Canonical Allele Identifier: CA299108
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182449
dbSNP Id: rs730881699

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.28725284del , CM000684.2:g.28725284del GRCh38
NC_000022.10:g.29121272del , CM000684.1:g.29121272del GRCh37
NC_000022.9:g.27451272del NCBI36
NG_008150.1:g.21553del
NG_008150.2:g.21585del

Transcript Alleles

HGVS Amino-acid change
ENST00000439346.6:c.405del ENSP00000396903.2:p.Lys135AsnfsTer26
ENST00000454252.2:c.*385del ENSP00000387451.2:n.*385del
ENST00000711048.1:c.405del ENSP00000518557.1:p.Lys135AsnfsTer26
ENST00000398017.3:c.405del ENSP00000381099.3:p.Lys135AsnfsTer26
ENST00000402731.6:c.405del ENSP00000384835.2:p.Lys135AsnfsTer?
ENST00000404276.6:c.405del MANE Select ENSP00000385747.1:p.Lys135AsnfsTer26
ENST00000425190.7:c.-259del ENSP00000390244.2:n.-259del
ENST00000649563.1:c.-71-5797del ENSP00000496928.1:n.-71-5797del
ENST00000650233.1:c.405del ENSP00000497699.1:p.Lys135AsnfsTer26
ENST00000650281.1:c.405del ENSP00000497000.1:p.Lys135AsnfsTer26
ENST00000328354.10:c.405del ENSP00000329178.6:p.Lys135AsnfsTer26
ENST00000348295.7:c.405del ENSP00000329012.5:p.Lys135AsnfsTer26
ENST00000382565.5:c.405del ENSP00000372006.2:p.Lys135AsnfsTer26
ENST00000382580.6:c.534del ENSP00000372023.2:p.Lys178AsnfsTer26
ENST00000398017.2:c.435del ENSP00000381099.2:p.Lys145AsnfsTer26
ENST00000402731.5:c.405del ENSP00000384835.1:p.Lys135AsnfsTer26
ENST00000403642.5:c.320-5797del ENSP00000384919.1:n.320-5797del
ENST00000404276.5:c.405del ENSP00000385747.1:p.Lys135AsnfsTer26
ENST00000405598.5:c.405del ENSP00000386087.1:p.Lys135AsnfsTer26
ENST00000416671.5:c.405del ENSP00000402225.1:p.Lys135AsnfsTer26
ENST00000417588.5:c.405del ENSP00000412901.1:p.Lys135AsnfsTer26
ENST00000425190.6:c.-259del ENSP00000390244.1:n.-259del
ENST00000433028.6:c.405del ENSP00000403659.1:p.Lys135AsnfsTer29
ENST00000433728.5:c.405del ENSP00000404400.1:p.Lys135AsnfsTer26
ENST00000439200.5:c.498del ENSP00000408065.1:p.Lys166AsnfsTer26
ENST00000447421.5:c.405del ENSP00000397478.2:p.Lys135AsnfsTer?
ENST00000448511.5:c.405del ENSP00000404567.1:p.Lys135AsnfsTer?
ENST00000454252.1:c.523del ENSP00000387451.1:n.523del
NM_001005735.1:c.534del NP_001005735.1:p.Lys178AsnfsTer26
NM_001257387.1:c.-373del NP_001244316.1:n.-373del
NM_007194.3:c.405del NP_009125.1:p.Lys135AsnfsTer26
NM_145862.2:c.405del NP_665861.1:p.Lys135AsnfsTer26
XM_011529839.1:c.564del XP_011528141.1:p.Lys188AsnfsTer26
XM_011529840.1:c.564del XP_011528142.1:p.Lys188AsnfsTer26
XM_011529841.1:c.534del XP_011528143.1:p.Lys178AsnfsTer?
XM_011529842.1:c.435del XP_011528144.1:p.Lys145AsnfsTer?
XM_011529843.1:c.405del XP_011528145.1:p.Lys135AsnfsTer?
XM_011529844.1:c.564del XP_011528146.1:p.Lys188AsnfsTer26
XM_011529845.1:c.-259del XP_011528147.1:n.-259del
XR_937805.1:n.626del
XR_937806.1:n.621del
XR_937807.1:n.621del
NM_001349956.1:c.405del NP_001336885.1:p.Lys135AsnfsTer?
NM_007194.4:c.405del MANE Select NP_009125.1:p.Lys135AsnfsTer26
XM_011529839.2:c.564del XP_011528141.1:p.Lys188AsnfsTer26
XM_011529840.3:c.564del XP_011528142.1:p.Lys188AsnfsTer26
XM_011529842.2:c.435del XP_011528144.1:p.Lys145AsnfsTer?
XM_011529844.2:c.564del XP_011528146.1:p.Lys188AsnfsTer26
XM_011529845.2:c.-259del XP_011528147.1:n.-259del
XM_017028560.1:c.528del XP_016884049.1:p.Lys176AsnfsTer26
XM_024452148.1:c.435del XP_024307916.1:p.Lys145AsnfsTer26
XM_024452149.1:c.435del XP_024307917.1:p.Lys145AsnfsTer26
XR_937805.2:n.637del
XR_937806.2:n.637del
XR_937807.2:n.637del
NM_001005735.2:c.534del NP_001005735.1:p.Lys178AsnfsTer26
NM_001257387.2:c.-373del NP_001244316.1:n.-373del
NM_001349956.2:c.405del NP_001336885.1:p.Lys135AsnfsTer?