Canonical Allele Identifier: CA891840881
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957987_87957988delinsGG , CM000672.2:g.87957987_87957988delinsGG GRCh38
NC_000010.10:g.89717744_89717745delinsGG , CM000672.1:g.89717744_89717745delinsGG GRCh37
NC_000010.9:g.89707724_89707725delinsGG NCBI36
NG_007466.2:g.99549_99550delinsGG , LRG_311:g.99549_99550delinsGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.769_770delinsGG ENSP00000514759.2:p.Phe257Gly
ENST00000710265.1:c.769_770delinsGG ENSP00000518161.1:p.Phe257Gly
ENST00000472832.3:c.769_770delinsGG ENSP00000483066.2:p.Phe257Gly
ENST00000688158.2:n.1504_1505delinsGG
ENST00000688922.2:c.*599_*600delinsGG ENSP00000508742.2:n.*599_*600delinsGG
ENST00000700021.1:c.724_725delinsGG ENSP00000514757.1:p.Phe242Gly
ENST00000700022.1:c.*108_*109delinsGG ENSP00000514758.1:n.*108_*109delinsGG
ENST00000700023.1:n.1927_1928delinsGG
ENST00000700024.1:n.2161_2162delinsGG
ENST00000700025.1:n.1538_1539delinsGG
ENST00000700026.1:n.406_407delinsGG
ENST00000700029.1:c.603_604delinsGG
ENST00000706954.1:c.769_770delinsGG ENSP00000516674.1:p.Phe257Gly
ENST00000706955.1:c.*804_*805delinsGG ENSP00000516675.1:n.*804_*805delinsGG
ENST00000686459.1:c.*355_*356delinsGG ENSP00000508909.1:n.*355_*356delinsGG
ENST00000688158.1:c.*880_*881delinsGG ENSP00000509254.1:n.*880_*881delinsGG
ENST00000688308.1:c.769_770delinsGG ENSP00000508752.1:p.Phe257Gly
ENST00000688922.1:c.690_691delinsGG
ENST00000693560.1:c.1288_1289delinsGG ENSP00000509861.1:p.Phe430Gly
ENST00000371953.8:c.769_770delinsGG MANE Select ENSP00000361021.3:p.Phe257Gly
ENST00000371953.7:c.769_770delinsGG ENSP00000361021.3:p.Phe257Gly
ENST00000472832.2:c.196_197delinsGG ENSP00000483066.1:p.Phe66Gly
NM_000314.5:c.769_770delinsGG NP_000305.3:p.Phe257Gly
NM_000314.6:c.769_770delinsGG NP_000305.3:p.Phe257Gly
NM_001304717.2:c.1288_1289delinsGG NP_001291646.2:p.Phe430Gly
NM_001304718.1:c.178_179delinsGG NP_001291647.1:p.Phe60Gly
XM_006717926.2:c.724_725delinsGG XP_006717989.1:p.Phe242Gly
XM_011539981.1:c.769_770delinsGG XP_011538283.1:p.Phe257Gly
XM_011539982.1:c.673_674delinsGG XP_011538284.1:p.Phe225Gly
XR_945791.1:n.1339_1340delinsGG
NM_000314.7:c.769_770delinsGG NP_000305.3:p.Phe257Gly
NM_001304717.5:c.1288_1289delinsGG NP_001291646.4:p.Phe430Gly
NM_001304718.2:c.178_179delinsGG NP_001291647.1:p.Phe60Gly
NM_000314.8:c.769_770delinsGG MANE Select NP_000305.3:p.Phe257Gly