Canonical Allele Identifier: CA2655953180

Gene: CHEK2

Linked Data

• gnomAD v4: 22-28697132-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.28697134del , CM000684.2:g.28697134del	GRCh38
NC_000022.10:g.29093122del , CM000684.1:g.29093122del	GRCh37
NC_000022.9:g.27423122del	NCBI36
NG_008150.1:g.49702del
NG_008150.2:g.49734del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711048.1:c.1009-1891del	ENSP00000518557.1:n.1009-1891del
ENST00000402731.6:c.808-146del	ENSP00000384835.2:n.808-146del
ENST00000404276.6:c.1009-146del MANE Select	ENSP00000385747.1:n.1009-146del
ENST00000425190.7:c.346-146del	ENSP00000390244.2:n.346-146del
ENST00000464581.6:c.349-146del	ENSP00000483777.2:n.349-146del
ENST00000648295.1:n.561-146del
ENST00000649563.1:c.346-146del	ENSP00000496928.1:n.346-146del
ENST00000650281.1:c.1009-146del	ENSP00000497000.1:n.1009-146del
ENST00000328354.10:c.1009-146del	ENSP00000329178.6:n.1009-146del
ENST00000348295.7:c.1009-1260del	ENSP00000329012.5:n.1009-1260del
ENST00000382580.6:c.1138-146del	ENSP00000372023.2:n.1138-146del
ENST00000402731.5:c.1009-1260del	ENSP00000384835.1:n.1009-1260del
ENST00000403642.5:c.736-146del	ENSP00000384919.1:n.736-146del
ENST00000404276.5:c.1009-146del	ENSP00000385747.1:n.1009-146del
ENST00000405598.5:c.1009-146del	ENSP00000386087.1:n.1009-146del
ENST00000416671.5:c.*499-146del	ENSP00000402225.1:n.*499-146del
ENST00000417588.5:c.918-146del	ENSP00000412901.1:n.918-146del
ENST00000425190.6:c.346-146del	ENSP00000390244.1:n.346-146del
ENST00000433028.6:c.*734-146del	ENSP00000403659.1:n.*734-146del
ENST00000433728.5:c.947-146del	ENSP00000404400.1:n.947-146del
ENST00000434810.5:c.240-146del
ENST00000447421.5:c.808-146del	ENSP00000397478.2:n.808-146del
ENST00000448511.5:c.899-146del	ENSP00000404567.1:n.899-146del
ENST00000456369.5:c.263+2705del
ENST00000464581.5:c.349-146del	ENSP00000483777.1:n.349-146del
ENST00000491919.5:n.566-146del
NM_001005735.1:c.1138-146del	NP_001005735.1:n.1138-146del
NM_001257387.1:c.346-146del	NP_001244316.1:n.346-146del
NM_007194.3:c.1009-146del	NP_009125.1:n.1009-146del
NM_145862.2:c.1009-1260del	NP_665861.1:n.1009-1260del
XM_006724114.2:c.529-146del	XP_006724177.1:n.529-146del
XM_006724116.2:c.466-146del	XP_006724179.2:n.466-146del
XM_011529839.1:c.1168-146del	XP_011528141.1:n.1168-146del
XM_011529840.1:c.1168-1260del	XP_011528142.1:n.1168-1260del
XM_011529841.1:c.937-146del	XP_011528143.1:n.937-146del
XM_011529842.1:c.838-146del	XP_011528144.1:n.838-146del
XM_011529843.1:c.808-146del	XP_011528145.1:n.808-146del
XM_011529844.1:c.1168-4del	XP_011528146.1:n.1168-4del
XM_011529845.1:c.346-146del	XP_011528147.1:n.346-146del
XR_937805.1:n.1168-146del
XR_937806.1:n.1163-1260del
XR_937807.1:n.1163-4del
NM_001349956.1:c.808-146del	NP_001336885.1:n.808-146del
NM_007194.4:c.1009-146del MANE Select	NP_009125.1:n.1009-146del
XM_006724114.3:c.562-146del	XP_006724177.2:n.562-146del
XM_011529839.2:c.1168-146del	XP_011528141.1:n.1168-146del
XM_011529840.3:c.1168-1260del	XP_011528142.1:n.1168-1260del
XM_011529842.2:c.838-146del	XP_011528144.1:n.838-146del
XM_011529844.2:c.1168-4del	XP_011528146.1:n.1168-4del
XM_011529845.2:c.346-146del	XP_011528147.1:n.346-146del
XM_017028560.1:c.1132-146del	XP_016884049.1:n.1132-146del
XM_017028561.2:c.346-146del	XP_016884050.1:n.346-146del
XM_024452148.1:c.1039-146del	XP_024307916.1:n.1039-146del
XM_024452149.1:c.1039-1260del	XP_024307917.1:n.1039-1260del
XR_937805.2:n.1179-146del
XR_937806.2:n.1179-1260del
XR_937807.2:n.1179-4del
NM_001005735.2:c.1138-146del	NP_001005735.1:n.1138-146del
NM_001257387.2:c.346-146del	NP_001244316.1:n.346-146del
NM_001349956.2:c.808-146del	NP_001336885.1:n.808-146del