Canonical Allele Identifier: CA470974105
Gene: PTEN HGNC NCBI

Linked Data

COSMIC: COSM5814
MyVariant Identifiers: chr10:g.89720842del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961085del , CM000672.2:g.87961085del GRCh38
NC_000010.10:g.89720842del , CM000672.1:g.89720842del GRCh37
NC_000010.9:g.89710822del NCBI36
NG_007466.2:g.102647del , LRG_311:g.102647del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1086del ENSP00000514759.2:p.Asp362GlufsTer13
ENST00000710265.1:c.993del ENSP00000518161.1:p.Asp331GlufsTer16
ENST00000472832.3:c.993del ENSP00000483066.2:p.Asp331GlufsTer?
ENST00000688158.2:n.1728del
ENST00000688922.2:c.*823del ENSP00000508742.2:n.*823del
ENST00000700021.1:c.948del ENSP00000514757.1:p.Asp316GlufsTer13
ENST00000700022.1:c.*332del ENSP00000514758.1:n.*332del
ENST00000700023.1:n.2151del
ENST00000700024.1:n.2385del
ENST00000700025.1:n.1762del
ENST00000700026.1:n.630del
ENST00000706954.1:c.993del ENSP00000516674.1:p.Asp331GlufsTer13
ENST00000706955.1:c.*1028del ENSP00000516675.1:n.*1028del
ENST00000686459.1:c.*579del ENSP00000508909.1:n.*579del
ENST00000688158.1:c.*1104del ENSP00000509254.1:n.*1104del
ENST00000688308.1:c.993del ENSP00000508752.1:p.Asp331GlufsTer13
ENST00000688922.1:c.914del
ENST00000693560.1:c.1512del ENSP00000509861.1:p.Asp504GlufsTer13
ENST00000371953.8:c.993del MANE Select ENSP00000361021.3:p.Asp331GlufsTer13
ENST00000371953.7:c.993del ENSP00000361021.3:p.Asp331GlufsTer13
ENST00000472832.2:c.420del ENSP00000483066.1:p.Asp140GlufsTer?
NM_000314.5:c.993del NP_000305.3:p.Asp331GlufsTer13
NM_000314.6:c.993del NP_000305.3:p.Asp331GlufsTer13
NM_001304717.2:c.1512del NP_001291646.2:p.Asp504GlufsTer13
NM_001304718.1:c.402del NP_001291647.1:p.Asp134GlufsTer13
XM_006717926.2:c.948del XP_006717989.1:p.Asp316GlufsTer13
XM_011539981.1:c.993del XP_011538283.1:p.Asp331GlufsTer16
XM_011539982.1:c.897del XP_011538284.1:p.Asp299GlufsTer13
XR_945791.1:n.1563del
NM_000314.7:c.993del NP_000305.3:p.Asp331GlufsTer13
NM_001304717.5:c.1512del NP_001291646.4:p.Asp504GlufsTer13
NM_001304718.2:c.402del NP_001291647.1:p.Asp134GlufsTer13
NM_000314.8:c.993del MANE Select NP_000305.3:p.Asp331GlufsTer13