Canonical Allele Identifier: CA658656802

Gene: CHEK2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.28687895G>A , CM000684.2:g.28687895G>A	GRCh38
NC_000022.10:g.29083883G>A , CM000684.1:g.29083883G>A	GRCh37
NC_000022.9:g.27413883G>A	NCBI36
NG_008150.1:g.58940C>T
NG_008150.2:g.58972C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_007194.4:c.*2C>T MANE Select	NP_009125.1:n.*2C>T
ENST00000404276.6:c.*2C>T MANE Select	ENSP00000385747.1:n.*2C>T
NM_001005735.1:c.*2C>T	NP_001005735.1:n.*2C>T
NM_001005735.2:c.*2C>T	NP_001005735.1:n.*2C>T
NM_001257387.1:c.*2C>T	NP_001244316.1:n.*2C>T
NM_001257387.2:c.*2C>T	NP_001244316.1:n.*2C>T
NM_001349956.1:c.*2C>T	NP_001336885.1:n.*2C>T
NM_001349956.2:c.*2C>T	NP_001336885.1:n.*2C>T
NM_007194.3:c.*2C>T	NP_009125.1:n.*2C>T
NM_145862.2:c.*2C>T	NP_665861.1:n.*2C>T
ENST00000328354.10:c.*2C>T	ENSP00000329178.6:n.*2C>T
ENST00000348295.7:c.*2C>T	ENSP00000329012.5:n.*2C>T
ENST00000382580.6:c.*2C>T	ENSP00000372023.2:n.*2C>T
ENST00000402731.6:c.*2C>T	ENSP00000384835.2:n.*2C>T
ENST00000404276.5:c.1634C>T	ENSP00000385747.1:n.1634C>T
ENST00000405598.5:c.*2C>T	ENSP00000386087.1:n.*2C>T
ENST00000416671.5:c.*1124C>T	ENSP00000402225.1:n.*1124C>T
ENST00000417588.5:c.1543C>T	ENSP00000412901.1:n.1543C>T
ENST00000425190.7:c.*2C>T	ENSP00000390244.2:n.*2C>T
ENST00000433728.5:c.1572C>T	ENSP00000404400.1:n.1572C>T
ENST00000434810.5:c.832C>T
ENST00000448511.5:c.1524C>T	ENSP00000404567.1:n.1524C>T
ENST00000456369.5:c.436C>T
ENST00000464581.6:c.*2C>T	ENSP00000483777.2:n.*2C>T
ENST00000472807.1:n.368C>T
ENST00000648295.1:n.1186C>T
ENST00000649563.1:c.*2C>T	ENSP00000496928.1:n.*2C>T
ENST00000650281.1:c.*2C>T	ENSP00000497000.1:n.*2C>T
ENST00000711048.1:c.*369C>T	ENSP00000518557.1:n.*369C>T
XM_006724114.2:c.*2C>T	XP_006724177.1:n.*2C>T
XM_006724114.3:c.*2C>T	XP_006724177.2:n.*2C>T
XM_006724116.2:c.*2C>T	XP_006724179.2:n.*2C>T
XM_011529839.1:c.1793C>T	XP_011528141.1:n.1793C>T
XM_011529839.2:c.*2C>T	XP_011528141.1:n.*2C>T
XM_011529840.1:c.*2C>T	XP_011528142.1:n.*2C>T
XM_011529840.3:c.*2C>T	XP_011528142.1:n.*2C>T
XM_011529841.1:c.*2C>T	XP_011528143.1:n.*2C>T
XM_011529842.1:c.1463C>T	XP_011528144.1:n.1463C>T
XM_011529842.2:c.*2C>T	XP_011528144.1:n.*2C>T
XM_011529843.1:c.*2C>T	XP_011528145.1:n.*2C>T
XM_011529845.1:c.*2C>T	XP_011528147.1:n.*2C>T
XM_011529845.2:c.*2C>T	XP_011528147.1:n.*2C>T
XM_017028560.1:c.*2C>T	XP_016884049.1:n.*2C>T
XM_017028561.2:c.*2C>T	XP_016884050.1:n.*2C>T
XM_024452148.1:c.*2C>T	XP_024307916.1:n.*2C>T
XM_024452149.1:c.*2C>T	XP_024307917.1:n.*2C>T
XR_937805.1:n.1793C>T
XR_937805.2:n.1804C>T