Canonical Allele Identifier: CA2737970152

Gene: CHEK2

Linked Data

• dbSNP Id: rs2145808457

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.28695942A>T , CM000684.2:g.28695942A>T	GRCh38
NC_000022.10:g.29091930A>T , CM000684.1:g.29091930A>T	GRCh37
NC_000022.9:g.27421930A>T	NCBI36
NG_008150.1:g.50893T>A
NG_008150.2:g.50925T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711048.1:c.1009-700T>A	ENSP00000518557.1:n.1009-700T>A
ENST00000402731.6:c.895-69T>A	ENSP00000384835.2:n.895-69T>A
ENST00000404276.6:c.1096-69T>A MANE Select	ENSP00000385747.1:n.1096-69T>A
ENST00000425190.7:c.433-69T>A	ENSP00000390244.2:n.433-69T>A
ENST00000464581.6:c.436-69T>A	ENSP00000483777.2:n.436-69T>A
ENST00000648295.1:n.648-69T>A
ENST00000649563.1:c.433-69T>A	ENSP00000496928.1:n.433-69T>A
ENST00000650281.1:c.1096-69T>A	ENSP00000497000.1:n.1096-69T>A
ENST00000328354.10:c.1096-69T>A	ENSP00000329178.6:n.1096-69T>A
ENST00000348295.7:c.1009-69T>A	ENSP00000329012.5:n.1009-69T>A
ENST00000382580.6:c.1225-69T>A	ENSP00000372023.2:n.1225-69T>A
ENST00000402731.5:c.1009-69T>A	ENSP00000384835.1:n.1009-69T>A
ENST00000403642.5:c.823-69T>A	ENSP00000384919.1:n.823-69T>A
ENST00000404276.5:c.1096-69T>A	ENSP00000385747.1:n.1096-69T>A
ENST00000405598.5:c.1096-69T>A	ENSP00000386087.1:n.1096-69T>A
ENST00000416671.5:c.*586-69T>A	ENSP00000402225.1:n.*586-69T>A
ENST00000417588.5:c.1005-69T>A	ENSP00000412901.1:n.1005-69T>A
ENST00000433728.5:c.1034-69T>A	ENSP00000404400.1:n.1034-69T>A
ENST00000434810.5:c.327-69T>A
ENST00000448511.5:c.986-69T>A	ENSP00000404567.1:n.986-69T>A
ENST00000456369.5:c.263+3896T>A
NM_001005735.1:c.1225-69T>A	NP_001005735.1:n.1225-69T>A
NM_001257387.1:c.433-69T>A	NP_001244316.1:n.433-69T>A
NM_007194.3:c.1096-69T>A	NP_009125.1:n.1096-69T>A
NM_145862.2:c.1009-69T>A	NP_665861.1:n.1009-69T>A
XM_006724114.2:c.616-69T>A	XP_006724177.1:n.616-69T>A
XM_006724116.2:c.553-69T>A	XP_006724179.2:n.553-69T>A
XM_011529839.1:c.1255-69T>A	XP_011528141.1:n.1255-69T>A
XM_011529840.1:c.1168-69T>A	XP_011528142.1:n.1168-69T>A
XM_011529841.1:c.1024-69T>A	XP_011528143.1:n.1024-69T>A
XM_011529842.1:c.925-69T>A	XP_011528144.1:n.925-69T>A
XM_011529843.1:c.895-69T>A	XP_011528145.1:n.895-69T>A
XM_011529845.1:c.433-69T>A	XP_011528147.1:n.433-69T>A
XR_937805.1:n.1255-69T>A
XR_937806.1:n.1163-69T>A
NM_001349956.1:c.895-69T>A	NP_001336885.1:n.895-69T>A
NM_007194.4:c.1096-69T>A MANE Select	NP_009125.1:n.1096-69T>A
XM_006724114.3:c.649-69T>A	XP_006724177.2:n.649-69T>A
XM_011529839.2:c.1255-69T>A	XP_011528141.1:n.1255-69T>A
XM_011529840.3:c.1168-69T>A	XP_011528142.1:n.1168-69T>A
XM_011529842.2:c.925-69T>A	XP_011528144.1:n.925-69T>A
XM_011529845.2:c.433-69T>A	XP_011528147.1:n.433-69T>A
XM_017028560.1:c.1219-69T>A	XP_016884049.1:n.1219-69T>A
XM_017028561.2:c.433-69T>A	XP_016884050.1:n.433-69T>A
XM_024452148.1:c.1126-69T>A	XP_024307916.1:n.1126-69T>A
XM_024452149.1:c.1039-69T>A	XP_024307917.1:n.1039-69T>A
XR_937805.2:n.1266-69T>A
XR_937806.2:n.1179-69T>A
NM_001005735.2:c.1225-69T>A	NP_001005735.1:n.1225-69T>A
NM_001257387.2:c.433-69T>A	NP_001244316.1:n.433-69T>A
NM_001349956.2:c.895-69T>A	NP_001336885.1:n.895-69T>A