Canonical Allele Identifier: CA2580082295
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 1694040
ClinVar RCV Id: RCV002261909
dbSNP Id: rs2132277361

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957960_87957971del , CM000672.2:g.87957960_87957971del GRCh38
NC_000010.10:g.89717717_89717728del , CM000672.1:g.89717717_89717728del GRCh37
NC_000010.9:g.89707697_89707708del NCBI36
NG_007466.2:g.99522_99533del , LRG_311:g.99522_99533del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.742_753del ENSP00000514759.2:p.Pro248_Gly251del
ENST00000710265.1:c.742_753del ENSP00000518161.1:p.Pro248_Gly251del
ENST00000472832.3:c.742_753del ENSP00000483066.2:p.Pro248_Gly251del
ENST00000688158.2:n.1477_1488del
ENST00000688922.2:c.*572_*583del ENSP00000508742.2:n.*572_*583del
ENST00000700021.1:c.697_708del ENSP00000514757.1:p.Pro233_Gly236del
ENST00000700022.1:c.*81_*92del ENSP00000514758.1:n.*81_*92del
ENST00000700023.1:n.1900_1911del
ENST00000700024.1:n.2134_2145del
ENST00000700025.1:n.1511_1522del
ENST00000700026.1:n.379_390del
ENST00000700029.1:c.576_587del
ENST00000706954.1:c.742_753del ENSP00000516674.1:p.Pro248_Gly251del
ENST00000706955.1:c.*777_*788del ENSP00000516675.1:n.*777_*788del
ENST00000686459.1:c.*328_*339del ENSP00000508909.1:n.*328_*339del
ENST00000688158.1:c.*853_*864del ENSP00000509254.1:n.*853_*864del
ENST00000688308.1:c.742_753del ENSP00000508752.1:p.Pro248_Gly251del
ENST00000688922.1:c.663_674del
ENST00000693560.1:c.1261_1272del ENSP00000509861.1:p.Pro421_Gly424del
ENST00000371953.8:c.742_753del MANE Select ENSP00000361021.3:p.Pro248_Gly251del
ENST00000371953.7:c.742_753del ENSP00000361021.3:p.Pro248_Gly251del
ENST00000472832.2:c.169_180del ENSP00000483066.1:p.Pro57_Gly60del
NM_000314.5:c.742_753del NP_000305.3:p.Pro248_Gly251del
NM_000314.6:c.742_753del NP_000305.3:p.Pro248_Gly251del
NM_001304717.2:c.1261_1272del NP_001291646.2:p.Pro421_Gly424del
NM_001304718.1:c.151_162del NP_001291647.1:p.Pro51_Gly54del
XM_006717926.2:c.697_708del XP_006717989.1:p.Pro233_Gly236del
XM_011539981.1:c.742_753del XP_011538283.1:p.Pro248_Gly251del
XM_011539982.1:c.646_657del XP_011538284.1:p.Pro216_Gly219del
XR_945791.1:n.1312_1323del
NM_000314.7:c.742_753del NP_000305.3:p.Pro248_Gly251del
NM_001304717.5:c.1261_1272del NP_001291646.4:p.Pro421_Gly424del
NM_001304718.2:c.151_162del NP_001291647.1:p.Pro51_Gly54del
NM_000314.8:c.742_753del MANE Select NP_000305.3:p.Pro248_Gly251del