Canonical Allele Identifier: CA891839988
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957988_87957989delinsGT , CM000672.2:g.87957988_87957989delinsGT GRCh38
NC_000010.10:g.89717745_89717746delinsGT , CM000672.1:g.89717745_89717746delinsGT GRCh37
NC_000010.9:g.89707725_89707726delinsGT NCBI36
NG_007466.2:g.99550_99551delinsGT , LRG_311:g.99550_99551delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.770_771delinsGT ENSP00000514759.2:p.Phe257Cys
ENST00000710265.1:c.770_771delinsGT ENSP00000518161.1:p.Phe257Cys
ENST00000472832.3:c.770_771delinsGT ENSP00000483066.2:p.Phe257Cys
ENST00000688158.2:n.1505_1506delinsGT
ENST00000688922.2:c.*600_*601delinsGT ENSP00000508742.2:n.*600_*601delinsGT
ENST00000700021.1:c.725_726delinsGT ENSP00000514757.1:p.Phe242Cys
ENST00000700022.1:c.*109_*110delinsGT ENSP00000514758.1:n.*109_*110delinsGT
ENST00000700023.1:n.1928_1929delinsGT
ENST00000700024.1:n.2162_2163delinsGT
ENST00000700025.1:n.1539_1540delinsGT
ENST00000700026.1:n.407_408delinsGT
ENST00000700029.1:c.604_605delinsGT
ENST00000706954.1:c.770_771delinsGT ENSP00000516674.1:p.Phe257Cys
ENST00000706955.1:c.*805_*806delinsGT ENSP00000516675.1:n.*805_*806delinsGT
ENST00000686459.1:c.*356_*357delinsGT ENSP00000508909.1:n.*356_*357delinsGT
ENST00000688158.1:c.*881_*882delinsGT ENSP00000509254.1:n.*881_*882delinsGT
ENST00000688308.1:c.770_771delinsGT ENSP00000508752.1:p.Phe257Cys
ENST00000688922.1:c.691_692delinsGT
ENST00000693560.1:c.1289_1290delinsGT ENSP00000509861.1:p.Phe430Cys
ENST00000371953.8:c.770_771delinsGT MANE Select ENSP00000361021.3:p.Phe257Cys
ENST00000371953.7:c.770_771delinsGT ENSP00000361021.3:p.Phe257Cys
ENST00000472832.2:c.197_198delinsGT ENSP00000483066.1:p.Phe66Cys
NM_000314.5:c.770_771delinsGT NP_000305.3:p.Phe257Cys
NM_000314.6:c.770_771delinsGT NP_000305.3:p.Phe257Cys
NM_001304717.2:c.1289_1290delinsGT NP_001291646.2:p.Phe430Cys
NM_001304718.1:c.179_180delinsGT NP_001291647.1:p.Phe60Cys
XM_006717926.2:c.725_726delinsGT XP_006717989.1:p.Phe242Cys
XM_011539981.1:c.770_771delinsGT XP_011538283.1:p.Phe257Cys
XM_011539982.1:c.674_675delinsGT XP_011538284.1:p.Phe225Cys
XR_945791.1:n.1340_1341delinsGT
NM_000314.7:c.770_771delinsGT NP_000305.3:p.Phe257Cys
NM_001304717.5:c.1289_1290delinsGT NP_001291646.4:p.Phe430Cys
NM_001304718.2:c.179_180delinsGT NP_001291647.1:p.Phe60Cys
NM_000314.8:c.770_771delinsGT MANE Select NP_000305.3:p.Phe257Cys