Canonical Allele Identifier: CA411099912

Gene: CHEK2

Linked Data

• MyVariant Identifiers: chr22:g.29095887T>G (hg19) ; chr22:g.28699899T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.28699899T>G , CM000684.2:g.28699899T>G	GRCh38
NC_000022.10:g.29095887T>G , CM000684.1:g.29095887T>G	GRCh37
NC_000022.9:g.27425887T>G	NCBI36
NG_008150.1:g.46936A>C
NG_008150.2:g.46968A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439346.6:c.856A>C	ENSP00000396903.2:n.856A>C
ENST00000711048.1:c.947A>C	ENSP00000518557.1:p.Asn316Thr
ENST00000402731.6:c.746A>C	ENSP00000384835.2:p.Asn249Thr
ENST00000404276.6:c.947A>C MANE Select	ENSP00000385747.1:p.Asn316Thr
ENST00000425190.7:c.284A>C	ENSP00000390244.2:p.Asn95Thr
ENST00000464581.6:c.287A>C	ENSP00000483777.2:p.Asn96Thr
ENST00000648295.1:n.499A>C
ENST00000649563.1:c.284A>C	ENSP00000496928.1:p.Asn95Thr
ENST00000650281.1:c.947A>C	ENSP00000497000.1:p.Asn316Thr
ENST00000328354.10:c.947A>C	ENSP00000329178.6:p.Asn316Thr
ENST00000348295.7:c.947A>C	ENSP00000329012.5:p.Asn316Thr
ENST00000382580.6:c.1076A>C	ENSP00000372023.2:p.Asn359Thr
ENST00000402731.5:c.947A>C	ENSP00000384835.1:p.Asn316Thr
ENST00000403642.5:c.674A>C	ENSP00000384919.1:p.Asn225Thr
ENST00000404276.5:c.947A>C	ENSP00000385747.1:p.Asn316Thr
ENST00000405598.5:c.947A>C	ENSP00000386087.1:p.Asn316Thr
ENST00000416671.5:c.*437A>C	ENSP00000402225.1:n.*437A>C
ENST00000417588.5:c.856A>C	ENSP00000412901.1:n.856A>C
ENST00000425190.6:c.284A>C	ENSP00000390244.1:p.Asn95Thr
ENST00000433028.6:c.*672A>C	ENSP00000403659.1:n.*672A>C
ENST00000433728.5:c.885A>C	ENSP00000404400.1:n.885A>C
ENST00000434810.5:c.178A>C
ENST00000439346.5:c.418A>C	ENSP00000396903.1:n.418A>C
ENST00000447421.5:c.746A>C	ENSP00000397478.2:p.Asn249Thr
ENST00000448511.5:c.837A>C	ENSP00000404567.1:n.837A>C
ENST00000456369.5:c.202A>C
ENST00000464581.5:c.287A>C	ENSP00000483777.1:p.Asn96Thr
ENST00000491919.5:n.504A>C
NM_001005735.1:c.1076A>C	NP_001005735.1:p.Asn359Thr
NM_001257387.1:c.284A>C	NP_001244316.1:p.Asn95Thr
NM_007194.3:c.947A>C	NP_009125.1:p.Asn316Thr
NM_145862.2:c.947A>C	NP_665861.1:p.Asn316Thr
XM_006724114.2:c.467A>C	XP_006724177.1:p.Asn156Thr
XM_006724116.2:c.404A>C	XP_006724179.2:p.Asn135Thr
XM_011529839.1:c.1106A>C	XP_011528141.1:p.Asn369Thr
XM_011529840.1:c.1106A>C	XP_011528142.1:p.Asn369Thr
XM_011529841.1:c.875A>C	XP_011528143.1:p.Asn292Thr
XM_011529842.1:c.776A>C	XP_011528144.1:p.Asn259Thr
XM_011529843.1:c.746A>C	XP_011528145.1:p.Asn249Thr
XM_011529844.1:c.1106A>C	XP_011528146.1:p.Asn369Thr
XM_011529845.1:c.284A>C	XP_011528147.1:p.Asn95Thr
XR_937805.1:n.1106A>C
XR_937806.1:n.1101A>C
XR_937807.1:n.1101A>C
NM_001349956.1:c.746A>C	NP_001336885.1:p.Asn249Thr
NM_007194.4:c.947A>C MANE Select	NP_009125.1:p.Asn316Thr
XM_006724114.3:c.500A>C	XP_006724177.2:p.Asn167Thr
XM_011529839.2:c.1106A>C	XP_011528141.1:p.Asn369Thr
XM_011529840.3:c.1106A>C	XP_011528142.1:p.Asn369Thr
XM_011529842.2:c.776A>C	XP_011528144.1:p.Asn259Thr
XM_011529844.2:c.1106A>C	XP_011528146.1:p.Asn369Thr
XM_011529845.2:c.284A>C	XP_011528147.1:p.Asn95Thr
XM_017028560.1:c.1070A>C	XP_016884049.1:p.Asn357Thr
XM_017028561.2:c.284A>C	XP_016884050.1:p.Asn95Thr
XM_024452148.1:c.977A>C	XP_024307916.1:p.Asn326Thr
XM_024452149.1:c.977A>C	XP_024307917.1:p.Asn326Thr
XR_937805.2:n.1117A>C
XR_937806.2:n.1117A>C
XR_937807.2:n.1117A>C
NM_001005735.2:c.1076A>C	NP_001005735.1:p.Asn359Thr
NM_001257387.2:c.284A>C	NP_001244316.1:p.Asn95Thr
NM_001349956.2:c.746A>C	NP_001336885.1:p.Asn249Thr