Canonical Allele Identifier: CA891840877
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957987_87957988delinsCC , CM000672.2:g.87957987_87957988delinsCC GRCh38
NC_000010.10:g.89717744_89717745delinsCC , CM000672.1:g.89717744_89717745delinsCC GRCh37
NC_000010.9:g.89707724_89707725delinsCC NCBI36
NG_007466.2:g.99549_99550delinsCC , LRG_311:g.99549_99550delinsCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.769_770delinsCC ENSP00000514759.2:p.Phe257Pro
ENST00000710265.1:c.769_770delinsCC ENSP00000518161.1:p.Phe257Pro
ENST00000472832.3:c.769_770delinsCC ENSP00000483066.2:p.Phe257Pro
ENST00000688158.2:n.1504_1505delinsCC
ENST00000688922.2:c.*599_*600delinsCC ENSP00000508742.2:n.*599_*600delinsCC
ENST00000700021.1:c.724_725delinsCC ENSP00000514757.1:p.Phe242Pro
ENST00000700022.1:c.*108_*109delinsCC ENSP00000514758.1:n.*108_*109delinsCC
ENST00000700023.1:n.1927_1928delinsCC
ENST00000700024.1:n.2161_2162delinsCC
ENST00000700025.1:n.1538_1539delinsCC
ENST00000700026.1:n.406_407delinsCC
ENST00000700029.1:c.603_604delinsCC
ENST00000706954.1:c.769_770delinsCC ENSP00000516674.1:p.Phe257Pro
ENST00000706955.1:c.*804_*805delinsCC ENSP00000516675.1:n.*804_*805delinsCC
ENST00000686459.1:c.*355_*356delinsCC ENSP00000508909.1:n.*355_*356delinsCC
ENST00000688158.1:c.*880_*881delinsCC ENSP00000509254.1:n.*880_*881delinsCC
ENST00000688308.1:c.769_770delinsCC ENSP00000508752.1:p.Phe257Pro
ENST00000688922.1:c.690_691delinsCC
ENST00000693560.1:c.1288_1289delinsCC ENSP00000509861.1:p.Phe430Pro
ENST00000371953.8:c.769_770delinsCC MANE Select ENSP00000361021.3:p.Phe257Pro
ENST00000371953.7:c.769_770delinsCC ENSP00000361021.3:p.Phe257Pro
ENST00000472832.2:c.196_197delinsCC ENSP00000483066.1:p.Phe66Pro
NM_000314.5:c.769_770delinsCC NP_000305.3:p.Phe257Pro
NM_000314.6:c.769_770delinsCC NP_000305.3:p.Phe257Pro
NM_001304717.2:c.1288_1289delinsCC NP_001291646.2:p.Phe430Pro
NM_001304718.1:c.178_179delinsCC NP_001291647.1:p.Phe60Pro
XM_006717926.2:c.724_725delinsCC XP_006717989.1:p.Phe242Pro
XM_011539981.1:c.769_770delinsCC XP_011538283.1:p.Phe257Pro
XM_011539982.1:c.673_674delinsCC XP_011538284.1:p.Phe225Pro
XR_945791.1:n.1339_1340delinsCC
NM_000314.7:c.769_770delinsCC NP_000305.3:p.Phe257Pro
NM_001304717.5:c.1288_1289delinsCC NP_001291646.4:p.Phe430Pro
NM_001304718.2:c.178_179delinsCC NP_001291647.1:p.Phe60Pro
NM_000314.8:c.769_770delinsCC MANE Select NP_000305.3:p.Phe257Pro