Canonical Allele Identifier: CA645554039
Gene: PTEN HGNC NCBI

Linked Data

COSMIC: COSM4924

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957958_87957962del , CM000672.2:g.87957958_87957962del GRCh38
NC_000010.10:g.89717715_89717719del , CM000672.1:g.89717715_89717719del GRCh37
NC_000010.9:g.89707695_89707699del NCBI36
NG_007466.2:g.99520_99524del , LRG_311:g.99520_99524del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.740_744del ENSP00000514759.2:p.Leu247CysfsTer4
ENST00000710265.1:c.740_744del ENSP00000518161.1:p.Leu247CysfsTer4
ENST00000472832.3:c.740_744del ENSP00000483066.2:p.Leu247CysfsTer4
ENST00000688158.2:n.1475_1479del
ENST00000688922.2:c.*570_*574del ENSP00000508742.2:n.*570_*574del
ENST00000700021.1:c.695_699del ENSP00000514757.1:p.Leu232CysfsTer4
ENST00000700022.1:c.*79_*83del ENSP00000514758.1:n.*79_*83del
ENST00000700023.1:n.1898_1902del
ENST00000700024.1:n.2132_2136del
ENST00000700025.1:n.1509_1513del
ENST00000700026.1:n.377_381del
ENST00000700029.1:c.574_578del
ENST00000706954.1:c.740_744del ENSP00000516674.1:p.Leu247CysfsTer4
ENST00000706955.1:c.*775_*779del ENSP00000516675.1:n.*775_*779del
ENST00000686459.1:c.*326_*330del ENSP00000508909.1:n.*326_*330del
ENST00000688158.1:c.*851_*855del ENSP00000509254.1:n.*851_*855del
ENST00000688308.1:c.740_744del ENSP00000508752.1:p.Leu247CysfsTer4
ENST00000688922.1:c.661_665del
ENST00000693560.1:c.1259_1263del ENSP00000509861.1:p.Leu420CysfsTer4
ENST00000371953.8:c.740_744del MANE Select ENSP00000361021.3:p.Leu247CysfsTer4
ENST00000371953.7:c.740_744del ENSP00000361021.3:p.Leu247CysfsTer4
ENST00000472832.2:c.167_171del ENSP00000483066.1:p.Leu56CysfsTer4
NM_000314.5:c.740_744del NP_000305.3:p.Leu247CysfsTer4
NM_000314.6:c.740_744del NP_000305.3:p.Leu247CysfsTer4
NM_001304717.2:c.1259_1263del NP_001291646.2:p.Leu420CysfsTer4
NM_001304718.1:c.149_153del NP_001291647.1:p.Leu50CysfsTer4
XM_006717926.2:c.695_699del XP_006717989.1:p.Leu232CysfsTer4
XM_011539981.1:c.740_744del XP_011538283.1:p.Leu247CysfsTer4
XM_011539982.1:c.644_648del XP_011538284.1:p.Leu215CysfsTer4
XR_945791.1:n.1310_1314del
NM_000314.7:c.740_744del NP_000305.3:p.Leu247CysfsTer4
NM_001304717.5:c.1259_1263del NP_001291646.4:p.Leu420CysfsTer4
NM_001304718.2:c.149_153del NP_001291647.1:p.Leu50CysfsTer4
NM_000314.8:c.740_744del MANE Select NP_000305.3:p.Leu247CysfsTer4