Canonical Allele Identifier: CA2400240178

Gene: CHEK2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.28699851A= , CM000684.2:g.28699851A=	GRCh38
NC_000022.10:g.29095839A= , CM000684.1:g.29095839A=	GRCh37
NC_000022.9:g.27425839A=	NCBI36
NG_008150.1:g.46984T=
NG_008150.2:g.47016T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439346.6:c.904T=	ENSP00000396903.2:n.904T=
ENST00000711048.1:c.995T=	ENSP00000518557.1:p.Leu332=
ENST00000402731.6:c.794T=	ENSP00000384835.2:p.Leu265=
ENST00000404276.6:c.995T= MANE Select	ENSP00000385747.1:p.Leu332=
ENST00000425190.7:c.332T=	ENSP00000390244.2:p.Leu111=
ENST00000464581.6:c.335T=	ENSP00000483777.2:p.Leu112=
ENST00000648295.1:n.547T=
ENST00000649563.1:c.332T=	ENSP00000496928.1:p.Leu111=
ENST00000650281.1:c.995T=	ENSP00000497000.1:p.Leu332=
ENST00000328354.10:c.995T=	ENSP00000329178.6:p.Leu332=
ENST00000348295.7:c.995T=	ENSP00000329012.5:p.Leu332=
ENST00000382580.6:c.1124T=	ENSP00000372023.2:p.Leu375=
ENST00000402731.5:c.995T=	ENSP00000384835.1:p.Leu332=
ENST00000403642.5:c.722T=	ENSP00000384919.1:p.Leu241=
ENST00000404276.5:c.995T=	ENSP00000385747.1:p.Leu332=
ENST00000405598.5:c.995T=	ENSP00000386087.1:p.Leu332=
ENST00000416671.5:c.*485T=	ENSP00000402225.1:n.*485T=
ENST00000417588.5:c.904T=	ENSP00000412901.1:n.904T=
ENST00000425190.6:c.332T=	ENSP00000390244.1:p.Leu111=
ENST00000433028.6:c.*720T=	ENSP00000403659.1:n.*720T=
ENST00000433728.5:c.933T=	ENSP00000404400.1:n.933T=
ENST00000434810.5:c.226T=
ENST00000439346.5:c.466T=	ENSP00000396903.1:n.466T=
ENST00000447421.5:c.794T=	ENSP00000397478.2:p.Leu265=
ENST00000448511.5:c.885T=	ENSP00000404567.1:n.885T=
ENST00000456369.5:c.250T=
ENST00000464581.5:c.335T=	ENSP00000483777.1:p.Leu112=
ENST00000491919.5:n.552T=
NM_001005735.1:c.1124T=	NP_001005735.1:p.Leu375=
NM_001257387.1:c.332T=	NP_001244316.1:p.Leu111=
NM_007194.3:c.995T=	NP_009125.1:p.Leu332=
NM_145862.2:c.995T=	NP_665861.1:p.Leu332=
XM_006724114.2:c.515T=	XP_006724177.1:p.Leu172=
XM_006724116.2:c.452T=	XP_006724179.2:p.Leu151=
XM_011529839.1:c.1154T=	XP_011528141.1:p.Leu385=
XM_011529840.1:c.1154T=	XP_011528142.1:p.Leu385=
XM_011529841.1:c.923T=	XP_011528143.1:p.Leu308=
XM_011529842.1:c.824T=	XP_011528144.1:p.Leu275=
XM_011529843.1:c.794T=	XP_011528145.1:p.Leu265=
XM_011529844.1:c.1154T=	XP_011528146.1:p.Leu385=
XM_011529845.1:c.332T=	XP_011528147.1:p.Leu111=
XR_937805.1:n.1154T=
XR_937806.1:n.1149T=
XR_937807.1:n.1149T=
NM_001349956.1:c.794T=	NP_001336885.1:p.Leu265=
NM_007194.4:c.995T= MANE Select	NP_009125.1:p.Leu332=
XM_006724114.3:c.548T=	XP_006724177.2:p.Leu183=
XM_011529839.2:c.1154T=	XP_011528141.1:p.Leu385=
XM_011529840.3:c.1154T=	XP_011528142.1:p.Leu385=
XM_011529842.2:c.824T=	XP_011528144.1:p.Leu275=
XM_011529844.2:c.1154T=	XP_011528146.1:p.Leu385=
XM_011529845.2:c.332T=	XP_011528147.1:p.Leu111=
XM_017028560.1:c.1118T=	XP_016884049.1:p.Leu373=
XM_017028561.2:c.332T=	XP_016884050.1:p.Leu111=
XM_024452148.1:c.1025T=	XP_024307916.1:p.Leu342=
XM_024452149.1:c.1025T=	XP_024307917.1:p.Leu342=
XR_937805.2:n.1165T=
XR_937806.2:n.1165T=
XR_937807.2:n.1165T=
NM_001005735.2:c.1124T=	NP_001005735.1:p.Leu375=
NM_001257387.2:c.332T=	NP_001244316.1:p.Leu111=
NM_001349956.2:c.794T=	NP_001336885.1:p.Leu265=