Canonical Allele Identifier: CA2400238828
Gene: CHEK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.28696926G= , CM000684.2:g.28696926G= GRCh38
NC_000022.10:g.29092914G= , CM000684.1:g.29092914G= GRCh37
NC_000022.9:g.27422914G= NCBI36
NG_008150.1:g.49909C=
NG_008150.2:g.49941C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000711048.1:c.1009-1684C= ENSP00000518557.1:n.1009-1684C=
ENST00000402731.6:c.869C= ENSP00000384835.2:p.Ser290=
ENST00000404276.6:c.1070C= MANE Select ENSP00000385747.1:p.Ser357=
ENST00000425190.7:c.407C= ENSP00000390244.2:p.Ser136=
ENST00000464581.6:c.410C= ENSP00000483777.2:p.Ser137=
ENST00000648295.1:n.622C=
ENST00000649563.1:c.407C= ENSP00000496928.1:p.Ser136=
ENST00000650281.1:c.1070C= ENSP00000497000.1:p.Ser357=
ENST00000328354.10:c.1070C= ENSP00000329178.6:p.Ser357=
ENST00000348295.7:c.1009-1053C= ENSP00000329012.5:n.1009-1053C=
ENST00000382580.6:c.1199C= ENSP00000372023.2:p.Ser400=
ENST00000402731.5:c.1009-1053C= ENSP00000384835.1:n.1009-1053C=
ENST00000403642.5:c.797C= ENSP00000384919.1:p.Ser266=
ENST00000404276.5:c.1070C= ENSP00000385747.1:p.Ser357=
ENST00000405598.5:c.1070C= ENSP00000386087.1:p.Ser357=
ENST00000416671.5:c.*560C= ENSP00000402225.1:n.*560C=
ENST00000417588.5:c.979C= ENSP00000412901.1:n.979C=
ENST00000433028.6:c.*795C= ENSP00000403659.1:n.*795C=
ENST00000433728.5:c.1008C= ENSP00000404400.1:n.1008C=
ENST00000434810.5:c.301C=
ENST00000447421.5:c.869C= ENSP00000397478.2:p.Ser290=
ENST00000448511.5:c.960C= ENSP00000404567.1:n.960C=
ENST00000456369.5:c.263+2912C=
ENST00000464581.5:c.410C= ENSP00000483777.1:p.Ser137=
NM_001005735.1:c.1199C= NP_001005735.1:p.Ser400=
NM_001257387.1:c.407C= NP_001244316.1:p.Ser136=
NM_007194.3:c.1070C= NP_009125.1:p.Ser357=
NM_145862.2:c.1009-1053C= NP_665861.1:n.1009-1053C=
XM_006724114.2:c.590C= XP_006724177.1:p.Ser197=
XM_006724116.2:c.527C= XP_006724179.2:p.Ser176=
XM_011529839.1:c.1229C= XP_011528141.1:p.Ser410=
XM_011529840.1:c.1168-1053C= XP_011528142.1:n.1168-1053C=
XM_011529841.1:c.998C= XP_011528143.1:p.Ser333=
XM_011529842.1:c.899C= XP_011528144.1:p.Ser300=
XM_011529843.1:c.869C= XP_011528145.1:p.Ser290=
XM_011529845.1:c.407C= XP_011528147.1:p.Ser136=
XR_937805.1:n.1229C=
XR_937806.1:n.1163-1053C=
NM_001349956.1:c.869C= NP_001336885.1:p.Ser290=
NM_007194.4:c.1070C= MANE Select NP_009125.1:p.Ser357=
XM_006724114.3:c.623C= XP_006724177.2:p.Ser208=
XM_011529839.2:c.1229C= XP_011528141.1:p.Ser410=
XM_011529840.3:c.1168-1053C= XP_011528142.1:n.1168-1053C=
XM_011529842.2:c.899C= XP_011528144.1:p.Ser300=
XM_011529845.2:c.407C= XP_011528147.1:p.Ser136=
XM_017028560.1:c.1193C= XP_016884049.1:p.Ser398=
XM_017028561.2:c.407C= XP_016884050.1:p.Ser136=
XM_024452148.1:c.1100C= XP_024307916.1:p.Ser367=
XM_024452149.1:c.1039-1053C= XP_024307917.1:n.1039-1053C=
XR_937805.2:n.1240C=
XR_937806.2:n.1179-1053C=
NM_001005735.2:c.1199C= NP_001005735.1:p.Ser400=
NM_001257387.2:c.407C= NP_001244316.1:p.Ser136=
NM_001349956.2:c.869C= NP_001336885.1:p.Ser290=