Canonical Allele Identifier: CA645554136
Gene: PTEN HGNC NCBI

Linked Data

COSMIC: COSM5775
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961094_87961095delinsTT , CM000672.2:g.87961094_87961095delinsTT GRCh38
NC_000010.10:g.89720851_89720852delinsTT , CM000672.1:g.89720851_89720852delinsTT GRCh37
NC_000010.9:g.89710831_89710832delinsTT NCBI36
NG_007466.2:g.102656_102657delinsTT , LRG_311:g.102656_102657delinsTT

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.1095_1096delinsTT ENSP00000514759.2:p.Asn366Ter
ENST00000710265.1:c.1002_1003delinsTT ENSP00000518161.1:p.Asn335Ter
ENST00000472832.3:c.1002_1003delinsTT ENSP00000483066.2:p.Asn335Ter
ENST00000688158.2:n.1737_1738delinsTT
ENST00000688922.2:c.*832_*833delinsTT ENSP00000508742.2:n.*832_*833delinsTT
ENST00000700021.1:c.957_958delinsTT ENSP00000514757.1:p.Asn320Ter
ENST00000700022.1:c.*341_*342delinsTT ENSP00000514758.1:n.*341_*342delinsTT
ENST00000700023.1:n.2160_2161delinsTT
ENST00000700024.1:n.2394_2395delinsTT
ENST00000700025.1:n.1771_1772delinsTT
ENST00000700026.1:n.639_640delinsTT
ENST00000706954.1:c.1002_1003delinsTT ENSP00000516674.1:p.Asn335Ter
ENST00000706955.1:c.*1037_*1038delinsTT ENSP00000516675.1:n.*1037_*1038delinsTT
ENST00000686459.1:c.*588_*589delinsTT ENSP00000508909.1:n.*588_*589delinsTT
ENST00000688158.1:c.*1113_*1114delinsTT ENSP00000509254.1:n.*1113_*1114delinsTT
ENST00000688308.1:c.1002_1003delinsTT ENSP00000508752.1:p.Asn335Ter
ENST00000688922.1:c.923_924delinsTT
ENST00000693560.1:c.1521_1522delinsTT ENSP00000509861.1:p.Asn508Ter
ENST00000371953.8:c.1002_1003delinsTT MANE Select ENSP00000361021.3:p.Asn335Ter
ENST00000371953.7:c.1002_1003delinsTT ENSP00000361021.3:p.Asn335Ter
ENST00000472832.2:c.429_430delinsTT ENSP00000483066.1:p.Asn144Ter
NM_000314.5:c.1002_1003delinsTT NP_000305.3:p.Asn335Ter
NM_000314.6:c.1002_1003delinsTT NP_000305.3:p.Asn335Ter
NM_001304717.2:c.1521_1522delinsTT NP_001291646.2:p.Asn508Ter
NM_001304718.1:c.411_412delinsTT NP_001291647.1:p.Asn138Ter
XM_006717926.2:c.957_958delinsTT XP_006717989.1:p.Asn320Ter
XM_011539981.1:c.1002_1003delinsTT XP_011538283.1:p.Asn335Ter
XM_011539982.1:c.906_907delinsTT XP_011538284.1:p.Asn303Ter
XR_945791.1:n.1572_1573delinsTT
NM_000314.7:c.1002_1003delinsTT NP_000305.3:p.Asn335Ter
NM_001304717.5:c.1521_1522delinsTT NP_001291646.4:p.Asn508Ter
NM_001304718.2:c.411_412delinsTT NP_001291647.1:p.Asn138Ter
NM_000314.8:c.1002_1003delinsTT MANE Select NP_000305.3:p.Asn335Ter
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