Canonical Allele Identifier: CA000397
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 189447
ClinVar RCV Id: RCV000169840
dbSNP Id: rs786204899

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87933080del , CM000672.2:g.87933080del GRCh38
NC_000010.10:g.89692837del , CM000672.1:g.89692837del GRCh37
NC_000010.9:g.89682817del NCBI36
NG_007466.2:g.74642del , LRG_311:g.74642del

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.321del ENSP00000514759.2:p.Asp109ThrfsTer4
ENST00000710265.1:c.321del ENSP00000518161.1:p.Asp109ThrfsTer4
ENST00000472832.3:c.321del ENSP00000483066.2:p.Asp109ThrfsTer4
ENST00000688158.2:n.1056del
ENST00000688922.2:c.*151del ENSP00000508742.2:n.*151del
ENST00000700021.1:c.276del ENSP00000514757.1:p.Asp94ThrfsTer4
ENST00000700022.1:c.321del ENSP00000514758.1:p.Asp109ThrfsTer4
ENST00000700029.1:c.155del
ENST00000706954.1:c.321del ENSP00000516674.1:p.Asp109ThrfsTer4
ENST00000706955.1:c.*356del ENSP00000516675.1:n.*356del
ENST00000686459.1:c.321del ENSP00000508909.1:p.Asp109ThrfsTer4
ENST00000688158.1:c.*432del ENSP00000509254.1:n.*432del
ENST00000688308.1:c.321del ENSP00000508752.1:p.Asp109ThrfsTer4
ENST00000688922.1:c.242del
ENST00000693560.1:c.840del ENSP00000509861.1:p.Asp282ThrfsTer4
ENST00000371953.8:c.321del MANE Select ENSP00000361021.3:p.Asp109ThrfsTer4
ENST00000371953.7:c.321del ENSP00000361021.3:p.Asp109ThrfsTer4
ENST00000498703.1:n.147del
ENST00000610634.1:c.219del ENSP00000477517.1:p.Asp75ThrfsTer4
NM_000314.5:c.321del NP_000305.3:p.Asp109ThrfsTer4
NM_000314.6:c.321del NP_000305.3:p.Asp109ThrfsTer4
NM_001304717.2:c.840del NP_001291646.2:p.Asp282ThrfsTer4
NM_001304718.1:c.-430del NP_001291647.1:n.-430del
XM_006717926.2:c.276del XP_006717989.1:p.Asp94ThrfsTer4
XM_011539981.1:c.321del XP_011538283.1:p.Asp109ThrfsTer4
XM_011539982.1:c.225del XP_011538284.1:p.Asp77ThrfsTer4
XR_945789.1:n.1033del
XR_945790.1:n.1033del
XR_945791.1:n.1033del
NM_000314.7:c.321del NP_000305.3:p.Asp109ThrfsTer4
NM_001304717.5:c.840del NP_001291646.4:p.Asp282ThrfsTer4
NM_001304718.2:c.-430del NP_001291647.1:n.-430del
NM_000314.8:c.321del MANE Select NP_000305.3:p.Asp109ThrfsTer4