Canonical Allele Identifier: CA891837497
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965359_87965361delinsGAT , CM000672.2:g.87965359_87965361delinsGAT GRCh38
NC_000010.10:g.89725116_89725118delinsGAT , CM000672.1:g.89725116_89725118delinsGAT GRCh37
NC_000010.9:g.89715096_89715098delinsGAT NCBI36
NG_007466.2:g.106921_106923delinsGAT , LRG_311:g.106921_106923delinsGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1192_1194delinsGAT ENSP00000514759.2:p.Pro398Asp
ENST00000710265.1:c.*128_*130delinsGAT ENSP00000518161.1:n.*128_*130delinsGAT
ENST00000688158.2:n.1834_1836delinsGAT
ENST00000688922.2:c.*929_*931delinsGAT ENSP00000508742.2:n.*929_*931delinsGAT
ENST00000700021.1:c.1054_1056delinsGAT ENSP00000514757.1:p.Pro352Asp
ENST00000700022.1:c.*438_*440delinsGAT ENSP00000514758.1:n.*438_*440delinsGAT
ENST00000700023.1:n.2257_2259delinsGAT
ENST00000700024.1:n.2491_2493delinsGAT
ENST00000706954.1:c.1099_1101delinsGAT ENSP00000516674.1:p.Pro367Asp
ENST00000706955.1:c.*1134_*1136delinsGAT ENSP00000516675.1:n.*1134_*1136delinsGAT
ENST00000686459.1:c.*685_*687delinsGAT ENSP00000508909.1:n.*685_*687delinsGAT
ENST00000688158.1:c.*1210_*1212delinsGAT ENSP00000509254.1:n.*1210_*1212delinsGAT
ENST00000688308.1:c.1099_1101delinsGAT ENSP00000508752.1:p.Pro367Asp
ENST00000688922.1:c.1020_1022delinsGAT
ENST00000693560.1:c.1618_1620delinsGAT ENSP00000509861.1:p.Pro540Asp
ENST00000371953.8:c.1099_1101delinsGAT MANE Select ENSP00000361021.3:p.Pro367Asp
ENST00000371953.7:c.1099_1101delinsGAT ENSP00000361021.3:p.Pro367Asp
NM_000314.5:c.1099_1101delinsGAT NP_000305.3:p.Pro367Asp
NM_000314.6:c.1099_1101delinsGAT NP_000305.3:p.Pro367Asp
NM_001304717.2:c.1618_1620delinsGAT NP_001291646.2:p.Pro540Asp
NM_001304718.1:c.508_510delinsGAT NP_001291647.1:p.Pro170Asp
XM_006717926.2:c.1054_1056delinsGAT XP_006717989.1:p.Pro352Asp
XM_011539982.1:c.1003_1005delinsGAT XP_011538284.1:p.Pro335Asp
XR_945791.1:n.1669_1671delinsGAT
NM_000314.7:c.1099_1101delinsGAT NP_000305.3:p.Pro367Asp
NM_001304717.5:c.1618_1620delinsGAT NP_001291646.4:p.Pro540Asp
NM_001304718.2:c.508_510delinsGAT NP_001291647.1:p.Pro170Asp
NM_000314.8:c.1099_1101delinsGAT MANE Select NP_000305.3:p.Pro367Asp