Canonical Allele Identifier: CA16616569

Gene: CHEK2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.28719435C>T , CM000684.2:g.28719435C>T	GRCh38
NC_000022.10:g.29115423C>T , CM000684.1:g.29115423C>T	GRCh37
NC_000022.9:g.27445423C>T	NCBI36
NG_008150.1:g.27400G>A
NG_008150.2:g.27432G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_007194.4:c.643G>A MANE Select	NP_009125.1:p.Ala215Thr
ENST00000404276.6:c.643G>A MANE Select	ENSP00000385747.1:p.Ala215Thr
NM_001005735.1:c.772G>A	NP_001005735.1:p.Ala258Thr
NM_001005735.2:c.772G>A	NP_001005735.1:p.Ala258Thr
NM_001257387.1:c.-21G>A	NP_001244316.1:n.-21G>A
NM_001257387.2:c.-21G>A	NP_001244316.1:n.-21G>A
NM_001349956.1:c.482+5451G>A	NP_001336885.1:n.482+5451G>A
NM_001349956.2:c.482+5451G>A	NP_001336885.1:n.482+5451G>A
NM_007194.3:c.643G>A	NP_009125.1:p.Ala215Thr
NM_145862.2:c.643G>A	NP_665861.1:p.Ala215Thr
ENST00000328354.10:c.643G>A	ENSP00000329178.6:p.Ala215Thr
ENST00000348295.7:c.643G>A	ENSP00000329012.5:p.Ala215Thr
ENST00000382580.6:c.772G>A	ENSP00000372023.2:p.Ala258Thr
ENST00000402731.5:c.643G>A	ENSP00000384835.1:p.Ala215Thr
ENST00000402731.6:c.482+5451G>A	ENSP00000384835.2:n.482+5451G>A
ENST00000403642.5:c.370G>A	ENSP00000384919.1:p.Ala124Thr
ENST00000404276.5:c.643G>A	ENSP00000385747.1:p.Ala215Thr
ENST00000405598.5:c.643G>A	ENSP00000386087.1:p.Ala215Thr
ENST00000416671.5:c.*133G>A	ENSP00000402225.1:n.*133G>A
ENST00000417588.5:c.592+5542G>A	ENSP00000412901.1:n.592+5542G>A
ENST00000425190.6:c.-21G>A	ENSP00000390244.1:n.-21G>A
ENST00000425190.7:c.-21G>A	ENSP00000390244.2:n.-21G>A
ENST00000433028.6:c.*368G>A	ENSP00000403659.1:n.*368G>A
ENST00000433728.5:c.643G>A	ENSP00000404400.1:p.Ala215Thr
ENST00000439200.5:c.736G>A	ENSP00000408065.1:p.Ala246Thr
ENST00000439346.5:c.154+5542G>A	ENSP00000396903.1:n.154+5542G>A
ENST00000439346.6:c.592+5542G>A	ENSP00000396903.2:n.592+5542G>A
ENST00000447421.5:c.482+5451G>A	ENSP00000397478.2:n.482+5451G>A
ENST00000448511.5:c.533G>A	ENSP00000404567.1:n.533G>A
ENST00000649563.1:c.-21G>A	ENSP00000496928.1:n.-21G>A
ENST00000650281.1:c.643G>A	ENSP00000497000.1:p.Ala215Thr
ENST00000711048.1:c.643G>A	ENSP00000518557.1:p.Ala215Thr
XM_011529839.1:c.802G>A	XP_011528141.1:p.Ala268Thr
XM_011529839.2:c.802G>A	XP_011528141.1:p.Ala268Thr
XM_011529840.1:c.802G>A	XP_011528142.1:p.Ala268Thr
XM_011529840.3:c.802G>A	XP_011528142.1:p.Ala268Thr
XM_011529841.1:c.611+5451G>A	XP_011528143.1:n.611+5451G>A
XM_011529842.1:c.512+5451G>A	XP_011528144.1:n.512+5451G>A
XM_011529842.2:c.512+5451G>A	XP_011528144.1:n.512+5451G>A
XM_011529843.1:c.482+5451G>A	XP_011528145.1:n.482+5451G>A
XM_011529844.1:c.802G>A	XP_011528146.1:p.Ala268Thr
XM_011529844.2:c.802G>A	XP_011528146.1:p.Ala268Thr
XM_011529845.1:c.-21G>A	XP_011528147.1:n.-21G>A
XM_011529845.2:c.-21G>A	XP_011528147.1:n.-21G>A
XM_017028560.1:c.766G>A	XP_016884049.1:p.Ala256Thr
XM_017028561.2:c.-21G>A	XP_016884050.1:n.-21G>A
XM_024452148.1:c.673G>A	XP_024307916.1:p.Ala225Thr
XM_024452149.1:c.673G>A	XP_024307917.1:p.Ala225Thr
XR_937805.1:n.864G>A
XR_937805.2:n.875G>A
XR_937806.1:n.859G>A
XR_937806.2:n.875G>A
XR_937807.1:n.859G>A
XR_937807.2:n.875G>A