Canonical Allele Identifier: CA752164254
Gene: CHEK2 HGNC NCBI

Linked Data

dbSNP Id: rs1186180086

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.28693857T>C , CM000684.2:g.28693857T>C GRCh38
NC_000022.10:g.29089845T>C , CM000684.1:g.29089845T>C GRCh37
NC_000022.9:g.27419845T>C NCBI36
NG_008150.1:g.52978A>G
NG_008150.2:g.53010A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000711048.1:c.*196+175A>G ENSP00000518557.1:n.*196+175A>G
ENST00000402731.6:c.1260+175A>G ENSP00000384835.2:n.1260+175A>G
ENST00000404276.6:c.1461+175A>G MANE Select ENSP00000385747.1:n.1461+175A>G
ENST00000425190.7:c.798+175A>G ENSP00000390244.2:n.798+175A>G
ENST00000464581.6:c.801+175A>G ENSP00000483777.2:n.801+175A>G
ENST00000648295.1:n.1013+175A>G
ENST00000649563.1:c.798+175A>G ENSP00000496928.1:n.798+175A>G
ENST00000650281.1:c.1461+175A>G ENSP00000497000.1:n.1461+175A>G
ENST00000328354.10:c.1461+175A>G ENSP00000329178.6:n.1461+175A>G
ENST00000348295.7:c.1374+175A>G ENSP00000329012.5:n.1374+175A>G
ENST00000382580.6:c.1590+175A>G ENSP00000372023.2:n.1590+175A>G
ENST00000402731.5:c.1374+175A>G ENSP00000384835.1:n.1374+175A>G
ENST00000403642.5:c.1188+175A>G ENSP00000384919.1:n.1188+175A>G
ENST00000404276.5:c.1461+175A>G ENSP00000385747.1:n.1461+175A>G
ENST00000405598.5:c.1461+175A>G ENSP00000386087.1:n.1461+175A>G
ENST00000416671.5:c.*951+175A>G ENSP00000402225.1:n.*951+175A>G
ENST00000417588.5:c.1370+175A>G ENSP00000412901.1:n.1370+175A>G
ENST00000433728.5:c.1399+175A>G ENSP00000404400.1:n.1399+175A>G
ENST00000434810.5:c.659+175A>G
ENST00000448511.5:c.1351+175A>G ENSP00000404567.1:n.1351+175A>G
ENST00000456369.5:c.264-4642A>G
NM_001005735.1:c.1590+175A>G NP_001005735.1:n.1590+175A>G
NM_001257387.1:c.798+175A>G NP_001244316.1:n.798+175A>G
NM_007194.3:c.1461+175A>G NP_009125.1:n.1461+175A>G
NM_145862.2:c.1374+175A>G NP_665861.1:n.1374+175A>G
XM_006724114.2:c.981+175A>G XP_006724177.1:n.981+175A>G
XM_006724116.2:c.918+175A>G XP_006724179.2:n.918+175A>G
XM_011529839.1:c.1620+175A>G XP_011528141.1:n.1620+175A>G
XM_011529840.1:c.1533+175A>G XP_011528142.1:n.1533+175A>G
XM_011529841.1:c.1389+175A>G XP_011528143.1:n.1389+175A>G
XM_011529842.1:c.1290+175A>G XP_011528144.1:n.1290+175A>G
XM_011529843.1:c.1260+175A>G XP_011528145.1:n.1260+175A>G
XM_011529845.1:c.798+175A>G XP_011528147.1:n.798+175A>G
XR_937805.1:n.1620+175A>G
NM_001349956.1:c.1260+175A>G NP_001336885.1:n.1260+175A>G
NM_007194.4:c.1461+175A>G MANE Select NP_009125.1:n.1461+175A>G
XM_006724114.3:c.1014+175A>G XP_006724177.2:n.1014+175A>G
XM_011529839.2:c.1620+175A>G XP_011528141.1:n.1620+175A>G
XM_011529840.3:c.1533+175A>G XP_011528142.1:n.1533+175A>G
XM_011529842.2:c.1290+175A>G XP_011528144.1:n.1290+175A>G
XM_011529845.2:c.798+175A>G XP_011528147.1:n.798+175A>G
XM_017028560.1:c.1584+175A>G XP_016884049.1:n.1584+175A>G
XM_017028561.2:c.798+175A>G XP_016884050.1:n.798+175A>G
XM_024452148.1:c.1491+175A>G XP_024307916.1:n.1491+175A>G
XM_024452149.1:c.1404+175A>G XP_024307917.1:n.1404+175A>G
XR_937805.2:n.1631+175A>G
NM_001005735.2:c.1590+175A>G NP_001005735.1:n.1590+175A>G
NM_001257387.2:c.798+175A>G NP_001244316.1:n.798+175A>G
NM_001349956.2:c.1260+175A>G NP_001336885.1:n.1260+175A>G