Canonical Allele Identifier: CA891837805
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965392_87965393delinsTA , CM000672.2:g.87965392_87965393delinsTA GRCh38
NC_000010.10:g.89725149_89725150delinsTA , CM000672.1:g.89725149_89725150delinsTA GRCh37
NC_000010.9:g.89715129_89715130delinsTA NCBI36
NG_007466.2:g.106954_106955delinsTA , LRG_311:g.106954_106955delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1225_1226delinsTA ENSP00000514759.2:p.Arg409Ter
ENST00000710265.1:c.*161_*162delinsTA ENSP00000518161.1:n.*161_*162delinsTA
ENST00000688158.2:n.1867_1868delinsTA
ENST00000688922.2:c.*962_*963delinsTA ENSP00000508742.2:n.*962_*963delinsTA
ENST00000700021.1:c.1087_1088delinsTA ENSP00000514757.1:p.Arg363Ter
ENST00000700022.1:c.*471_*472delinsTA ENSP00000514758.1:n.*471_*472delinsTA
ENST00000700023.1:n.2290_2291delinsTA
ENST00000700024.1:n.2524_2525delinsTA
ENST00000706954.1:c.1132_1133delinsTA ENSP00000516674.1:p.Arg378Ter
ENST00000706955.1:c.*1167_*1168delinsTA ENSP00000516675.1:n.*1167_*1168delinsTA
ENST00000686459.1:c.*718_*719delinsTA ENSP00000508909.1:n.*718_*719delinsTA
ENST00000688158.1:c.*1243_*1244delinsTA ENSP00000509254.1:n.*1243_*1244delinsTA
ENST00000688308.1:c.1132_1133delinsTA ENSP00000508752.1:p.Arg378Ter
ENST00000688922.1:c.1053_1054delinsTA
ENST00000693560.1:c.1651_1652delinsTA ENSP00000509861.1:p.Arg551Ter
ENST00000371953.8:c.1132_1133delinsTA MANE Select ENSP00000361021.3:p.Arg378Ter
ENST00000371953.7:c.1132_1133delinsTA ENSP00000361021.3:p.Arg378Ter
NM_000314.5:c.1132_1133delinsTA NP_000305.3:p.Arg378Ter
NM_000314.6:c.1132_1133delinsTA NP_000305.3:p.Arg378Ter
NM_001304717.2:c.1651_1652delinsTA NP_001291646.2:p.Arg551Ter
NM_001304718.1:c.541_542delinsTA NP_001291647.1:p.Arg181Ter
XM_006717926.2:c.1087_1088delinsTA XP_006717989.1:p.Arg363Ter
XM_011539982.1:c.1036_1037delinsTA XP_011538284.1:p.Arg346Ter
XR_945791.1:n.1702_1703delinsTA
NM_000314.7:c.1132_1133delinsTA NP_000305.3:p.Arg378Ter
NM_001304717.5:c.1651_1652delinsTA NP_001291646.4:p.Arg551Ter
NM_001304718.2:c.541_542delinsTA NP_001291647.1:p.Arg181Ter
NM_000314.8:c.1132_1133delinsTA MANE Select NP_000305.3:p.Arg378Ter