Canonical Allele Identifier: CA411099453

Gene: CHEK2

Linked Data

• ClinVar Variation Id: 483395
• ClinVar RCV Id: RCV003607321
• dbSNP Id: rs1555915357
• gnomAD v4: 22-28699855-T-C
• MyVariant Identifiers: chr22:g.29095843T>C (hg19) ; chr22:g.28699855T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.28699855T>C , CM000684.2:g.28699855T>C	GRCh38
NC_000022.10:g.29095843T>C , CM000684.1:g.29095843T>C	GRCh37
NC_000022.9:g.27425843T>C	NCBI36
NG_008150.1:g.46980A>G
NG_008150.2:g.47012A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000439346.6:c.900A>G	ENSP00000396903.2:n.900A>G
ENST00000711048.1:c.991A>G	ENSP00000518557.1:p.Met331Val
ENST00000402731.6:c.790A>G	ENSP00000384835.2:p.Met264Val
ENST00000404276.6:c.991A>G MANE Select	ENSP00000385747.1:p.Met331Val
ENST00000425190.7:c.328A>G	ENSP00000390244.2:p.Met110Val
ENST00000464581.6:c.331A>G	ENSP00000483777.2:p.Met111Val
ENST00000648295.1:n.543A>G
ENST00000649563.1:c.328A>G	ENSP00000496928.1:p.Met110Val
ENST00000650281.1:c.991A>G	ENSP00000497000.1:p.Met331Val
ENST00000328354.10:c.991A>G	ENSP00000329178.6:p.Met331Val
ENST00000348295.7:c.991A>G	ENSP00000329012.5:p.Met331Val
ENST00000382580.6:c.1120A>G	ENSP00000372023.2:p.Met374Val
ENST00000402731.5:c.991A>G	ENSP00000384835.1:p.Met331Val
ENST00000403642.5:c.718A>G	ENSP00000384919.1:p.Met240Val
ENST00000404276.5:c.991A>G	ENSP00000385747.1:p.Met331Val
ENST00000405598.5:c.991A>G	ENSP00000386087.1:p.Met331Val
ENST00000416671.5:c.*481A>G	ENSP00000402225.1:n.*481A>G
ENST00000417588.5:c.900A>G	ENSP00000412901.1:n.900A>G
ENST00000425190.6:c.328A>G	ENSP00000390244.1:p.Met110Val
ENST00000433028.6:c.*716A>G	ENSP00000403659.1:n.*716A>G
ENST00000433728.5:c.929A>G	ENSP00000404400.1:n.929A>G
ENST00000434810.5:c.222A>G
ENST00000439346.5:c.462A>G	ENSP00000396903.1:n.462A>G
ENST00000447421.5:c.790A>G	ENSP00000397478.2:p.Met264Val
ENST00000448511.5:c.881A>G	ENSP00000404567.1:n.881A>G
ENST00000456369.5:c.246A>G
ENST00000464581.5:c.331A>G	ENSP00000483777.1:p.Met111Val
ENST00000491919.5:n.548A>G
NM_001005735.1:c.1120A>G	NP_001005735.1:p.Met374Val
NM_001257387.1:c.328A>G	NP_001244316.1:p.Met110Val
NM_007194.3:c.991A>G	NP_009125.1:p.Met331Val
NM_145862.2:c.991A>G	NP_665861.1:p.Met331Val
XM_006724114.2:c.511A>G	XP_006724177.1:p.Met171Val
XM_006724116.2:c.448A>G	XP_006724179.2:p.Met150Val
XM_011529839.1:c.1150A>G	XP_011528141.1:p.Met384Val
XM_011529840.1:c.1150A>G	XP_011528142.1:p.Met384Val
XM_011529841.1:c.919A>G	XP_011528143.1:p.Met307Val
XM_011529842.1:c.820A>G	XP_011528144.1:p.Met274Val
XM_011529843.1:c.790A>G	XP_011528145.1:p.Met264Val
XM_011529844.1:c.1150A>G	XP_011528146.1:p.Met384Val
XM_011529845.1:c.328A>G	XP_011528147.1:p.Met110Val
XR_937805.1:n.1150A>G
XR_937806.1:n.1145A>G
XR_937807.1:n.1145A>G
NM_001349956.1:c.790A>G	NP_001336885.1:p.Met264Val
NM_007194.4:c.991A>G MANE Select	NP_009125.1:p.Met331Val
XM_006724114.3:c.544A>G	XP_006724177.2:p.Met182Val
XM_011529839.2:c.1150A>G	XP_011528141.1:p.Met384Val
XM_011529840.3:c.1150A>G	XP_011528142.1:p.Met384Val
XM_011529842.2:c.820A>G	XP_011528144.1:p.Met274Val
XM_011529844.2:c.1150A>G	XP_011528146.1:p.Met384Val
XM_011529845.2:c.328A>G	XP_011528147.1:p.Met110Val
XM_017028560.1:c.1114A>G	XP_016884049.1:p.Met372Val
XM_017028561.2:c.328A>G	XP_016884050.1:p.Met110Val
XM_024452148.1:c.1021A>G	XP_024307916.1:p.Met341Val
XM_024452149.1:c.1021A>G	XP_024307917.1:p.Met341Val
XR_937805.2:n.1161A>G
XR_937806.2:n.1161A>G
XR_937807.2:n.1161A>G
NM_001005735.2:c.1120A>G	NP_001005735.1:p.Met374Val
NM_001257387.2:c.328A>G	NP_001244316.1:p.Met110Val
NM_001349956.2:c.790A>G	NP_001336885.1:p.Met264Val