Canonical Allele Identifier: CA513944921

Gene: CHEK2

Linked Data

• MyVariant Identifiers: chr22:g.29091799T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.28695811T>G , CM000684.2:g.28695811T>G	GRCh38
NC_000022.10:g.29091799T>G , CM000684.1:g.29091799T>G	GRCh37
NC_000022.9:g.27421799T>G	NCBI36
NG_008150.1:g.51024A>C
NG_008150.2:g.51056A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711048.1:c.1009-569A>C	ENSP00000518557.1:n.1009-569A>C
ENST00000402731.6:c.957A>C	ENSP00000384835.2:p.Gly319=
ENST00000404276.6:c.1158A>C MANE Select	ENSP00000385747.1:p.Gly386=
ENST00000425190.7:c.495A>C	ENSP00000390244.2:p.Gly165=
ENST00000464581.6:c.498A>C	ENSP00000483777.2:p.Gly166=
ENST00000648295.1:n.710A>C
ENST00000649563.1:c.495A>C	ENSP00000496928.1:p.Gly165=
ENST00000650281.1:c.1158A>C	ENSP00000497000.1:p.Gly386=
ENST00000328354.10:c.1158A>C	ENSP00000329178.6:p.Gly386=
ENST00000348295.7:c.1071A>C	ENSP00000329012.5:p.Gly357=
ENST00000382580.6:c.1287A>C	ENSP00000372023.2:p.Gly429=
ENST00000402731.5:c.1071A>C	ENSP00000384835.1:p.Gly357=
ENST00000403642.5:c.885A>C	ENSP00000384919.1:p.Gly295=
ENST00000404276.5:c.1158A>C	ENSP00000385747.1:p.Gly386=
ENST00000405598.5:c.1158A>C	ENSP00000386087.1:p.Gly386=
ENST00000416671.5:c.*648A>C	ENSP00000402225.1:n.*648A>C
ENST00000417588.5:c.1067A>C	ENSP00000412901.1:n.1067A>C
ENST00000433728.5:c.1096A>C	ENSP00000404400.1:n.1096A>C
ENST00000434810.5:c.389A>C
ENST00000448511.5:c.1048A>C	ENSP00000404567.1:n.1048A>C
ENST00000456369.5:c.263+4027A>C
NM_001005735.1:c.1287A>C	NP_001005735.1:p.Gly429=
NM_001257387.1:c.495A>C	NP_001244316.1:p.Gly165=
NM_007194.3:c.1158A>C	NP_009125.1:p.Gly386=
NM_145862.2:c.1071A>C	NP_665861.1:p.Gly357=
XM_006724114.2:c.678A>C	XP_006724177.1:p.Gly226=
XM_006724116.2:c.615A>C	XP_006724179.2:p.Gly205=
XM_011529839.1:c.1317A>C	XP_011528141.1:p.Gly439=
XM_011529840.1:c.1230A>C	XP_011528142.1:p.Gly410=
XM_011529841.1:c.1086A>C	XP_011528143.1:p.Gly362=
XM_011529842.1:c.987A>C	XP_011528144.1:p.Gly329=
XM_011529843.1:c.957A>C	XP_011528145.1:p.Gly319=
XM_011529845.1:c.495A>C	XP_011528147.1:p.Gly165=
XR_937805.1:n.1317A>C
XR_937806.1:n.1225A>C
NM_001349956.1:c.957A>C	NP_001336885.1:p.Gly319=
NM_007194.4:c.1158A>C MANE Select	NP_009125.1:p.Gly386=
XM_006724114.3:c.711A>C	XP_006724177.2:p.Gly237=
XM_011529839.2:c.1317A>C	XP_011528141.1:p.Gly439=
XM_011529840.3:c.1230A>C	XP_011528142.1:p.Gly410=
XM_011529842.2:c.987A>C	XP_011528144.1:p.Gly329=
XM_011529845.2:c.495A>C	XP_011528147.1:p.Gly165=
XM_017028560.1:c.1281A>C	XP_016884049.1:p.Gly427=
XM_017028561.2:c.495A>C	XP_016884050.1:p.Gly165=
XM_024452148.1:c.1188A>C	XP_024307916.1:p.Gly396=
XM_024452149.1:c.1101A>C	XP_024307917.1:p.Gly367=
XR_937805.2:n.1328A>C
XR_937806.2:n.1241A>C
NM_001005735.2:c.1287A>C	NP_001005735.1:p.Gly429=
NM_001257387.2:c.495A>C	NP_001244316.1:p.Gly165=
NM_001349956.2:c.957A>C	NP_001336885.1:p.Gly319=