g.89725149_89725151delinsTAT , CM000672.1:g.89725149_89725151delinsTAT GRCh37
NC_000010.9:g.89715129_89715131delinsTAT NCBI36
NG_007466.2:g.106954_106956delinsTAT , LRG_311:g.106954_106956delinsTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1225_1227delinsTAT ENSP00000514759.2:p.Arg409Tyr
ENST00000710265.1:c.*161_*163delinsTAT ENSP00000518161.1:n.*161_*163delinsTAT
ENST00000688158.2:n.1867_1869delinsTAT
ENST00000688922.2:c.*962_*964delinsTAT ENSP00000508742.2:n.*962_*964delinsTAT
ENST00000700021.1:c.1087_1089delinsTAT ENSP00000514757.1:p.Arg363Tyr
ENST00000700022.1:c.*471_*473delinsTAT ENSP00000514758.1:n.*471_*473delinsTAT
ENST00000700023.1:n.2290_2292delinsTAT
ENST00000700024.1:n.2524_2526delinsTAT
ENST00000706954.1:c.1132_1134delinsTAT ENSP00000516674.1:p.Arg378Tyr
ENST00000706955.1:c.*1167_*1169delinsTAT ENSP00000516675.1:n.*1167_*1169delinsTAT
ENST00000686459.1:c.*718_*720delinsTAT ENSP00000508909.1:n.*718_*720delinsTAT
ENST00000688158.1:c.*1243_*1245delinsTAT ENSP00000509254.1:n.*1243_*1245delinsTAT
ENST00000688308.1:c.1132_1134delinsTAT ENSP00000508752.1:p.Arg378Tyr
ENST00000688922.1:c.1053_1055delinsTAT
ENST00000693560.1:c.1651_1653delinsTAT ENSP00000509861.1:p.Arg551Tyr
ENST00000371953.8:c.1132_1134delinsTAT MANE Select ENSP00000361021.3:p.Arg378Tyr
ENST00000371953.7:c.1132_1134delinsTAT ENSP00000361021.3:p.Arg378Tyr
NM_000314.5:c.1132_1134delinsTAT NP_000305.3:p.Arg378Tyr
NM_000314.6:c.1132_1134delinsTAT NP_000305.3:p.Arg378Tyr
NM_001304717.2:c.1651_1653delinsTAT NP_001291646.2:p.Arg551Tyr
NM_001304718.1:c.541_543delinsTAT NP_001291647.1:p.Arg181Tyr
XM_006717926.2:c.1087_1089delinsTAT XP_006717989.1:p.Arg363Tyr
XM_011539982.1:c.1036_1038delinsTAT XP_011538284.1:p.Arg346Tyr
XR_945791.1:n.1702_1704delinsTAT
NM_000314.7:c.1132_1134delinsTAT NP_000305.3:p.Arg378Tyr
NM_001304717.5:c.1651_1653delinsTAT NP_001291646.4:p.Arg551Tyr
NM_001304718.2:c.541_543delinsTAT NP_001291647.1:p.Arg181Tyr
NM_000314.8:c.1132_1134delinsTAT MANE Select NP_000305.3:p.Arg378Tyr