Canonical Allele Identifier: CA2737851234

Gene: CHEK2

Linked Data

• dbSNP Id: rs61611714

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.28690955dup , CM000684.2:g.28690955dup	GRCh38
NC_000022.10:g.29086943dup , CM000684.1:g.29086943dup	GRCh37
NC_000022.9:g.27416943dup	NCBI36
NG_008150.1:g.55882dup
NG_008150.2:g.55914dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000711048.1:c.*197-1738dup	ENSP00000518557.1:n.*197-1738dup
ENST00000402731.6:c.1261-1738dup	ENSP00000384835.2:n.1261-1738dup
ENST00000404276.6:c.1462-1738dup MANE Select	ENSP00000385747.1:n.1462-1738dup
ENST00000425190.7:c.799-1738dup	ENSP00000390244.2:n.799-1738dup
ENST00000464581.6:c.802-1738dup	ENSP00000483777.2:n.802-1738dup
ENST00000648295.1:n.1014-1738dup
ENST00000649563.1:c.799-1738dup	ENSP00000496928.1:n.799-1738dup
ENST00000650281.1:c.1462-1738dup	ENSP00000497000.1:n.1462-1738dup
ENST00000328354.10:c.1462-1738dup	ENSP00000329178.6:n.1462-1738dup
ENST00000348295.7:c.1375-1738dup	ENSP00000329012.5:n.1375-1738dup
ENST00000382580.6:c.1591-1738dup	ENSP00000372023.2:n.1591-1738dup
ENST00000402731.5:c.1375-1738dup	ENSP00000384835.1:n.1375-1738dup
ENST00000403642.5:c.1189-1738dup	ENSP00000384919.1:n.1189-1738dup
ENST00000404276.5:c.1462-1738dup	ENSP00000385747.1:n.1462-1738dup
ENST00000405598.5:c.1462-1738dup	ENSP00000386087.1:n.1462-1738dup
ENST00000416671.5:c.*952-1738dup	ENSP00000402225.1:n.*952-1738dup
ENST00000417588.5:c.1371-1738dup	ENSP00000412901.1:n.1371-1738dup
ENST00000433728.5:c.1400-1738dup	ENSP00000404400.1:n.1400-1738dup
ENST00000434810.5:c.660-1738dup
ENST00000448511.5:c.1352-1738dup	ENSP00000404567.1:n.1352-1738dup
ENST00000456369.5:c.264-1738dup
NM_001005735.1:c.1591-1738dup	NP_001005735.1:n.1591-1738dup
NM_001257387.1:c.799-1738dup	NP_001244316.1:n.799-1738dup
NM_007194.3:c.1462-1738dup	NP_009125.1:n.1462-1738dup
NM_145862.2:c.1375-1738dup	NP_665861.1:n.1375-1738dup
XM_006724114.2:c.982-1738dup	XP_006724177.1:n.982-1738dup
XM_006724116.2:c.919-1738dup	XP_006724179.2:n.919-1738dup
XM_011529839.1:c.1621-1738dup	XP_011528141.1:n.1621-1738dup
XM_011529840.1:c.1534-1738dup	XP_011528142.1:n.1534-1738dup
XM_011529841.1:c.1390-1738dup	XP_011528143.1:n.1390-1738dup
XM_011529842.1:c.1291-1738dup	XP_011528144.1:n.1291-1738dup
XM_011529843.1:c.1261-1738dup	XP_011528145.1:n.1261-1738dup
XM_011529845.1:c.799-1738dup	XP_011528147.1:n.799-1738dup
XR_937805.1:n.1621-1738dup
NM_001349956.1:c.1261-1738dup	NP_001336885.1:n.1261-1738dup
NM_007194.4:c.1462-1738dup MANE Select	NP_009125.1:n.1462-1738dup
XM_006724114.3:c.1015-1738dup	XP_006724177.2:n.1015-1738dup
XM_011529839.2:c.1621-1738dup	XP_011528141.1:n.1621-1738dup
XM_011529840.3:c.1534-1738dup	XP_011528142.1:n.1534-1738dup
XM_011529842.2:c.1291-1738dup	XP_011528144.1:n.1291-1738dup
XM_011529845.2:c.799-1738dup	XP_011528147.1:n.799-1738dup
XM_017028560.1:c.1585-1738dup	XP_016884049.1:n.1585-1738dup
XM_017028561.2:c.799-1738dup	XP_016884050.1:n.799-1738dup
XM_024452148.1:c.1492-1738dup	XP_024307916.1:n.1492-1738dup
XM_024452149.1:c.1405-1738dup	XP_024307917.1:n.1405-1738dup
XR_937805.2:n.1632-1738dup
NM_001005735.2:c.1591-1738dup	NP_001005735.1:n.1591-1738dup
NM_001257387.2:c.799-1738dup	NP_001244316.1:n.799-1738dup
NM_001349956.2:c.1261-1738dup	NP_001336885.1:n.1261-1738dup