Canonical Allele Identifier: CA2400242624
Gene: CHEK2 HGNC NCBI

Linked Data

dbSNP Id: rs2053042273

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.28704751_28704752insAAC , CM000684.2:g.28704751_28704752insAAC GRCh38
NC_000022.10:g.29100739_29100740insAAC , CM000684.1:g.29100739_29100740insAAC GRCh37
NC_000022.9:g.27430739_27430740insAAC NCBI36
NG_008150.1:g.42083_42084insGTT
NG_008150.2:g.42115_42116insGTT

Transcript Alleles

HGVS Amino-acid change
ENST00000439346.6:c.756-1186_756-1185insGTT ENSP00000396903.2:n.756-1186_756-1185insG...
ENST00000711048.1:c.847-1186_847-1185insGTT ENSP00000518557.1:n.847-1186_847-1185insG...
ENST00000402731.6:c.646-1186_646-1185insGTT ENSP00000384835.2:n.646-1186_646-1185insG...
ENST00000404276.6:c.847-1186_847-1185insGTT MANE Select ENSP00000385747.1:n.847-1186_847-1185insG...
ENST00000425190.7:c.184-1186_184-1185insGTT ENSP00000390244.2:n.184-1186_184-1185insG...
ENST00000464581.6:c.187-1186_187-1185insGTT ENSP00000483777.2:n.187-1186_187-1185insG...
ENST00000648295.1:n.399-1186_399-1185insGTT
ENST00000649563.1:c.184-1186_184-1185insGTT ENSP00000496928.1:n.184-1186_184-1185insG...
ENST00000650281.1:c.847-1186_847-1185insGTT ENSP00000497000.1:n.847-1186_847-1185insG...
ENST00000328354.10:c.847-1186_847-1185insGTT ENSP00000329178.6:n.847-1186_847-1185insG...
ENST00000348295.7:c.847-1186_847-1185insGTT ENSP00000329012.5:n.847-1186_847-1185insG...
ENST00000382580.6:c.976-1186_976-1185insGTT ENSP00000372023.2:n.976-1186_976-1185insG...
ENST00000402731.5:c.847-1186_847-1185insGTT ENSP00000384835.1:n.847-1186_847-1185insG...
ENST00000403642.5:c.574-1186_574-1185insGTT ENSP00000384919.1:n.574-1186_574-1185insG...
ENST00000404276.5:c.847-1186_847-1185insGTT ENSP00000385747.1:n.847-1186_847-1185insG...
ENST00000405598.5:c.847-1186_847-1185insGTT ENSP00000386087.1:n.847-1186_847-1185insG...
ENST00000416671.5:c.*337-1186_*337-1185insGTT ENSP00000402225.1:n.*337-1186_*337-1185in...
ENST00000417588.5:c.756-1186_756-1185insGTT ENSP00000412901.1:n.756-1186_756-1185insG...
ENST00000425190.6:c.184-1186_184-1185insGTT ENSP00000390244.1:n.184-1186_184-1185insG...
ENST00000433028.6:c.*572-1186_*572-1185insGTT ENSP00000403659.1:n.*572-1186_*572-1185in...
ENST00000433728.5:c.847-4815_847-4814insGTT ENSP00000404400.1:n.847-4815_847-4814insG...
ENST00000434810.5:c.78-1186_78-1185insGTT
ENST00000439346.5:c.318-1186_318-1185insGTT ENSP00000396903.1:n.318-1186_318-1185insG...
ENST00000447421.5:c.646-1186_646-1185insGTT ENSP00000397478.2:n.646-1186_646-1185insG...
ENST00000448511.5:c.737-1186_737-1185insGTT ENSP00000404567.1:n.737-1186_737-1185insG...
ENST00000456369.5:c.102-1186_102-1185insGTT
ENST00000464581.5:c.187-1186_187-1185insGTT ENSP00000483777.1:n.187-1186_187-1185insG...
ENST00000491919.5:n.404-1186_404-1185insGTT
NM_001005735.1:c.976-1186_976-1185insGTT NP_001005735.1:n.976-1186_976-1185insGTT
NM_001257387.1:c.184-1186_184-1185insGTT NP_001244316.1:n.184-1186_184-1185insGTT
NM_007194.3:c.847-1186_847-1185insGTT NP_009125.1:n.847-1186_847-1185insGTT
NM_145862.2:c.847-1186_847-1185insGTT NP_665861.1:n.847-1186_847-1185insGTT
XM_006724114.2:c.367-1186_367-1185insGTT XP_006724177.1:n.367-1186_367-1185insGTT
XM_006724116.2:c.304-1186_304-1185insGTT XP_006724179.2:n.304-1186_304-1185insGTT
XM_011529839.1:c.1006-1186_1006-1185insGTT XP_011528141.1:n.1006-1186_1006-1185insGT...
XM_011529840.1:c.1006-1186_1006-1185insGTT XP_011528142.1:n.1006-1186_1006-1185insGT...
XM_011529841.1:c.775-1186_775-1185insGTT XP_011528143.1:n.775-1186_775-1185insGTT
XM_011529842.1:c.676-1186_676-1185insGTT XP_011528144.1:n.676-1186_676-1185insGTT
XM_011529843.1:c.646-1186_646-1185insGTT XP_011528145.1:n.646-1186_646-1185insGTT
XM_011529844.1:c.1006-1186_1006-1185insGTT XP_011528146.1:n.1006-1186_1006-1185insGT...
XM_011529845.1:c.184-1186_184-1185insGTT XP_011528147.1:n.184-1186_184-1185insGTT
XR_937805.1:n.1068-4815_1068-4814insGTT
XR_937806.1:n.1063-4815_1063-4814insGTT
XR_937807.1:n.1063-4815_1063-4814insGTT
NM_001349956.1:c.646-1186_646-1185insGTT NP_001336885.1:n.646-1186_646-1185insGTT
NM_007194.4:c.847-1186_847-1185insGTT MANE Select NP_009125.1:n.847-1186_847-1185insGTT
XM_006724114.3:c.400-1186_400-1185insGTT XP_006724177.2:n.400-1186_400-1185insGTT
XM_011529839.2:c.1006-1186_1006-1185insGTT XP_011528141.1:n.1006-1186_1006-1185insGT...
XM_011529840.3:c.1006-1186_1006-1185insGTT XP_011528142.1:n.1006-1186_1006-1185insGT...
XM_011529842.2:c.676-1186_676-1185insGTT XP_011528144.1:n.676-1186_676-1185insGTT
XM_011529844.2:c.1006-1186_1006-1185insGTT XP_011528146.1:n.1006-1186_1006-1185insGT...
XM_011529845.2:c.184-1186_184-1185insGTT XP_011528147.1:n.184-1186_184-1185insGTT
XM_017028560.1:c.970-1186_970-1185insGTT XP_016884049.1:n.970-1186_970-1185insGTT
XM_017028561.2:c.184-1186_184-1185insGTT XP_016884050.1:n.184-1186_184-1185insGTT
XM_024452148.1:c.877-1186_877-1185insGTT XP_024307916.1:n.877-1186_877-1185insGTT
XM_024452149.1:c.877-1186_877-1185insGTT XP_024307917.1:n.877-1186_877-1185insGTT
XR_937805.2:n.1079-4815_1079-4814insGTT
XR_937806.2:n.1079-4815_1079-4814insGTT
XR_937807.2:n.1079-4815_1079-4814insGTT
NM_001005735.2:c.976-1186_976-1185insGTT NP_001005735.1:n.976-1186_976-1185insGTT
NM_001257387.2:c.184-1186_184-1185insGTT NP_001244316.1:n.184-1186_184-1185insGTT
NM_001349956.2:c.646-1186_646-1185insGTT NP_001336885.1:n.646-1186_646-1185insGTT