Canonical Allele Identifier: CA891837804
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965392_87965394delinsTTG , CM000672.2:g.87965392_87965394delinsTTG GRCh38
NC_000010.10:g.89725149_89725151delinsTTG , CM000672.1:g.89725149_89725151delinsTTG GRCh37
NC_000010.9:g.89715129_89715131delinsTTG NCBI36
NG_007466.2:g.106954_106956delinsTTG , LRG_311:g.106954_106956delinsTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1225_1227delinsTTG ENSP00000514759.2:p.Arg409Leu
ENST00000710265.1:c.*161_*163delinsTTG ENSP00000518161.1:n.*161_*163delinsTTG
ENST00000688158.2:n.1867_1869delinsTTG
ENST00000688922.2:c.*962_*964delinsTTG ENSP00000508742.2:n.*962_*964delinsTTG
ENST00000700021.1:c.1087_1089delinsTTG ENSP00000514757.1:p.Arg363Leu
ENST00000700022.1:c.*471_*473delinsTTG ENSP00000514758.1:n.*471_*473delinsTTG
ENST00000700023.1:n.2290_2292delinsTTG
ENST00000700024.1:n.2524_2526delinsTTG
ENST00000706954.1:c.1132_1134delinsTTG ENSP00000516674.1:p.Arg378Leu
ENST00000706955.1:c.*1167_*1169delinsTTG ENSP00000516675.1:n.*1167_*1169delinsTTG
ENST00000686459.1:c.*718_*720delinsTTG ENSP00000508909.1:n.*718_*720delinsTTG
ENST00000688158.1:c.*1243_*1245delinsTTG ENSP00000509254.1:n.*1243_*1245delinsTTG
ENST00000688308.1:c.1132_1134delinsTTG ENSP00000508752.1:p.Arg378Leu
ENST00000688922.1:c.1053_1055delinsTTG
ENST00000693560.1:c.1651_1653delinsTTG ENSP00000509861.1:p.Arg551Leu
ENST00000371953.8:c.1132_1134delinsTTG MANE Select ENSP00000361021.3:p.Arg378Leu
ENST00000371953.7:c.1132_1134delinsTTG ENSP00000361021.3:p.Arg378Leu
NM_000314.5:c.1132_1134delinsTTG NP_000305.3:p.Arg378Leu
NM_000314.6:c.1132_1134delinsTTG NP_000305.3:p.Arg378Leu
NM_001304717.2:c.1651_1653delinsTTG NP_001291646.2:p.Arg551Leu
NM_001304718.1:c.541_543delinsTTG NP_001291647.1:p.Arg181Leu
XM_006717926.2:c.1087_1089delinsTTG XP_006717989.1:p.Arg363Leu
XM_011539982.1:c.1036_1038delinsTTG XP_011538284.1:p.Arg346Leu
XR_945791.1:n.1702_1704delinsTTG
NM_000314.7:c.1132_1134delinsTTG NP_000305.3:p.Arg378Leu
NM_001304717.5:c.1651_1653delinsTTG NP_001291646.4:p.Arg551Leu
NM_001304718.2:c.541_543delinsTTG NP_001291647.1:p.Arg181Leu
NM_000314.8:c.1132_1134delinsTTG MANE Select NP_000305.3:p.Arg378Leu