Canonical Allele Identifier: CA1926173092
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs1860730518

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965234_87965236del , CM000672.2:g.87965234_87965236del GRCh38
NC_000010.10:g.89724991_89724993del , CM000672.1:g.89724991_89724993del GRCh37
NC_000010.9:g.89714971_89714973del NCBI36
NG_007466.2:g.106796_106798del , LRG_311:g.106796_106798del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1120-53_1120-51del ENSP00000514759.2:n.1120-53_1120-51del
ENST00000710265.1:c.*56-53_*56-51del ENSP00000518161.1:n.*56-53_*56-51del
ENST00000688158.2:n.1762-53_1762-51del
ENST00000688922.2:c.*857-53_*857-51del ENSP00000508742.2:n.*857-53_*857-51del
ENST00000700021.1:c.982-53_982-51del ENSP00000514757.1:n.982-53_982-51del
ENST00000700022.1:c.*366-53_*366-51del ENSP00000514758.1:n.*366-53_*366-51del
ENST00000700023.1:n.2185-53_2185-51del
ENST00000700024.1:n.2419-53_2419-51del
ENST00000706954.1:c.1027-53_1027-51del ENSP00000516674.1:n.1027-53_1027-51del
ENST00000706955.1:c.*1062-53_*1062-51del ENSP00000516675.1:n.*1062-53_*1062-51del
ENST00000686459.1:c.*613-53_*613-51del ENSP00000508909.1:n.*613-53_*613-51del
ENST00000688158.1:c.*1138-53_*1138-51del ENSP00000509254.1:n.*1138-53_*1138-51del
ENST00000688308.1:c.1027-53_1027-51del ENSP00000508752.1:n.1027-53_1027-51del
ENST00000688922.1:c.948-53_948-51del
ENST00000693560.1:c.1546-53_1546-51del ENSP00000509861.1:n.1546-53_1546-51del
ENST00000371953.8:c.1027-53_1027-51del MANE Select ENSP00000361021.3:n.1027-53_1027-51del
ENST00000371953.7:c.1027-53_1027-51del ENSP00000361021.3:n.1027-53_1027-51del
NM_000314.5:c.1027-53_1027-51del NP_000305.3:n.1027-53_1027-51del
NM_000314.6:c.1027-53_1027-51del NP_000305.3:n.1027-53_1027-51del
NM_001304717.2:c.1546-53_1546-51del NP_001291646.2:n.1546-53_1546-51del
NM_001304718.1:c.436-53_436-51del NP_001291647.1:n.436-53_436-51del
XM_006717926.2:c.982-53_982-51del XP_006717989.1:n.982-53_982-51del
XM_011539982.1:c.931-53_931-51del XP_011538284.1:n.931-53_931-51del
XR_945791.1:n.1597-53_1597-51del
NM_000314.7:c.1027-53_1027-51del NP_000305.3:n.1027-53_1027-51del
NM_001304717.5:c.1546-53_1546-51del NP_001291646.4:n.1546-53_1546-51del
NM_001304718.2:c.436-53_436-51del NP_001291647.1:n.436-53_436-51del
NM_000314.8:c.1027-53_1027-51del MANE Select NP_000305.3:n.1027-53_1027-51del