Canonical Allele Identifier: CA2400240186

Gene: CHEK2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.28699857T= , CM000684.2:g.28699857T=	GRCh38
NC_000022.10:g.29095845T= , CM000684.1:g.29095845T=	GRCh37
NC_000022.9:g.27425845T=	NCBI36
NG_008150.1:g.46978A=
NG_008150.2:g.47010A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439346.6:c.898A=	ENSP00000396903.2:n.898A=
ENST00000711048.1:c.989A=	ENSP00000518557.1:p.Gln330=
ENST00000402731.6:c.788A=	ENSP00000384835.2:p.Gln263=
ENST00000404276.6:c.989A= MANE Select	ENSP00000385747.1:p.Gln330=
ENST00000425190.7:c.326A=	ENSP00000390244.2:p.Gln109=
ENST00000464581.6:c.329A=	ENSP00000483777.2:p.Gln110=
ENST00000648295.1:n.541A=
ENST00000649563.1:c.326A=	ENSP00000496928.1:p.Gln109=
ENST00000650281.1:c.989A=	ENSP00000497000.1:p.Gln330=
ENST00000328354.10:c.989A=	ENSP00000329178.6:p.Gln330=
ENST00000348295.7:c.989A=	ENSP00000329012.5:p.Gln330=
ENST00000382580.6:c.1118A=	ENSP00000372023.2:p.Gln373=
ENST00000402731.5:c.989A=	ENSP00000384835.1:p.Gln330=
ENST00000403642.5:c.716A=	ENSP00000384919.1:p.Gln239=
ENST00000404276.5:c.989A=	ENSP00000385747.1:p.Gln330=
ENST00000405598.5:c.989A=	ENSP00000386087.1:p.Gln330=
ENST00000416671.5:c.*479A=	ENSP00000402225.1:n.*479A=
ENST00000417588.5:c.898A=	ENSP00000412901.1:n.898A=
ENST00000425190.6:c.326A=	ENSP00000390244.1:p.Gln109=
ENST00000433028.6:c.*714A=	ENSP00000403659.1:n.*714A=
ENST00000433728.5:c.927A=	ENSP00000404400.1:n.927A=
ENST00000434810.5:c.220A=
ENST00000439346.5:c.460A=	ENSP00000396903.1:n.460A=
ENST00000447421.5:c.788A=	ENSP00000397478.2:p.Gln263=
ENST00000448511.5:c.879A=	ENSP00000404567.1:n.879A=
ENST00000456369.5:c.244A=
ENST00000464581.5:c.329A=	ENSP00000483777.1:p.Gln110=
ENST00000491919.5:n.546A=
NM_001005735.1:c.1118A=	NP_001005735.1:p.Gln373=
NM_001257387.1:c.326A=	NP_001244316.1:p.Gln109=
NM_007194.3:c.989A=	NP_009125.1:p.Gln330=
NM_145862.2:c.989A=	NP_665861.1:p.Gln330=
XM_006724114.2:c.509A=	XP_006724177.1:p.Gln170=
XM_006724116.2:c.446A=	XP_006724179.2:p.Gln149=
XM_011529839.1:c.1148A=	XP_011528141.1:p.Gln383=
XM_011529840.1:c.1148A=	XP_011528142.1:p.Gln383=
XM_011529841.1:c.917A=	XP_011528143.1:p.Gln306=
XM_011529842.1:c.818A=	XP_011528144.1:p.Gln273=
XM_011529843.1:c.788A=	XP_011528145.1:p.Gln263=
XM_011529844.1:c.1148A=	XP_011528146.1:p.Gln383=
XM_011529845.1:c.326A=	XP_011528147.1:p.Gln109=
XR_937805.1:n.1148A=
XR_937806.1:n.1143A=
XR_937807.1:n.1143A=
NM_001349956.1:c.788A=	NP_001336885.1:p.Gln263=
NM_007194.4:c.989A= MANE Select	NP_009125.1:p.Gln330=
XM_006724114.3:c.542A=	XP_006724177.2:p.Gln181=
XM_011529839.2:c.1148A=	XP_011528141.1:p.Gln383=
XM_011529840.3:c.1148A=	XP_011528142.1:p.Gln383=
XM_011529842.2:c.818A=	XP_011528144.1:p.Gln273=
XM_011529844.2:c.1148A=	XP_011528146.1:p.Gln383=
XM_011529845.2:c.326A=	XP_011528147.1:p.Gln109=
XM_017028560.1:c.1112A=	XP_016884049.1:p.Gln371=
XM_017028561.2:c.326A=	XP_016884050.1:p.Gln109=
XM_024452148.1:c.1019A=	XP_024307916.1:p.Gln340=
XM_024452149.1:c.1019A=	XP_024307917.1:p.Gln340=
XR_937805.2:n.1159A=
XR_937806.2:n.1159A=
XR_937807.2:n.1159A=
NM_001005735.2:c.1118A=	NP_001005735.1:p.Gln373=
NM_001257387.2:c.326A=	NP_001244316.1:p.Gln109=
NM_001349956.2:c.788A=	NP_001336885.1:p.Gln263=