Canonical Allele Identifier: CA2695200885
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 2674370
ClinVar RCV Id: RCV003452566

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957961del , CM000672.2:g.87957961del GRCh38
NC_000010.10:g.89717718del , CM000672.1:g.89717718del GRCh37
NC_000010.9:g.89707698del NCBI36
NG_007466.2:g.99523del , LRG_311:g.99523del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.743del ENSP00000514759.2:p.Pro248LeufsTer8
ENST00000710265.1:c.743del ENSP00000518161.1:p.Pro248LeufsTer8
ENST00000472832.3:c.743del ENSP00000483066.2:p.Pro248LeufsTer8
ENST00000688158.2:n.1478del
ENST00000688922.2:c.*573del ENSP00000508742.2:n.*573del
ENST00000700021.1:c.698del ENSP00000514757.1:p.Pro233LeufsTer8
ENST00000700022.1:c.*82del ENSP00000514758.1:n.*82del
ENST00000700023.1:n.1901del
ENST00000700024.1:n.2135del
ENST00000700025.1:n.1512del
ENST00000700026.1:n.380del
ENST00000700029.1:c.577del
ENST00000706954.1:c.743del ENSP00000516674.1:p.Pro248LeufsTer8
ENST00000706955.1:c.*778del ENSP00000516675.1:n.*778del
ENST00000686459.1:c.*329del ENSP00000508909.1:n.*329del
ENST00000688158.1:c.*854del ENSP00000509254.1:n.*854del
ENST00000688308.1:c.743del ENSP00000508752.1:p.Pro248LeufsTer8
ENST00000688922.1:c.664del
ENST00000693560.1:c.1262del ENSP00000509861.1:p.Pro421LeufsTer8
ENST00000371953.8:c.743del MANE Select ENSP00000361021.3:p.Pro248LeufsTer8
ENST00000371953.7:c.743del ENSP00000361021.3:p.Pro248LeufsTer8
ENST00000472832.2:c.170del ENSP00000483066.1:p.Pro57LeufsTer8
NM_000314.5:c.743del NP_000305.3:p.Pro248LeufsTer8
NM_000314.6:c.743del NP_000305.3:p.Pro248LeufsTer8
NM_001304717.2:c.1262del NP_001291646.2:p.Pro421LeufsTer8
NM_001304718.1:c.152del NP_001291647.1:p.Pro51LeufsTer8
XM_006717926.2:c.698del XP_006717989.1:p.Pro233LeufsTer8
XM_011539981.1:c.743del XP_011538283.1:p.Pro248LeufsTer8
XM_011539982.1:c.647del XP_011538284.1:p.Pro216LeufsTer8
XR_945791.1:n.1313del
NM_000314.7:c.743del NP_000305.3:p.Pro248LeufsTer8
NM_001304717.5:c.1262del NP_001291646.4:p.Pro421LeufsTer8
NM_001304718.2:c.152del NP_001291647.1:p.Pro51LeufsTer8
NM_000314.8:c.743del MANE Select NP_000305.3:p.Pro248LeufsTer8