Canonical Allele Identifier: CA891837745
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965386_87965387delinsGT , CM000672.2:g.87965386_87965387delinsGT GRCh38
NC_000010.10:g.89725143_89725144delinsGT , CM000672.1:g.89725143_89725144delinsGT GRCh37
NC_000010.9:g.89715123_89715124delinsGT NCBI36
NG_007466.2:g.106948_106949delinsGT , LRG_311:g.106948_106949delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1219_1220delinsGT ENSP00000514759.2:p.His407Val
ENST00000710265.1:c.*155_*156delinsGT ENSP00000518161.1:n.*155_*156delinsGT
ENST00000688158.2:n.1861_1862delinsGT
ENST00000688922.2:c.*956_*957delinsGT ENSP00000508742.2:n.*956_*957delinsGT
ENST00000700021.1:c.1081_1082delinsGT ENSP00000514757.1:p.His361Val
ENST00000700022.1:c.*465_*466delinsGT ENSP00000514758.1:n.*465_*466delinsGT
ENST00000700023.1:n.2284_2285delinsGT
ENST00000700024.1:n.2518_2519delinsGT
ENST00000706954.1:c.1126_1127delinsGT ENSP00000516674.1:p.His376Val
ENST00000706955.1:c.*1161_*1162delinsGT ENSP00000516675.1:n.*1161_*1162delinsGT
ENST00000686459.1:c.*712_*713delinsGT ENSP00000508909.1:n.*712_*713delinsGT
ENST00000688158.1:c.*1237_*1238delinsGT ENSP00000509254.1:n.*1237_*1238delinsGT
ENST00000688308.1:c.1126_1127delinsGT ENSP00000508752.1:p.His376Val
ENST00000688922.1:c.1047_1048delinsGT
ENST00000693560.1:c.1645_1646delinsGT ENSP00000509861.1:p.His549Val
ENST00000371953.8:c.1126_1127delinsGT MANE Select ENSP00000361021.3:p.His376Val
ENST00000371953.7:c.1126_1127delinsGT ENSP00000361021.3:p.His376Val
NM_000314.5:c.1126_1127delinsGT NP_000305.3:p.His376Val
NM_000314.6:c.1126_1127delinsGT NP_000305.3:p.His376Val
NM_001304717.2:c.1645_1646delinsGT NP_001291646.2:p.His549Val
NM_001304718.1:c.535_536delinsGT NP_001291647.1:p.His179Val
XM_006717926.2:c.1081_1082delinsGT XP_006717989.1:p.His361Val
XM_011539982.1:c.1030_1031delinsGT XP_011538284.1:p.His344Val
XR_945791.1:n.1696_1697delinsGT
NM_000314.7:c.1126_1127delinsGT NP_000305.3:p.His376Val
NM_001304717.5:c.1645_1646delinsGT NP_001291646.4:p.His549Val
NM_001304718.2:c.535_536delinsGT NP_001291647.1:p.His179Val
NM_000314.8:c.1126_1127delinsGT MANE Select NP_000305.3:p.His376Val