Canonical Allele Identifier: CA411096663

Gene: CHEK2

Linked Data

• ClinVar Variation Id: 2012927
• ClinVar RCV Id: RCV002843475
• dbSNP Id: rs2145802224
• MyVariant Identifiers: chr22:g.29091730G>C (hg19) ; chr22:g.28695742G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.28695742G>C , CM000684.2:g.28695742G>C	GRCh38
NC_000022.10:g.29091730G>C , CM000684.1:g.29091730G>C	GRCh37
NC_000022.9:g.27421730G>C	NCBI36
NG_008150.1:g.51093C>G
NG_008150.2:g.51125C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000711048.1:c.1009-500C>G	ENSP00000518557.1:n.1009-500C>G
ENST00000402731.6:c.1026C>G	ENSP00000384835.2:p.Asp342Glu
ENST00000404276.6:c.1227C>G MANE Select	ENSP00000385747.1:p.Asp409Glu
ENST00000425190.7:c.564C>G	ENSP00000390244.2:p.Asp188Glu
ENST00000464581.6:c.567C>G	ENSP00000483777.2:p.Asp189Glu
ENST00000648295.1:n.779C>G
ENST00000649563.1:c.564C>G	ENSP00000496928.1:p.Asp188Glu
ENST00000650281.1:c.1227C>G	ENSP00000497000.1:p.Asp409Glu
ENST00000328354.10:c.1227C>G	ENSP00000329178.6:p.Asp409Glu
ENST00000348295.7:c.1140C>G	ENSP00000329012.5:p.Asp380Glu
ENST00000382580.6:c.1356C>G	ENSP00000372023.2:p.Asp452Glu
ENST00000402731.5:c.1140C>G	ENSP00000384835.1:p.Asp380Glu
ENST00000403642.5:c.954C>G	ENSP00000384919.1:p.Asp318Glu
ENST00000404276.5:c.1227C>G	ENSP00000385747.1:p.Asp409Glu
ENST00000405598.5:c.1227C>G	ENSP00000386087.1:p.Asp409Glu
ENST00000416671.5:c.*717C>G	ENSP00000402225.1:n.*717C>G
ENST00000417588.5:c.1136C>G	ENSP00000412901.1:n.1136C>G
ENST00000433728.5:c.1165C>G	ENSP00000404400.1:n.1165C>G
ENST00000434810.5:c.458C>G
ENST00000448511.5:c.1117C>G	ENSP00000404567.1:n.1117C>G
ENST00000456369.5:c.263+4096C>G
NM_001005735.1:c.1356C>G	NP_001005735.1:p.Asp452Glu
NM_001257387.1:c.564C>G	NP_001244316.1:p.Asp188Glu
NM_007194.3:c.1227C>G	NP_009125.1:p.Asp409Glu
NM_145862.2:c.1140C>G	NP_665861.1:p.Asp380Glu
XM_006724114.2:c.747C>G	XP_006724177.1:p.Asp249Glu
XM_006724116.2:c.684C>G	XP_006724179.2:p.Asp228Glu
XM_011529839.1:c.1386C>G	XP_011528141.1:p.Asp462Glu
XM_011529840.1:c.1299C>G	XP_011528142.1:p.Asp433Glu
XM_011529841.1:c.1155C>G	XP_011528143.1:p.Asp385Glu
XM_011529842.1:c.1056C>G	XP_011528144.1:p.Asp352Glu
XM_011529843.1:c.1026C>G	XP_011528145.1:p.Asp342Glu
XM_011529845.1:c.564C>G	XP_011528147.1:p.Asp188Glu
XR_937805.1:n.1386C>G
NM_001349956.1:c.1026C>G	NP_001336885.1:p.Asp342Glu
NM_007194.4:c.1227C>G MANE Select	NP_009125.1:p.Asp409Glu
XM_006724114.3:c.780C>G	XP_006724177.2:p.Asp260Glu
XM_011529839.2:c.1386C>G	XP_011528141.1:p.Asp462Glu
XM_011529840.3:c.1299C>G	XP_011528142.1:p.Asp433Glu
XM_011529842.2:c.1056C>G	XP_011528144.1:p.Asp352Glu
XM_011529845.2:c.564C>G	XP_011528147.1:p.Asp188Glu
XM_017028560.1:c.1350C>G	XP_016884049.1:p.Asp450Glu
XM_017028561.2:c.564C>G	XP_016884050.1:p.Asp188Glu
XM_024452148.1:c.1257C>G	XP_024307916.1:p.Asp419Glu
XM_024452149.1:c.1170C>G	XP_024307917.1:p.Asp390Glu
XR_937805.2:n.1397C>G
NM_001005735.2:c.1356C>G	NP_001005735.1:p.Asp452Glu
NM_001257387.2:c.564C>G	NP_001244316.1:p.Asp188Glu
NM_001349956.2:c.1026C>G	NP_001336885.1:p.Asp342Glu