Canonical Allele Identifier: CA658822954
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 545840
ClinVar RCV Id: RCV000657411
dbSNP Id: rs1554825224

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957962del , CM000672.2:g.87957962del GRCh38
NC_000010.10:g.89717719del , CM000672.1:g.89717719del GRCh37
NC_000010.9:g.89707699del NCBI36
NG_007466.2:g.99524del , LRG_311:g.99524del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.744del ENSP00000514759.2:p.Val249CysfsTer7
ENST00000710265.1:c.744del ENSP00000518161.1:p.Val249CysfsTer7
ENST00000472832.3:c.744del ENSP00000483066.2:p.Val249CysfsTer7
ENST00000688158.2:n.1479del
ENST00000688922.2:c.*574del ENSP00000508742.2:n.*574del
ENST00000700021.1:c.699del ENSP00000514757.1:p.Val234CysfsTer7
ENST00000700022.1:c.*83del ENSP00000514758.1:n.*83del
ENST00000700023.1:n.1902del
ENST00000700024.1:n.2136del
ENST00000700025.1:n.1513del
ENST00000700026.1:n.381del
ENST00000700029.1:c.578del
ENST00000706954.1:c.744del ENSP00000516674.1:p.Val249CysfsTer7
ENST00000706955.1:c.*779del ENSP00000516675.1:n.*779del
ENST00000686459.1:c.*330del ENSP00000508909.1:n.*330del
ENST00000688158.1:c.*855del ENSP00000509254.1:n.*855del
ENST00000688308.1:c.744del ENSP00000508752.1:p.Val249CysfsTer7
ENST00000688922.1:c.665del
ENST00000693560.1:c.1263del ENSP00000509861.1:p.Val422CysfsTer7
ENST00000371953.8:c.744del MANE Select ENSP00000361021.3:p.Val249CysfsTer7
ENST00000371953.7:c.744del ENSP00000361021.3:p.Val249CysfsTer7
ENST00000472832.2:c.171del ENSP00000483066.1:p.Val58CysfsTer7
NM_000314.5:c.744del NP_000305.3:p.Val249CysfsTer7
NM_000314.6:c.744del NP_000305.3:p.Val249CysfsTer7
NM_001304717.2:c.1263del NP_001291646.2:p.Val422CysfsTer7
NM_001304718.1:c.153del NP_001291647.1:p.Val52CysfsTer7
XM_006717926.2:c.699del XP_006717989.1:p.Val234CysfsTer7
XM_011539981.1:c.744del XP_011538283.1:p.Val249CysfsTer7
XM_011539982.1:c.648del XP_011538284.1:p.Val217CysfsTer7
XR_945791.1:n.1314del
NM_000314.7:c.744del NP_000305.3:p.Val249CysfsTer7
NM_001304717.5:c.1263del NP_001291646.4:p.Val422CysfsTer7
NM_001304718.2:c.153del NP_001291647.1:p.Val52CysfsTer7
NM_000314.8:c.744del MANE Select NP_000305.3:p.Val249CysfsTer7