Canonical Allele Identifier: CA470669772
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 2674416
COSMIC: COSM5810
MyVariant Identifiers: chr10:g.89717705del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957949del , CM000672.2:g.87957949del GRCh38
NC_000010.10:g.89717706del , CM000672.1:g.89717706del GRCh37
NC_000010.9:g.89707686del NCBI36
NG_007466.2:g.99511del , LRG_311:g.99511del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.731del ENSP00000514759.2:p.Pro244LeufsTer12
ENST00000710265.1:c.731del ENSP00000518161.1:p.Pro244LeufsTer12
ENST00000472832.3:c.731del ENSP00000483066.2:p.Pro244LeufsTer12
ENST00000688158.2:n.1466del
ENST00000688922.2:c.*561del ENSP00000508742.2:n.*561del
ENST00000700021.1:c.686del ENSP00000514757.1:p.Pro229LeufsTer12
ENST00000700022.1:c.*70del ENSP00000514758.1:n.*70del
ENST00000700023.1:n.1889del
ENST00000700024.1:n.2123del
ENST00000700025.1:n.1500del
ENST00000700026.1:n.368del
ENST00000700029.1:c.565del
ENST00000706954.1:c.731del ENSP00000516674.1:p.Pro244LeufsTer12
ENST00000706955.1:c.*766del ENSP00000516675.1:n.*766del
ENST00000686459.1:c.*317del ENSP00000508909.1:n.*317del
ENST00000688158.1:c.*842del ENSP00000509254.1:n.*842del
ENST00000688308.1:c.731del ENSP00000508752.1:p.Pro244LeufsTer12
ENST00000688922.1:c.652del
ENST00000693560.1:c.1250del ENSP00000509861.1:p.Pro417LeufsTer12
ENST00000371953.8:c.731del MANE Select ENSP00000361021.3:p.Pro244LeufsTer12
ENST00000371953.7:c.731del ENSP00000361021.3:p.Pro244LeufsTer12
ENST00000472832.2:c.158del ENSP00000483066.1:p.Pro53LeufsTer12
NM_000314.5:c.731del NP_000305.3:p.Pro244LeufsTer12
NM_000314.6:c.731del NP_000305.3:p.Pro244LeufsTer12
NM_001304717.2:c.1250del NP_001291646.2:p.Pro417LeufsTer12
NM_001304718.1:c.140del NP_001291647.1:p.Pro47LeufsTer12
XM_006717926.2:c.686del XP_006717989.1:p.Pro229LeufsTer12
XM_011539981.1:c.731del XP_011538283.1:p.Pro244LeufsTer12
XM_011539982.1:c.635del XP_011538284.1:p.Pro212LeufsTer12
XR_945791.1:n.1301del
NM_000314.7:c.731del NP_000305.3:p.Pro244LeufsTer12
NM_001304717.5:c.1250del NP_001291646.4:p.Pro417LeufsTer12
NM_001304718.2:c.140del NP_001291647.1:p.Pro47LeufsTer12
NM_000314.8:c.731del MANE Select NP_000305.3:p.Pro244LeufsTer12