Canonical Allele Identifier: CA2722451823
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs2132288847

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965209_87965210del , CM000672.2:g.87965209_87965210del GRCh38
NC_000010.10:g.89724966_89724967del , CM000672.1:g.89724966_89724967del GRCh37
NC_000010.9:g.89714946_89714947del NCBI36
NG_007466.2:g.106771_106772del , LRG_311:g.106771_106772del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1120-78_1120-77del ENSP00000514759.2:n.1120-78_1120-77del
ENST00000710265.1:c.*56-78_*56-77del ENSP00000518161.1:n.*56-78_*56-77del
ENST00000688158.2:n.1762-78_1762-77del
ENST00000688922.2:c.*857-78_*857-77del ENSP00000508742.2:n.*857-78_*857-77del
ENST00000700021.1:c.982-78_982-77del ENSP00000514757.1:n.982-78_982-77del
ENST00000700022.1:c.*366-78_*366-77del ENSP00000514758.1:n.*366-78_*366-77del
ENST00000700023.1:n.2185-78_2185-77del
ENST00000700024.1:n.2419-78_2419-77del
ENST00000706954.1:c.1027-78_1027-77del ENSP00000516674.1:n.1027-78_1027-77del
ENST00000706955.1:c.*1062-78_*1062-77del ENSP00000516675.1:n.*1062-78_*1062-77del
ENST00000686459.1:c.*613-78_*613-77del ENSP00000508909.1:n.*613-78_*613-77del
ENST00000688158.1:c.*1138-78_*1138-77del ENSP00000509254.1:n.*1138-78_*1138-77del
ENST00000688308.1:c.1027-78_1027-77del ENSP00000508752.1:n.1027-78_1027-77del
ENST00000688922.1:c.948-78_948-77del
ENST00000693560.1:c.1546-78_1546-77del ENSP00000509861.1:n.1546-78_1546-77del
ENST00000371953.8:c.1027-78_1027-77del MANE Select ENSP00000361021.3:n.1027-78_1027-77del
ENST00000371953.7:c.1027-78_1027-77del ENSP00000361021.3:n.1027-78_1027-77del
NM_000314.5:c.1027-78_1027-77del NP_000305.3:n.1027-78_1027-77del
NM_000314.6:c.1027-78_1027-77del NP_000305.3:n.1027-78_1027-77del
NM_001304717.2:c.1546-78_1546-77del NP_001291646.2:n.1546-78_1546-77del
NM_001304718.1:c.436-78_436-77del NP_001291647.1:n.436-78_436-77del
XM_006717926.2:c.982-78_982-77del XP_006717989.1:n.982-78_982-77del
XM_011539982.1:c.931-78_931-77del XP_011538284.1:n.931-78_931-77del
XR_945791.1:n.1597-78_1597-77del
NM_000314.7:c.1027-78_1027-77del NP_000305.3:n.1027-78_1027-77del
NM_001304717.5:c.1546-78_1546-77del NP_001291646.4:n.1546-78_1546-77del
NM_001304718.2:c.436-78_436-77del NP_001291647.1:n.436-78_436-77del
NM_000314.8:c.1027-78_1027-77del MANE Select NP_000305.3:n.1027-78_1027-77del