Canonical Allele Identifier: CA2579926397
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965458_87965459delinsTC , CM000672.2:g.87965458_87965459delinsTC GRCh38
NC_000010.10:g.89725215_89725216delinsTC , CM000672.1:g.89725215_89725216delinsTC GRCh37
NC_000010.9:g.89715195_89715196delinsTC NCBI36
NG_007466.2:g.107020_107021delinsTC , LRG_311:g.107020_107021delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1291_1292delinsTC ENSP00000514759.2:p.Ile431Ser
ENST00000710265.1:c.*227_*228delinsTC ENSP00000518161.1:n.*227_*228delinsTC
ENST00000688158.2:n.1933_1934delinsTC
ENST00000688922.2:c.*1028_*1029delinsTC ENSP00000508742.2:n.*1028_*1029delinsTC
ENST00000700021.1:c.1153_1154delinsTC ENSP00000514757.1:p.Ile385Ser
ENST00000700022.1:c.*537_*538delinsTC ENSP00000514758.1:n.*537_*538delinsTC
ENST00000700023.1:n.2356_2357delinsTC
ENST00000700024.1:n.2590_2591delinsTC
ENST00000706954.1:c.1198_1199delinsTC ENSP00000516674.1:p.Ile400Ser
ENST00000706955.1:c.*1233_*1234delinsTC ENSP00000516675.1:n.*1233_*1234delinsTC
ENST00000686459.1:c.*784_*785delinsTC ENSP00000508909.1:n.*784_*785delinsTC
ENST00000688158.1:c.*1309_*1310delinsTC ENSP00000509254.1:n.*1309_*1310delinsTC
ENST00000688308.1:c.1198_1199delinsTC ENSP00000508752.1:p.Ile400Ser
ENST00000688922.1:c.1119_1120delinsTC
ENST00000693560.1:c.1717_1718delinsTC ENSP00000509861.1:p.Ile573Ser
ENST00000371953.8:c.1198_1199delinsTC MANE Select ENSP00000361021.3:p.Ile400Ser
ENST00000371953.7:c.1198_1199delinsTC ENSP00000361021.3:p.Ile400Ser
NM_000314.5:c.1198_1199delinsTC NP_000305.3:p.Ile400Ser
NM_000314.6:c.1198_1199delinsTC NP_000305.3:p.Ile400Ser
NM_001304717.2:c.1717_1718delinsTC NP_001291646.2:p.Ile573Ser
NM_001304718.1:c.607_608delinsTC NP_001291647.1:p.Ile203Ser
XM_006717926.2:c.1153_1154delinsTC XP_006717989.1:p.Ile385Ser
XM_011539982.1:c.1102_1103delinsTC XP_011538284.1:p.Ile368Ser
XR_945791.1:n.1768_1769delinsTC
NM_000314.7:c.1198_1199delinsTC NP_000305.3:p.Ile400Ser
NM_001304717.5:c.1717_1718delinsTC NP_001291646.4:p.Ile573Ser
NM_001304718.2:c.607_608delinsTC NP_001291647.1:p.Ile203Ser
NM_000314.8:c.1198_1199delinsTC MANE Select NP_000305.3:p.Ile400Ser