Canonical Allele Identifier: CA2400237507
Gene: CHEK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.28694079T= , CM000684.2:g.28694079T= GRCh38
NC_000022.10:g.29090067T= , CM000684.1:g.29090067T= GRCh37
NC_000022.9:g.27420067T= NCBI36
NG_008150.1:g.52756A=
NG_008150.2:g.52788A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000711048.1:c.*149A= ENSP00000518557.1:n.*149A=
ENST00000402731.6:c.1213A= ENSP00000384835.2:p.Lys405=
ENST00000404276.6:c.1414A= MANE Select ENSP00000385747.1:p.Lys472=
ENST00000425190.7:c.751A= ENSP00000390244.2:p.Lys251=
ENST00000464581.6:c.754A= ENSP00000483777.2:p.Lys252=
ENST00000648295.1:n.966A=
ENST00000649563.1:c.751A= ENSP00000496928.1:p.Lys251=
ENST00000650281.1:c.1414A= ENSP00000497000.1:p.Lys472=
ENST00000328354.10:c.1414A= ENSP00000329178.6:p.Lys472=
ENST00000348295.7:c.1327A= ENSP00000329012.5:p.Lys443=
ENST00000382580.6:c.1543A= ENSP00000372023.2:p.Lys515=
ENST00000402731.5:c.1327A= ENSP00000384835.1:p.Lys443=
ENST00000403642.5:c.1141A= ENSP00000384919.1:p.Lys381=
ENST00000404276.5:c.1414A= ENSP00000385747.1:p.Lys472=
ENST00000405598.5:c.1414A= ENSP00000386087.1:p.Lys472=
ENST00000416671.5:c.*904A= ENSP00000402225.1:n.*904A=
ENST00000417588.5:c.1323A= ENSP00000412901.1:n.1323A=
ENST00000433728.5:c.1352A= ENSP00000404400.1:n.1352A=
ENST00000434810.5:c.612A=
ENST00000448511.5:c.1304A= ENSP00000404567.1:n.1304A=
ENST00000456369.5:c.264-4864A=
NM_001005735.1:c.1543A= NP_001005735.1:p.Lys515=
NM_001257387.1:c.751A= NP_001244316.1:p.Lys251=
NM_007194.3:c.1414A= NP_009125.1:p.Lys472=
NM_145862.2:c.1327A= NP_665861.1:p.Lys443=
XM_006724114.2:c.934A= XP_006724177.1:p.Lys312=
XM_006724116.2:c.871A= XP_006724179.2:p.Lys291=
XM_011529839.1:c.1573A= XP_011528141.1:p.Lys525=
XM_011529840.1:c.1486A= XP_011528142.1:p.Lys496=
XM_011529841.1:c.1342A= XP_011528143.1:p.Lys448=
XM_011529842.1:c.1243A= XP_011528144.1:p.Lys415=
XM_011529843.1:c.1213A= XP_011528145.1:p.Lys405=
XM_011529845.1:c.751A= XP_011528147.1:p.Lys251=
XR_937805.1:n.1573A=
NM_001349956.1:c.1213A= NP_001336885.1:p.Lys405=
NM_007194.4:c.1414A= MANE Select NP_009125.1:p.Lys472=
XM_006724114.3:c.967A= XP_006724177.2:p.Lys323=
XM_011529839.2:c.1573A= XP_011528141.1:p.Lys525=
XM_011529840.3:c.1486A= XP_011528142.1:p.Lys496=
XM_011529842.2:c.1243A= XP_011528144.1:p.Lys415=
XM_011529845.2:c.751A= XP_011528147.1:p.Lys251=
XM_017028560.1:c.1537A= XP_016884049.1:p.Lys513=
XM_017028561.2:c.751A= XP_016884050.1:p.Lys251=
XM_024452148.1:c.1444A= XP_024307916.1:p.Lys482=
XM_024452149.1:c.1357A= XP_024307917.1:p.Lys453=
XR_937805.2:n.1584A=
NM_001005735.2:c.1543A= NP_001005735.1:p.Lys515=
NM_001257387.2:c.751A= NP_001244316.1:p.Lys251=
NM_001349956.2:c.1213A= NP_001336885.1:p.Lys405=