Canonical Allele Identifier: CA891837793
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965392_87965393delinsCC , CM000672.2:g.87965392_87965393delinsCC GRCh38
NC_000010.10:g.89725149_89725150delinsCC , CM000672.1:g.89725149_89725150delinsCC GRCh37
NC_000010.9:g.89715129_89715130delinsCC NCBI36
NG_007466.2:g.106954_106955delinsCC , LRG_311:g.106954_106955delinsCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1225_1226delinsCC ENSP00000514759.2:p.Arg409Pro
ENST00000710265.1:c.*161_*162delinsCC ENSP00000518161.1:n.*161_*162delinsCC
ENST00000688158.2:n.1867_1868delinsCC
ENST00000688922.2:c.*962_*963delinsCC ENSP00000508742.2:n.*962_*963delinsCC
ENST00000700021.1:c.1087_1088delinsCC ENSP00000514757.1:p.Arg363Pro
ENST00000700022.1:c.*471_*472delinsCC ENSP00000514758.1:n.*471_*472delinsCC
ENST00000700023.1:n.2290_2291delinsCC
ENST00000700024.1:n.2524_2525delinsCC
ENST00000706954.1:c.1132_1133delinsCC ENSP00000516674.1:p.Arg378Pro
ENST00000706955.1:c.*1167_*1168delinsCC ENSP00000516675.1:n.*1167_*1168delinsCC
ENST00000686459.1:c.*718_*719delinsCC ENSP00000508909.1:n.*718_*719delinsCC
ENST00000688158.1:c.*1243_*1244delinsCC ENSP00000509254.1:n.*1243_*1244delinsCC
ENST00000688308.1:c.1132_1133delinsCC ENSP00000508752.1:p.Arg378Pro
ENST00000688922.1:c.1053_1054delinsCC
ENST00000693560.1:c.1651_1652delinsCC ENSP00000509861.1:p.Arg551Pro
ENST00000371953.8:c.1132_1133delinsCC MANE Select ENSP00000361021.3:p.Arg378Pro
ENST00000371953.7:c.1132_1133delinsCC ENSP00000361021.3:p.Arg378Pro
NM_000314.5:c.1132_1133delinsCC NP_000305.3:p.Arg378Pro
NM_000314.6:c.1132_1133delinsCC NP_000305.3:p.Arg378Pro
NM_001304717.2:c.1651_1652delinsCC NP_001291646.2:p.Arg551Pro
NM_001304718.1:c.541_542delinsCC NP_001291647.1:p.Arg181Pro
XM_006717926.2:c.1087_1088delinsCC XP_006717989.1:p.Arg363Pro
XM_011539982.1:c.1036_1037delinsCC XP_011538284.1:p.Arg346Pro
XR_945791.1:n.1702_1703delinsCC
NM_000314.7:c.1132_1133delinsCC NP_000305.3:p.Arg378Pro
NM_001304717.5:c.1651_1652delinsCC NP_001291646.4:p.Arg551Pro
NM_001304718.2:c.541_542delinsCC NP_001291647.1:p.Arg181Pro
NM_000314.8:c.1132_1133delinsCC MANE Select NP_000305.3:p.Arg378Pro