Canonical Allele Identifier: CA891837419
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965347_87965348delinsGG , CM000672.2:g.87965347_87965348delinsGG GRCh38
NC_000010.10:g.89725104_89725105delinsGG , CM000672.1:g.89725104_89725105delinsGG GRCh37
NC_000010.9:g.89715084_89715085delinsGG NCBI36
NG_007466.2:g.106909_106910delinsGG , LRG_311:g.106909_106910delinsGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1180_1181delinsGG ENSP00000514759.2:p.Thr394Gly
ENST00000710265.1:c.*116_*117delinsGG ENSP00000518161.1:n.*116_*117delinsGG
ENST00000688158.2:n.1822_1823delinsGG
ENST00000688922.2:c.*917_*918delinsGG ENSP00000508742.2:n.*917_*918delinsGG
ENST00000700021.1:c.1042_1043delinsGG ENSP00000514757.1:p.Thr348Gly
ENST00000700022.1:c.*426_*427delinsGG ENSP00000514758.1:n.*426_*427delinsGG
ENST00000700023.1:n.2245_2246delinsGG
ENST00000700024.1:n.2479_2480delinsGG
ENST00000706954.1:c.1087_1088delinsGG ENSP00000516674.1:p.Thr363Gly
ENST00000706955.1:c.*1122_*1123delinsGG ENSP00000516675.1:n.*1122_*1123delinsGG
ENST00000686459.1:c.*673_*674delinsGG ENSP00000508909.1:n.*673_*674delinsGG
ENST00000688158.1:c.*1198_*1199delinsGG ENSP00000509254.1:n.*1198_*1199delinsGG
ENST00000688308.1:c.1087_1088delinsGG ENSP00000508752.1:p.Thr363Gly
ENST00000688922.1:c.1008_1009delinsGG
ENST00000693560.1:c.1606_1607delinsGG ENSP00000509861.1:p.Thr536Gly
ENST00000371953.8:c.1087_1088delinsGG MANE Select ENSP00000361021.3:p.Thr363Gly
ENST00000371953.7:c.1087_1088delinsGG ENSP00000361021.3:p.Thr363Gly
NM_000314.5:c.1087_1088delinsGG NP_000305.3:p.Thr363Gly
NM_000314.6:c.1087_1088delinsGG NP_000305.3:p.Thr363Gly
NM_001304717.2:c.1606_1607delinsGG NP_001291646.2:p.Thr536Gly
NM_001304718.1:c.496_497delinsGG NP_001291647.1:p.Thr166Gly
XM_006717926.2:c.1042_1043delinsGG XP_006717989.1:p.Thr348Gly
XM_011539982.1:c.991_992delinsGG XP_011538284.1:p.Thr331Gly
XR_945791.1:n.1657_1658delinsGG
NM_000314.7:c.1087_1088delinsGG NP_000305.3:p.Thr363Gly
NM_001304717.5:c.1606_1607delinsGG NP_001291646.4:p.Thr536Gly
NM_001304718.2:c.496_497delinsGG NP_001291647.1:p.Thr166Gly
NM_000314.8:c.1087_1088delinsGG MANE Select NP_000305.3:p.Thr363Gly