Canonical Allele Identifier: CA2400257200

Gene: CHEK2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.28735223A= , CM000684.2:g.28735223A=	GRCh38
NC_000022.10:g.29131211A= , CM000684.1:g.29131211A=	GRCh37
NC_000022.9:g.27461211A=	NCBI36
NG_008150.1:g.11612T=
NG_008150.2:g.11644T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711048.1:c.-6-496T=	ENSP00000518557.1:n.-6-496T=
ENST00000398017.3:c.-6-496T=	ENSP00000381099.3:n.-6-496T=
ENST00000404276.6:c.-6-496T= MANE Select	ENSP00000385747.1:n.-6-496T=
ENST00000425190.7:c.-345+6546T=	ENSP00000390244.2:n.-345+6546T=
ENST00000649563.1:c.-72+6546T=	ENSP00000496928.1:n.-72+6546T=
ENST00000650233.1:c.-6-496T=	ENSP00000497699.1:n.-6-496T=
ENST00000650281.1:c.-6-496T=	ENSP00000497000.1:n.-6-496T=
ENST00000328354.10:c.-6-496T=	ENSP00000329178.6:n.-6-496T=
ENST00000348295.7:c.-6-496T=	ENSP00000329012.5:n.-6-496T=
ENST00000382565.5:c.-6-496T=	ENSP00000372006.2:n.-6-496T=
ENST00000382580.6:c.-6-496T=	ENSP00000372023.2:n.-6-496T=
ENST00000398017.2:c.25-496T=	ENSP00000381099.2:n.25-496T=
ENST00000405598.5:c.-6-496T=	ENSP00000386087.1:n.-6-496T=
ENST00000416671.5:c.-6-496T=	ENSP00000402225.1:n.-6-496T=
ENST00000425190.6:c.-345+6546T=	ENSP00000390244.1:n.-345+6546T=
ENST00000433028.6:c.-6-496T=	ENSP00000403659.1:n.-6-496T=
ENST00000439200.5:c.-6-496T=	ENSP00000408065.1:n.-6-496T=
NM_001005735.1:c.-6-496T=	NP_001005735.1:n.-6-496T=
NM_001257387.1:c.-783-496T=	NP_001244316.1:n.-783-496T=
NM_007194.3:c.-6-496T=	NP_009125.1:n.-6-496T=
NM_145862.2:c.-6-496T=	NP_665861.1:n.-6-496T=
XM_011529839.1:c.25-496T=	XP_011528141.1:n.25-496T=
XM_011529840.1:c.25-496T=	XP_011528142.1:n.25-496T=
XM_011529841.1:c.-6-496T=	XP_011528143.1:n.-6-496T=
XM_011529842.1:c.25-496T=	XP_011528144.1:n.25-496T=
XM_011529843.1:c.-6-496T=	XP_011528145.1:n.-6-496T=
XM_011529844.1:c.25-496T=	XP_011528146.1:n.25-496T=
XM_011529845.1:c.-345+6546T=	XP_011528147.1:n.-345+6546T=
XR_937805.1:n.87-496T=
XR_937806.1:n.82-496T=
XR_937807.1:n.82-496T=
NM_001349956.1:c.-6-496T=	NP_001336885.1:n.-6-496T=
NM_007194.4:c.-6-496T= MANE Select	NP_009125.1:n.-6-496T=
XM_011529839.2:c.25-496T=	XP_011528141.1:n.25-496T=
XM_011529840.3:c.25-496T=	XP_011528142.1:n.25-496T=
XM_011529842.2:c.25-496T=	XP_011528144.1:n.25-496T=
XM_011529844.2:c.25-496T=	XP_011528146.1:n.25-496T=
XM_011529845.2:c.-345+6546T=	XP_011528147.1:n.-345+6546T=
XM_017028560.1:c.25-496T=	XP_016884049.1:n.25-496T=
XM_024452148.1:c.25-496T=	XP_024307916.1:n.25-496T=
XM_024452149.1:c.25-496T=	XP_024307917.1:n.25-496T=
XR_937805.2:n.98-496T=
XR_937806.2:n.98-496T=
XR_937807.2:n.98-496T=
NM_001005735.2:c.-6-496T=	NP_001005735.1:n.-6-496T=
NM_001257387.2:c.-783-496T=	NP_001244316.1:n.-783-496T=
NM_001349956.2:c.-6-496T=	NP_001336885.1:n.-6-496T=