Canonical Allele Identifier: CA638798402

Gene: CHEK2

Linked Data

• dbSNP Id: rs1394994881
• gnomAD v2: 22-29092999-C-T
• gnomAD v4: 22-28697011-C-T
• MyVariant Identifiers: chr22:g.29092999C>T (hg19) ; chr22:g.28697011C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.28697011C>T , CM000684.2:g.28697011C>T	GRCh38
NC_000022.10:g.29092999C>T , CM000684.1:g.29092999C>T	GRCh37
NC_000022.9:g.27422999C>T	NCBI36
NG_008150.1:g.49824G>A
NG_008150.2:g.49856G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711048.1:c.1009-1769G>A	ENSP00000518557.1:n.1009-1769G>A
ENST00000402731.6:c.808-24G>A	ENSP00000384835.2:n.808-24G>A
ENST00000404276.6:c.1009-24G>A MANE Select	ENSP00000385747.1:n.1009-24G>A
ENST00000425190.7:c.346-24G>A	ENSP00000390244.2:n.346-24G>A
ENST00000464581.6:c.349-24G>A	ENSP00000483777.2:n.349-24G>A
ENST00000648295.1:n.561-24G>A
ENST00000649563.1:c.346-24G>A	ENSP00000496928.1:n.346-24G>A
ENST00000650281.1:c.1009-24G>A	ENSP00000497000.1:n.1009-24G>A
ENST00000328354.10:c.1009-24G>A	ENSP00000329178.6:n.1009-24G>A
ENST00000348295.7:c.1009-1138G>A	ENSP00000329012.5:n.1009-1138G>A
ENST00000382580.6:c.1138-24G>A	ENSP00000372023.2:n.1138-24G>A
ENST00000402731.5:c.1009-1138G>A	ENSP00000384835.1:n.1009-1138G>A
ENST00000403642.5:c.736-24G>A	ENSP00000384919.1:n.736-24G>A
ENST00000404276.5:c.1009-24G>A	ENSP00000385747.1:n.1009-24G>A
ENST00000405598.5:c.1009-24G>A	ENSP00000386087.1:n.1009-24G>A
ENST00000416671.5:c.*499-24G>A	ENSP00000402225.1:n.*499-24G>A
ENST00000417588.5:c.918-24G>A	ENSP00000412901.1:n.918-24G>A
ENST00000425190.6:c.346-24G>A	ENSP00000390244.1:n.346-24G>A
ENST00000433028.6:c.*734-24G>A	ENSP00000403659.1:n.*734-24G>A
ENST00000433728.5:c.947-24G>A	ENSP00000404400.1:n.947-24G>A
ENST00000434810.5:c.240-24G>A
ENST00000447421.5:c.808-24G>A	ENSP00000397478.2:n.808-24G>A
ENST00000448511.5:c.899-24G>A	ENSP00000404567.1:n.899-24G>A
ENST00000456369.5:c.263+2827G>A
ENST00000464581.5:c.349-24G>A	ENSP00000483777.1:n.349-24G>A
ENST00000491919.5:n.566-24G>A
NM_001005735.1:c.1138-24G>A	NP_001005735.1:n.1138-24G>A
NM_001257387.1:c.346-24G>A	NP_001244316.1:n.346-24G>A
NM_007194.3:c.1009-24G>A	NP_009125.1:n.1009-24G>A
NM_145862.2:c.1009-1138G>A	NP_665861.1:n.1009-1138G>A
XM_006724114.2:c.529-24G>A	XP_006724177.1:n.529-24G>A
XM_006724116.2:c.466-24G>A	XP_006724179.2:n.466-24G>A
XM_011529839.1:c.1168-24G>A	XP_011528141.1:n.1168-24G>A
XM_011529840.1:c.1168-1138G>A	XP_011528142.1:n.1168-1138G>A
XM_011529841.1:c.937-24G>A	XP_011528143.1:n.937-24G>A
XM_011529842.1:c.838-24G>A	XP_011528144.1:n.838-24G>A
XM_011529843.1:c.808-24G>A	XP_011528145.1:n.808-24G>A
XM_011529844.1:c.*56G>A	XP_011528146.1:n.*56G>A
XM_011529845.1:c.346-24G>A	XP_011528147.1:n.346-24G>A
XR_937805.1:n.1168-24G>A
XR_937806.1:n.1163-1138G>A
NM_001349956.1:c.808-24G>A	NP_001336885.1:n.808-24G>A
NM_007194.4:c.1009-24G>A MANE Select	NP_009125.1:n.1009-24G>A
XM_006724114.3:c.562-24G>A	XP_006724177.2:n.562-24G>A
XM_011529839.2:c.1168-24G>A	XP_011528141.1:n.1168-24G>A
XM_011529840.3:c.1168-1138G>A	XP_011528142.1:n.1168-1138G>A
XM_011529842.2:c.838-24G>A	XP_011528144.1:n.838-24G>A
XM_011529844.2:c.*56G>A	XP_011528146.1:n.*56G>A
XM_011529845.2:c.346-24G>A	XP_011528147.1:n.346-24G>A
XM_017028560.1:c.1132-24G>A	XP_016884049.1:n.1132-24G>A
XM_017028561.2:c.346-24G>A	XP_016884050.1:n.346-24G>A
XM_024452148.1:c.1039-24G>A	XP_024307916.1:n.1039-24G>A
XM_024452149.1:c.1039-1138G>A	XP_024307917.1:n.1039-1138G>A
XR_937805.2:n.1179-24G>A
XR_937806.2:n.1179-1138G>A
NM_001005735.2:c.1138-24G>A	NP_001005735.1:n.1138-24G>A
NM_001257387.2:c.346-24G>A	NP_001244316.1:n.346-24G>A
NM_001349956.2:c.808-24G>A	NP_001336885.1:n.808-24G>A