Canonical Allele Identifier: CA10588724

Gene: CHEK2

Linked Data

• ClinVar Variation Id: 265327
• ClinVar RCV Id: RCV000255649 ; RCV001358222 ; RCV002518758
• dbSNP Id: rs17879961
• MyVariant Identifiers: chr22:g.29121087A>C (hg19) ; chr22:g.28725099A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.28725099A>C , CM000684.2:g.28725099A>C	GRCh38
NC_000022.10:g.29121087A>C , CM000684.1:g.29121087A>C	GRCh37
NC_000022.9:g.27451087A>C	NCBI36
NG_008150.1:g.21736T>G
NG_008150.2:g.21768T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000439346.6:c.470T>G	ENSP00000396903.2:p.Ile157Ser
ENST00000454252.2:c.*450T>G	ENSP00000387451.2:n.*450T>G
ENST00000711048.1:c.470T>G	ENSP00000518557.1:p.Ile157Ser
ENST00000398017.3:c.470T>G	ENSP00000381099.3:p.Ile157Ser
ENST00000402731.6:c.444+144T>G	ENSP00000384835.2:n.444+144T>G
ENST00000404276.6:c.470T>G MANE Select	ENSP00000385747.1:p.Ile157Ser
ENST00000425190.7:c.-194T>G	ENSP00000390244.2:n.-194T>G
ENST00000649563.1:c.-71-5614T>G	ENSP00000496928.1:n.-71-5614T>G
ENST00000650233.1:c.470T>G	ENSP00000497699.1:p.Ile157Ser
ENST00000650281.1:c.470T>G	ENSP00000497000.1:p.Ile157Ser
ENST00000328354.10:c.470T>G	ENSP00000329178.6:p.Ile157Ser
ENST00000348295.7:c.470T>G	ENSP00000329012.5:p.Ile157Ser
ENST00000382565.5:c.470T>G	ENSP00000372006.2:p.Ile157Ser
ENST00000382580.6:c.599T>G	ENSP00000372023.2:p.Ile200Ser
ENST00000398017.2:c.500T>G	ENSP00000381099.2:p.Ile167Ser
ENST00000402731.5:c.470T>G	ENSP00000384835.1:p.Ile157Ser
ENST00000403642.5:c.320-5614T>G	ENSP00000384919.1:n.320-5614T>G
ENST00000404276.5:c.470T>G	ENSP00000385747.1:p.Ile157Ser
ENST00000405598.5:c.470T>G	ENSP00000386087.1:p.Ile157Ser
ENST00000416671.5:c.470T>G	ENSP00000402225.1:p.Ile157Ser
ENST00000417588.5:c.470T>G	ENSP00000412901.1:p.Ile157Ser
ENST00000425190.6:c.-194T>G	ENSP00000390244.1:n.-194T>G
ENST00000433028.6:c.444+144T>G	ENSP00000403659.1:n.444+144T>G
ENST00000433728.5:c.470T>G	ENSP00000404400.1:p.Ile157Ser
ENST00000439200.5:c.563T>G	ENSP00000408065.1:p.Ile188Ser
ENST00000439346.5:c.32T>G	ENSP00000396903.1:p.Ile11Ser
ENST00000447421.5:c.444+144T>G	ENSP00000397478.2:n.444+144T>G
ENST00000448511.5:c.444+144T>G	ENSP00000404567.1:n.444+144T>G
ENST00000454252.1:c.588T>G	ENSP00000387451.1:n.588T>G
NM_001005735.1:c.599T>G	NP_001005735.1:p.Ile200Ser
NM_001257387.1:c.-308T>G	NP_001244316.1:n.-308T>G
NM_007194.3:c.470T>G	NP_009125.1:p.Ile157Ser
NM_145862.2:c.470T>G	NP_665861.1:p.Ile157Ser
XM_011529839.1:c.629T>G	XP_011528141.1:p.Ile210Ser
XM_011529840.1:c.629T>G	XP_011528142.1:p.Ile210Ser
XM_011529841.1:c.573+144T>G	XP_011528143.1:n.573+144T>G
XM_011529842.1:c.474+144T>G	XP_011528144.1:n.474+144T>G
XM_011529843.1:c.444+144T>G	XP_011528145.1:n.444+144T>G
XM_011529844.1:c.629T>G	XP_011528146.1:p.Ile210Ser
XM_011529845.1:c.-194T>G	XP_011528147.1:n.-194T>G
XR_937805.1:n.691T>G
XR_937806.1:n.686T>G
XR_937807.1:n.686T>G
NM_001349956.1:c.444+144T>G	NP_001336885.1:n.444+144T>G
NM_007194.4:c.470T>G MANE Select	NP_009125.1:p.Ile157Ser
XM_011529839.2:c.629T>G	XP_011528141.1:p.Ile210Ser
XM_011529840.3:c.629T>G	XP_011528142.1:p.Ile210Ser
XM_011529842.2:c.474+144T>G	XP_011528144.1:n.474+144T>G
XM_011529844.2:c.629T>G	XP_011528146.1:p.Ile210Ser
XM_011529845.2:c.-194T>G	XP_011528147.1:n.-194T>G
XM_017028560.1:c.593T>G	XP_016884049.1:p.Ile198Ser
XM_024452148.1:c.500T>G	XP_024307916.1:p.Ile167Ser
XM_024452149.1:c.500T>G	XP_024307917.1:p.Ile167Ser
XR_937805.2:n.702T>G
XR_937806.2:n.702T>G
XR_937807.2:n.702T>G
NM_001005735.2:c.599T>G	NP_001005735.1:p.Ile200Ser
NM_001257387.2:c.-308T>G	NP_001244316.1:n.-308T>G
NM_001349956.2:c.444+144T>G	NP_001336885.1:n.444+144T>G