Canonical Allele Identifier: CA411097802

Gene: CHEK2

Linked Data

• MyVariant Identifiers: chr22:g.29092964T>G (hg19) ; chr22:g.28696976T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.28696976T>G , CM000684.2:g.28696976T>G	GRCh38
NC_000022.10:g.29092964T>G , CM000684.1:g.29092964T>G	GRCh37
NC_000022.9:g.27422964T>G	NCBI36
NG_008150.1:g.49859A>C
NG_008150.2:g.49891A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711048.1:c.1009-1734A>C	ENSP00000518557.1:n.1009-1734A>C
ENST00000402731.6:c.819A>C	ENSP00000384835.2:p.Glu273Asp
ENST00000404276.6:c.1020A>C MANE Select	ENSP00000385747.1:p.Glu340Asp
ENST00000425190.7:c.357A>C	ENSP00000390244.2:p.Glu119Asp
ENST00000464581.6:c.360A>C	ENSP00000483777.2:p.Glu120Asp
ENST00000648295.1:n.572A>C
ENST00000649563.1:c.357A>C	ENSP00000496928.1:p.Glu119Asp
ENST00000650281.1:c.1020A>C	ENSP00000497000.1:p.Glu340Asp
ENST00000328354.10:c.1020A>C	ENSP00000329178.6:p.Glu340Asp
ENST00000348295.7:c.1009-1103A>C	ENSP00000329012.5:n.1009-1103A>C
ENST00000382580.6:c.1149A>C	ENSP00000372023.2:p.Glu383Asp
ENST00000402731.5:c.1009-1103A>C	ENSP00000384835.1:n.1009-1103A>C
ENST00000403642.5:c.747A>C	ENSP00000384919.1:p.Glu249Asp
ENST00000404276.5:c.1020A>C	ENSP00000385747.1:p.Glu340Asp
ENST00000405598.5:c.1020A>C	ENSP00000386087.1:p.Glu340Asp
ENST00000416671.5:c.*510A>C	ENSP00000402225.1:n.*510A>C
ENST00000417588.5:c.929A>C	ENSP00000412901.1:n.929A>C
ENST00000425190.6:c.357A>C	ENSP00000390244.1:p.Glu119Asp
ENST00000433028.6:c.*745A>C	ENSP00000403659.1:n.*745A>C
ENST00000433728.5:c.958A>C	ENSP00000404400.1:n.958A>C
ENST00000434810.5:c.251A>C
ENST00000447421.5:c.819A>C	ENSP00000397478.2:p.Glu273Asp
ENST00000448511.5:c.910A>C	ENSP00000404567.1:n.910A>C
ENST00000456369.5:c.263+2862A>C
ENST00000464581.5:c.360A>C	ENSP00000483777.1:p.Glu120Asp
ENST00000491919.5:n.577A>C
NM_001005735.1:c.1149A>C	NP_001005735.1:p.Glu383Asp
NM_001257387.1:c.357A>C	NP_001244316.1:p.Glu119Asp
NM_007194.3:c.1020A>C	NP_009125.1:p.Glu340Asp
NM_145862.2:c.1009-1103A>C	NP_665861.1:n.1009-1103A>C
XM_006724114.2:c.540A>C	XP_006724177.1:p.Glu180Asp
XM_006724116.2:c.477A>C	XP_006724179.2:p.Glu159Asp
XM_011529839.1:c.1179A>C	XP_011528141.1:p.Glu393Asp
XM_011529840.1:c.1168-1103A>C	XP_011528142.1:n.1168-1103A>C
XM_011529841.1:c.948A>C	XP_011528143.1:p.Glu316Asp
XM_011529842.1:c.849A>C	XP_011528144.1:p.Glu283Asp
XM_011529843.1:c.819A>C	XP_011528145.1:p.Glu273Asp
XM_011529845.1:c.357A>C	XP_011528147.1:p.Glu119Asp
XR_937805.1:n.1179A>C
XR_937806.1:n.1163-1103A>C
NM_001349956.1:c.819A>C	NP_001336885.1:p.Glu273Asp
NM_007194.4:c.1020A>C MANE Select	NP_009125.1:p.Glu340Asp
XM_006724114.3:c.573A>C	XP_006724177.2:p.Glu191Asp
XM_011529839.2:c.1179A>C	XP_011528141.1:p.Glu393Asp
XM_011529840.3:c.1168-1103A>C	XP_011528142.1:n.1168-1103A>C
XM_011529842.2:c.849A>C	XP_011528144.1:p.Glu283Asp
XM_011529845.2:c.357A>C	XP_011528147.1:p.Glu119Asp
XM_017028560.1:c.1143A>C	XP_016884049.1:p.Glu381Asp
XM_017028561.2:c.357A>C	XP_016884050.1:p.Glu119Asp
XM_024452148.1:c.1050A>C	XP_024307916.1:p.Glu350Asp
XM_024452149.1:c.1039-1103A>C	XP_024307917.1:n.1039-1103A>C
XR_937805.2:n.1190A>C
XR_937806.2:n.1179-1103A>C
NM_001005735.2:c.1149A>C	NP_001005735.1:p.Glu383Asp
NM_001257387.2:c.357A>C	NP_001244316.1:p.Glu119Asp
NM_001349956.2:c.819A>C	NP_001336885.1:p.Glu273Asp