Canonical Allele Identifier: CA1024870084

Gene: CHEK2

Linked Data

• dbSNP Id: rs951989487
• gnomAD v3: 22-28719002-G-C
• gnomAD v4: 22-28719002-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.28719002G>C , CM000684.2:g.28719002G>C	GRCh38
NC_000022.10:g.29114990G>C , CM000684.1:g.29114990G>C	GRCh37
NC_000022.9:g.27444990G>C	NCBI36
NG_008150.1:g.27833C>G
NG_008150.2:g.27865C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000439346.6:c.592+5975C>G	ENSP00000396903.2:n.592+5975C>G
ENST00000711048.1:c.683+393C>G	ENSP00000518557.1:n.683+393C>G
ENST00000402731.6:c.482+5884C>G	ENSP00000384835.2:n.482+5884C>G
ENST00000404276.6:c.683+393C>G MANE Select	ENSP00000385747.1:n.683+393C>G
ENST00000425190.7:c.20+393C>G	ENSP00000390244.2:n.20+393C>G
ENST00000649563.1:c.20+393C>G	ENSP00000496928.1:n.20+393C>G
ENST00000650281.1:c.683+393C>G	ENSP00000497000.1:n.683+393C>G
ENST00000328354.10:c.683+393C>G	ENSP00000329178.6:n.683+393C>G
ENST00000348295.7:c.683+393C>G	ENSP00000329012.5:n.683+393C>G
ENST00000382580.6:c.812+393C>G	ENSP00000372023.2:n.812+393C>G
ENST00000402731.5:c.683+393C>G	ENSP00000384835.1:n.683+393C>G
ENST00000403642.5:c.410+393C>G	ENSP00000384919.1:n.410+393C>G
ENST00000404276.5:c.683+393C>G	ENSP00000385747.1:n.683+393C>G
ENST00000405598.5:c.683+393C>G	ENSP00000386087.1:n.683+393C>G
ENST00000416671.5:c.*173+393C>G	ENSP00000402225.1:n.*173+393C>G
ENST00000417588.5:c.592+5975C>G	ENSP00000412901.1:n.592+5975C>G
ENST00000425190.6:c.20+393C>G	ENSP00000390244.1:n.20+393C>G
ENST00000433028.6:c.*408+393C>G	ENSP00000403659.1:n.*408+393C>G
ENST00000433728.5:c.683+393C>G	ENSP00000404400.1:n.683+393C>G
ENST00000439200.5:c.776+393C>G	ENSP00000408065.1:n.776+393C>G
ENST00000439346.5:c.154+5975C>G	ENSP00000396903.1:n.154+5975C>G
ENST00000447421.5:c.482+5884C>G	ENSP00000397478.2:n.482+5884C>G
ENST00000448511.5:c.573+393C>G	ENSP00000404567.1:n.573+393C>G
NM_001005735.1:c.812+393C>G	NP_001005735.1:n.812+393C>G
NM_001257387.1:c.20+393C>G	NP_001244316.1:n.20+393C>G
NM_007194.3:c.683+393C>G	NP_009125.1:n.683+393C>G
NM_145862.2:c.683+393C>G	NP_665861.1:n.683+393C>G
XM_011529839.1:c.842+393C>G	XP_011528141.1:n.842+393C>G
XM_011529840.1:c.842+393C>G	XP_011528142.1:n.842+393C>G
XM_011529841.1:c.611+5884C>G	XP_011528143.1:n.611+5884C>G
XM_011529842.1:c.512+5884C>G	XP_011528144.1:n.512+5884C>G
XM_011529843.1:c.482+5884C>G	XP_011528145.1:n.482+5884C>G
XM_011529844.1:c.842+393C>G	XP_011528146.1:n.842+393C>G
XM_011529845.1:c.20+393C>G	XP_011528147.1:n.20+393C>G
XR_937805.1:n.904+393C>G
XR_937806.1:n.899+393C>G
XR_937807.1:n.899+393C>G
NM_001349956.1:c.482+5884C>G	NP_001336885.1:n.482+5884C>G
NM_007194.4:c.683+393C>G MANE Select	NP_009125.1:n.683+393C>G
XM_011529839.2:c.842+393C>G	XP_011528141.1:n.842+393C>G
XM_011529840.3:c.842+393C>G	XP_011528142.1:n.842+393C>G
XM_011529842.2:c.512+5884C>G	XP_011528144.1:n.512+5884C>G
XM_011529844.2:c.842+393C>G	XP_011528146.1:n.842+393C>G
XM_011529845.2:c.20+393C>G	XP_011528147.1:n.20+393C>G
XM_017028560.1:c.806+393C>G	XP_016884049.1:n.806+393C>G
XM_017028561.2:c.20+393C>G	XP_016884050.1:n.20+393C>G
XM_024452148.1:c.713+393C>G	XP_024307916.1:n.713+393C>G
XM_024452149.1:c.713+393C>G	XP_024307917.1:n.713+393C>G
XR_937805.2:n.915+393C>G
XR_937806.2:n.915+393C>G
XR_937807.2:n.915+393C>G
NM_001005735.2:c.812+393C>G	NP_001005735.1:n.812+393C>G
NM_001257387.2:c.20+393C>G	NP_001244316.1:n.20+393C>G
NM_001349956.2:c.482+5884C>G	NP_001336885.1:n.482+5884C>G