Canonical Allele Identifier: CA891839989
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957988_87957989delinsAA , CM000672.2:g.87957988_87957989delinsAA GRCh38
NC_000010.10:g.89717745_89717746delinsAA , CM000672.1:g.89717745_89717746delinsAA GRCh37
NC_000010.9:g.89707725_89707726delinsAA NCBI36
NG_007466.2:g.99550_99551delinsAA , LRG_311:g.99550_99551delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.770_771delinsAA ENSP00000514759.2:p.Phe257Ter
ENST00000710265.1:c.770_771delinsAA ENSP00000518161.1:p.Phe257Ter
ENST00000472832.3:c.770_771delinsAA ENSP00000483066.2:p.Phe257Ter
ENST00000688158.2:n.1505_1506delinsAA
ENST00000688922.2:c.*600_*601delinsAA ENSP00000508742.2:n.*600_*601delinsAA
ENST00000700021.1:c.725_726delinsAA ENSP00000514757.1:p.Phe242Ter
ENST00000700022.1:c.*109_*110delinsAA ENSP00000514758.1:n.*109_*110delinsAA
ENST00000700023.1:n.1928_1929delinsAA
ENST00000700024.1:n.2162_2163delinsAA
ENST00000700025.1:n.1539_1540delinsAA
ENST00000700026.1:n.407_408delinsAA
ENST00000700029.1:c.604_605delinsAA
ENST00000706954.1:c.770_771delinsAA ENSP00000516674.1:p.Phe257Ter
ENST00000706955.1:c.*805_*806delinsAA ENSP00000516675.1:n.*805_*806delinsAA
ENST00000686459.1:c.*356_*357delinsAA ENSP00000508909.1:n.*356_*357delinsAA
ENST00000688158.1:c.*881_*882delinsAA ENSP00000509254.1:n.*881_*882delinsAA
ENST00000688308.1:c.770_771delinsAA ENSP00000508752.1:p.Phe257Ter
ENST00000688922.1:c.691_692delinsAA
ENST00000693560.1:c.1289_1290delinsAA ENSP00000509861.1:p.Phe430Ter
ENST00000371953.8:c.770_771delinsAA MANE Select ENSP00000361021.3:p.Phe257Ter
ENST00000371953.7:c.770_771delinsAA ENSP00000361021.3:p.Phe257Ter
ENST00000472832.2:c.197_198delinsAA ENSP00000483066.1:p.Phe66Ter
NM_000314.5:c.770_771delinsAA NP_000305.3:p.Phe257Ter
NM_000314.6:c.770_771delinsAA NP_000305.3:p.Phe257Ter
NM_001304717.2:c.1289_1290delinsAA NP_001291646.2:p.Phe430Ter
NM_001304718.1:c.179_180delinsAA NP_001291647.1:p.Phe60Ter
XM_006717926.2:c.725_726delinsAA XP_006717989.1:p.Phe242Ter
XM_011539981.1:c.770_771delinsAA XP_011538283.1:p.Phe257Ter
XM_011539982.1:c.674_675delinsAA XP_011538284.1:p.Phe225Ter
XR_945791.1:n.1340_1341delinsAA
NM_000314.7:c.770_771delinsAA NP_000305.3:p.Phe257Ter
NM_001304717.5:c.1289_1290delinsAA NP_001291646.4:p.Phe430Ter
NM_001304718.2:c.179_180delinsAA NP_001291647.1:p.Phe60Ter
NM_000314.8:c.770_771delinsAA MANE Select NP_000305.3:p.Phe257Ter