Canonical Allele Identifier: CA891838087
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965432_87965433delinsAA , CM000672.2:g.87965432_87965433delinsAA GRCh38
NC_000010.10:g.89725189_89725190delinsAA , CM000672.1:g.89725189_89725190delinsAA GRCh37
NC_000010.9:g.89715169_89715170delinsAA NCBI36
NG_007466.2:g.106994_106995delinsAA , LRG_311:g.106994_106995delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1265_1266delinsAA ENSP00000514759.2:p.Pro422Gln
ENST00000710265.1:c.*201_*202delinsAA ENSP00000518161.1:n.*201_*202delinsAA
ENST00000688158.2:n.1907_1908delinsAA
ENST00000688922.2:c.*1002_*1003delinsAA ENSP00000508742.2:n.*1002_*1003delinsAA
ENST00000700021.1:c.1127_1128delinsAA ENSP00000514757.1:p.Pro376Gln
ENST00000700022.1:c.*511_*512delinsAA ENSP00000514758.1:n.*511_*512delinsAA
ENST00000700023.1:n.2330_2331delinsAA
ENST00000700024.1:n.2564_2565delinsAA
ENST00000706954.1:c.1172_1173delinsAA ENSP00000516674.1:p.Pro391Gln
ENST00000706955.1:c.*1207_*1208delinsAA ENSP00000516675.1:n.*1207_*1208delinsAA
ENST00000686459.1:c.*758_*759delinsAA ENSP00000508909.1:n.*758_*759delinsAA
ENST00000688158.1:c.*1283_*1284delinsAA ENSP00000509254.1:n.*1283_*1284delinsAA
ENST00000688308.1:c.1172_1173delinsAA ENSP00000508752.1:p.Pro391Gln
ENST00000688922.1:c.1093_1094delinsAA
ENST00000693560.1:c.1691_1692delinsAA ENSP00000509861.1:p.Pro564Gln
ENST00000371953.8:c.1172_1173delinsAA MANE Select ENSP00000361021.3:p.Pro391Gln
ENST00000371953.7:c.1172_1173delinsAA ENSP00000361021.3:p.Pro391Gln
NM_000314.5:c.1172_1173delinsAA NP_000305.3:p.Pro391Gln
NM_000314.6:c.1172_1173delinsAA NP_000305.3:p.Pro391Gln
NM_001304717.2:c.1691_1692delinsAA NP_001291646.2:p.Pro564Gln
NM_001304718.1:c.581_582delinsAA NP_001291647.1:p.Pro194Gln
XM_006717926.2:c.1127_1128delinsAA XP_006717989.1:p.Pro376Gln
XM_011539982.1:c.1076_1077delinsAA XP_011538284.1:p.Pro359Gln
XR_945791.1:n.1742_1743delinsAA
NM_000314.7:c.1172_1173delinsAA NP_000305.3:p.Pro391Gln
NM_001304717.5:c.1691_1692delinsAA NP_001291646.4:p.Pro564Gln
NM_001304718.2:c.581_582delinsAA NP_001291647.1:p.Pro194Gln
NM_000314.8:c.1172_1173delinsAA MANE Select NP_000305.3:p.Pro391Gln