Canonical Allele Identifier: CA2400240198
Gene: CHEK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.28699872T= , CM000684.2:g.28699872T= GRCh38
NC_000022.10:g.29095860T= , CM000684.1:g.29095860T= GRCh37
NC_000022.9:g.27425860T= NCBI36
NG_008150.1:g.46963A=
NG_008150.2:g.46995A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000439346.6:c.883A= ENSP00000396903.2:n.883A=
ENST00000711048.1:c.974A= ENSP00000518557.1:p.Lys325=
ENST00000402731.6:c.773A= ENSP00000384835.2:p.Lys258=
ENST00000404276.6:c.974A= MANE Select ENSP00000385747.1:p.Lys325=
ENST00000425190.7:c.311A= ENSP00000390244.2:p.Lys104=
ENST00000464581.6:c.314A= ENSP00000483777.2:p.Lys105=
ENST00000648295.1:n.526A=
ENST00000649563.1:c.311A= ENSP00000496928.1:p.Lys104=
ENST00000650281.1:c.974A= ENSP00000497000.1:p.Lys325=
ENST00000328354.10:c.974A= ENSP00000329178.6:p.Lys325=
ENST00000348295.7:c.974A= ENSP00000329012.5:p.Lys325=
ENST00000382580.6:c.1103A= ENSP00000372023.2:p.Lys368=
ENST00000402731.5:c.974A= ENSP00000384835.1:p.Lys325=
ENST00000403642.5:c.701A= ENSP00000384919.1:p.Lys234=
ENST00000404276.5:c.974A= ENSP00000385747.1:p.Lys325=
ENST00000405598.5:c.974A= ENSP00000386087.1:p.Lys325=
ENST00000416671.5:c.*464A= ENSP00000402225.1:n.*464A=
ENST00000417588.5:c.883A= ENSP00000412901.1:n.883A=
ENST00000425190.6:c.311A= ENSP00000390244.1:p.Lys104=
ENST00000433028.6:c.*699A= ENSP00000403659.1:n.*699A=
ENST00000433728.5:c.912A= ENSP00000404400.1:n.912A=
ENST00000434810.5:c.205A=
ENST00000439346.5:c.445A= ENSP00000396903.1:n.445A=
ENST00000447421.5:c.773A= ENSP00000397478.2:p.Lys258=
ENST00000448511.5:c.864A= ENSP00000404567.1:n.864A=
ENST00000456369.5:c.229A=
ENST00000464581.5:c.314A= ENSP00000483777.1:p.Lys105=
ENST00000491919.5:n.531A=
NM_001005735.1:c.1103A= NP_001005735.1:p.Lys368=
NM_001257387.1:c.311A= NP_001244316.1:p.Lys104=
NM_007194.3:c.974A= NP_009125.1:p.Lys325=
NM_145862.2:c.974A= NP_665861.1:p.Lys325=
XM_006724114.2:c.494A= XP_006724177.1:p.Lys165=
XM_006724116.2:c.431A= XP_006724179.2:p.Lys144=
XM_011529839.1:c.1133A= XP_011528141.1:p.Lys378=
XM_011529840.1:c.1133A= XP_011528142.1:p.Lys378=
XM_011529841.1:c.902A= XP_011528143.1:p.Lys301=
XM_011529842.1:c.803A= XP_011528144.1:p.Lys268=
XM_011529843.1:c.773A= XP_011528145.1:p.Lys258=
XM_011529844.1:c.1133A= XP_011528146.1:p.Lys378=
XM_011529845.1:c.311A= XP_011528147.1:p.Lys104=
XR_937805.1:n.1133A=
XR_937806.1:n.1128A=
XR_937807.1:n.1128A=
NM_001349956.1:c.773A= NP_001336885.1:p.Lys258=
NM_007194.4:c.974A= MANE Select NP_009125.1:p.Lys325=
XM_006724114.3:c.527A= XP_006724177.2:p.Lys176=
XM_011529839.2:c.1133A= XP_011528141.1:p.Lys378=
XM_011529840.3:c.1133A= XP_011528142.1:p.Lys378=
XM_011529842.2:c.803A= XP_011528144.1:p.Lys268=
XM_011529844.2:c.1133A= XP_011528146.1:p.Lys378=
XM_011529845.2:c.311A= XP_011528147.1:p.Lys104=
XM_017028560.1:c.1097A= XP_016884049.1:p.Lys366=
XM_017028561.2:c.311A= XP_016884050.1:p.Lys104=
XM_024452148.1:c.1004A= XP_024307916.1:p.Lys335=
XM_024452149.1:c.1004A= XP_024307917.1:p.Lys335=
XR_937805.2:n.1144A=
XR_937806.2:n.1144A=
XR_937807.2:n.1144A=
NM_001005735.2:c.1103A= NP_001005735.1:p.Lys368=
NM_001257387.2:c.311A= NP_001244316.1:p.Lys104=
NM_001349956.2:c.773A= NP_001336885.1:p.Lys258=