Canonical Allele Identifier: CA2695202683
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957959_87957964del , CM000672.2:g.87957959_87957964del GRCh38
NC_000010.10:g.89717716_89717721del , CM000672.1:g.89717716_89717721del GRCh37
NC_000010.9:g.89707696_89707701del NCBI36
NG_007466.2:g.99521_99526del , LRG_311:g.99521_99526del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.741_746del ENSP00000514759.2:p.Pro248_Val249del
ENST00000710265.1:c.741_746del ENSP00000518161.1:p.Pro248_Val249del
ENST00000472832.3:c.741_746del ENSP00000483066.2:p.Pro248_Val249del
ENST00000688158.2:n.1476_1481del
ENST00000688922.2:c.*571_*576del ENSP00000508742.2:n.*571_*576del
ENST00000700021.1:c.696_701del ENSP00000514757.1:p.Pro233_Val234del
ENST00000700022.1:c.*80_*85del ENSP00000514758.1:n.*80_*85del
ENST00000700023.1:n.1899_1904del
ENST00000700024.1:n.2133_2138del
ENST00000700025.1:n.1510_1515del
ENST00000700026.1:n.378_383del
ENST00000700029.1:c.575_580del
ENST00000706954.1:c.741_746del ENSP00000516674.1:p.Pro248_Val249del
ENST00000706955.1:c.*776_*781del ENSP00000516675.1:n.*776_*781del
ENST00000686459.1:c.*327_*332del ENSP00000508909.1:n.*327_*332del
ENST00000688158.1:c.*852_*857del ENSP00000509254.1:n.*852_*857del
ENST00000688308.1:c.741_746del ENSP00000508752.1:p.Pro248_Val249del
ENST00000688922.1:c.662_667del
ENST00000693560.1:c.1260_1265del ENSP00000509861.1:p.Pro421_Val422del
ENST00000371953.8:c.741_746del MANE Select ENSP00000361021.3:p.Pro248_Val249del
ENST00000371953.7:c.741_746del ENSP00000361021.3:p.Pro248_Val249del
ENST00000472832.2:c.168_173del ENSP00000483066.1:p.Pro57_Val58del
NM_000314.5:c.741_746del NP_000305.3:p.Pro248_Val249del
NM_000314.6:c.741_746del NP_000305.3:p.Pro248_Val249del
NM_001304717.2:c.1260_1265del NP_001291646.2:p.Pro421_Val422del
NM_001304718.1:c.150_155del NP_001291647.1:p.Pro51_Val52del
XM_006717926.2:c.696_701del XP_006717989.1:p.Pro233_Val234del
XM_011539981.1:c.741_746del XP_011538283.1:p.Pro248_Val249del
XM_011539982.1:c.645_650del XP_011538284.1:p.Pro216_Val217del
XR_945791.1:n.1311_1316del
NM_000314.7:c.741_746del NP_000305.3:p.Pro248_Val249del
NM_001304717.5:c.1260_1265del NP_001291646.4:p.Pro421_Val422del
NM_001304718.2:c.150_155del NP_001291647.1:p.Pro51_Val52del
NM_000314.8:c.741_746del MANE Select NP_000305.3:p.Pro248_Val249del