Canonical Allele Identifier: CA411099480

Gene: CHEK2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.28699858G>A , CM000684.2:g.28699858G>A	GRCh38
NC_000022.10:g.29095846G>A , CM000684.1:g.29095846G>A	GRCh37
NC_000022.9:g.27425846G>A	NCBI36
NG_008150.1:g.46977C>T
NG_008150.2:g.47009C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_007194.4:c.988C>T MANE Select	NP_009125.1:p.Gln330Ter
ENST00000404276.6:c.988C>T MANE Select	ENSP00000385747.1:p.Gln330Ter
NM_001005735.1:c.1117C>T	NP_001005735.1:p.Gln373Ter
NM_001005735.2:c.1117C>T	NP_001005735.1:p.Gln373Ter
NM_001257387.1:c.325C>T	NP_001244316.1:p.Gln109Ter
NM_001257387.2:c.325C>T	NP_001244316.1:p.Gln109Ter
NM_001349956.1:c.787C>T	NP_001336885.1:p.Gln263Ter
NM_001349956.2:c.787C>T	NP_001336885.1:p.Gln263Ter
NM_007194.3:c.988C>T	NP_009125.1:p.Gln330Ter
NM_145862.2:c.988C>T	NP_665861.1:p.Gln330Ter
ENST00000328354.10:c.988C>T	ENSP00000329178.6:p.Gln330Ter
ENST00000348295.7:c.988C>T	ENSP00000329012.5:p.Gln330Ter
ENST00000382580.6:c.1117C>T	ENSP00000372023.2:p.Gln373Ter
ENST00000402731.5:c.988C>T	ENSP00000384835.1:p.Gln330Ter
ENST00000402731.6:c.787C>T	ENSP00000384835.2:p.Gln263Ter
ENST00000403642.5:c.715C>T	ENSP00000384919.1:p.Gln239Ter
ENST00000404276.5:c.988C>T	ENSP00000385747.1:p.Gln330Ter
ENST00000405598.5:c.988C>T	ENSP00000386087.1:p.Gln330Ter
ENST00000416671.5:c.*478C>T	ENSP00000402225.1:n.*478C>T
ENST00000417588.5:c.897C>T	ENSP00000412901.1:n.897C>T
ENST00000425190.6:c.325C>T	ENSP00000390244.1:p.Gln109Ter
ENST00000425190.7:c.325C>T	ENSP00000390244.2:p.Gln109Ter
ENST00000433028.6:c.*713C>T	ENSP00000403659.1:n.*713C>T
ENST00000433728.5:c.926C>T	ENSP00000404400.1:n.926C>T
ENST00000434810.5:c.219C>T
ENST00000439346.5:c.459C>T	ENSP00000396903.1:n.459C>T
ENST00000439346.6:c.897C>T	ENSP00000396903.2:n.897C>T
ENST00000447421.5:c.787C>T	ENSP00000397478.2:p.Gln263Ter
ENST00000448511.5:c.878C>T	ENSP00000404567.1:n.878C>T
ENST00000456369.5:c.243C>T
ENST00000464581.5:c.328C>T	ENSP00000483777.1:p.Gln110Ter
ENST00000464581.6:c.328C>T	ENSP00000483777.2:p.Gln110Ter
ENST00000491919.5:n.545C>T
ENST00000648295.1:n.540C>T
ENST00000649563.1:c.325C>T	ENSP00000496928.1:p.Gln109Ter
ENST00000650281.1:c.988C>T	ENSP00000497000.1:p.Gln330Ter
ENST00000711048.1:c.988C>T	ENSP00000518557.1:p.Gln330Ter
XM_006724114.2:c.508C>T	XP_006724177.1:p.Gln170Ter
XM_006724114.3:c.541C>T	XP_006724177.2:p.Gln181Ter
XM_006724116.2:c.445C>T	XP_006724179.2:p.Gln149Ter
XM_011529839.1:c.1147C>T	XP_011528141.1:p.Gln383Ter
XM_011529839.2:c.1147C>T	XP_011528141.1:p.Gln383Ter
XM_011529840.1:c.1147C>T	XP_011528142.1:p.Gln383Ter
XM_011529840.3:c.1147C>T	XP_011528142.1:p.Gln383Ter
XM_011529841.1:c.916C>T	XP_011528143.1:p.Gln306Ter
XM_011529842.1:c.817C>T	XP_011528144.1:p.Gln273Ter
XM_011529842.2:c.817C>T	XP_011528144.1:p.Gln273Ter
XM_011529843.1:c.787C>T	XP_011528145.1:p.Gln263Ter
XM_011529844.1:c.1147C>T	XP_011528146.1:p.Gln383Ter
XM_011529844.2:c.1147C>T	XP_011528146.1:p.Gln383Ter
XM_011529845.1:c.325C>T	XP_011528147.1:p.Gln109Ter
XM_011529845.2:c.325C>T	XP_011528147.1:p.Gln109Ter
XM_017028560.1:c.1111C>T	XP_016884049.1:p.Gln371Ter
XM_017028561.2:c.325C>T	XP_016884050.1:p.Gln109Ter
XM_024452148.1:c.1018C>T	XP_024307916.1:p.Gln340Ter
XM_024452149.1:c.1018C>T	XP_024307917.1:p.Gln340Ter
XR_937805.1:n.1147C>T
XR_937805.2:n.1158C>T
XR_937806.1:n.1142C>T
XR_937806.2:n.1158C>T
XR_937807.1:n.1142C>T
XR_937807.2:n.1158C>T