Canonical Allele Identifier: CA411100058

Gene: CHEK2

Linked Data

• MyVariant Identifiers: chr22:g.29095905A>T (hg19) ; chr22:g.28699917A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.28699917A>T , CM000684.2:g.28699917A>T	GRCh38
NC_000022.10:g.29095905A>T , CM000684.1:g.29095905A>T	GRCh37
NC_000022.9:g.27425905A>T	NCBI36
NG_008150.1:g.46918T>A
NG_008150.2:g.46950T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439346.6:c.838T>A	ENSP00000396903.2:n.838T>A
ENST00000711048.1:c.929T>A	ENSP00000518557.1:p.Phe310Tyr
ENST00000402731.6:c.728T>A	ENSP00000384835.2:p.Phe243Tyr
ENST00000404276.6:c.929T>A MANE Select	ENSP00000385747.1:p.Phe310Tyr
ENST00000425190.7:c.266T>A	ENSP00000390244.2:p.Phe89Tyr
ENST00000464581.6:c.269T>A	ENSP00000483777.2:p.Phe90Tyr
ENST00000648295.1:n.481T>A
ENST00000649563.1:c.266T>A	ENSP00000496928.1:p.Phe89Tyr
ENST00000650281.1:c.929T>A	ENSP00000497000.1:p.Phe310Tyr
ENST00000328354.10:c.929T>A	ENSP00000329178.6:p.Phe310Tyr
ENST00000348295.7:c.929T>A	ENSP00000329012.5:p.Phe310Tyr
ENST00000382580.6:c.1058T>A	ENSP00000372023.2:p.Phe353Tyr
ENST00000402731.5:c.929T>A	ENSP00000384835.1:p.Phe310Tyr
ENST00000403642.5:c.656T>A	ENSP00000384919.1:p.Phe219Tyr
ENST00000404276.5:c.929T>A	ENSP00000385747.1:p.Phe310Tyr
ENST00000405598.5:c.929T>A	ENSP00000386087.1:p.Phe310Tyr
ENST00000416671.5:c.*419T>A	ENSP00000402225.1:n.*419T>A
ENST00000417588.5:c.838T>A	ENSP00000412901.1:n.838T>A
ENST00000425190.6:c.266T>A	ENSP00000390244.1:p.Phe89Tyr
ENST00000433028.6:c.*654T>A	ENSP00000403659.1:n.*654T>A
ENST00000433728.5:c.867T>A	ENSP00000404400.1:p.Val289=
ENST00000434810.5:c.160T>A
ENST00000439346.5:c.400T>A	ENSP00000396903.1:n.400T>A
ENST00000447421.5:c.728T>A	ENSP00000397478.2:p.Phe243Tyr
ENST00000448511.5:c.819T>A	ENSP00000404567.1:n.819T>A
ENST00000456369.5:c.184T>A
ENST00000464581.5:c.269T>A	ENSP00000483777.1:p.Phe90Tyr
ENST00000491919.5:n.486T>A
NM_001005735.1:c.1058T>A	NP_001005735.1:p.Phe353Tyr
NM_001257387.1:c.266T>A	NP_001244316.1:p.Phe89Tyr
NM_007194.3:c.929T>A	NP_009125.1:p.Phe310Tyr
NM_145862.2:c.929T>A	NP_665861.1:p.Phe310Tyr
XM_006724114.2:c.449T>A	XP_006724177.1:p.Phe150Tyr
XM_006724116.2:c.386T>A	XP_006724179.2:p.Phe129Tyr
XM_011529839.1:c.1088T>A	XP_011528141.1:p.Phe363Tyr
XM_011529840.1:c.1088T>A	XP_011528142.1:p.Phe363Tyr
XM_011529841.1:c.857T>A	XP_011528143.1:p.Phe286Tyr
XM_011529842.1:c.758T>A	XP_011528144.1:p.Phe253Tyr
XM_011529843.1:c.728T>A	XP_011528145.1:p.Phe243Tyr
XM_011529844.1:c.1088T>A	XP_011528146.1:p.Phe363Tyr
XM_011529845.1:c.266T>A	XP_011528147.1:p.Phe89Tyr
XR_937805.1:n.1088T>A
XR_937806.1:n.1083T>A
XR_937807.1:n.1083T>A
NM_001349956.1:c.728T>A	NP_001336885.1:p.Phe243Tyr
NM_007194.4:c.929T>A MANE Select	NP_009125.1:p.Phe310Tyr
XM_006724114.3:c.482T>A	XP_006724177.2:p.Phe161Tyr
XM_011529839.2:c.1088T>A	XP_011528141.1:p.Phe363Tyr
XM_011529840.3:c.1088T>A	XP_011528142.1:p.Phe363Tyr
XM_011529842.2:c.758T>A	XP_011528144.1:p.Phe253Tyr
XM_011529844.2:c.1088T>A	XP_011528146.1:p.Phe363Tyr
XM_011529845.2:c.266T>A	XP_011528147.1:p.Phe89Tyr
XM_017028560.1:c.1052T>A	XP_016884049.1:p.Phe351Tyr
XM_017028561.2:c.266T>A	XP_016884050.1:p.Phe89Tyr
XM_024452148.1:c.959T>A	XP_024307916.1:p.Phe320Tyr
XM_024452149.1:c.959T>A	XP_024307917.1:p.Phe320Tyr
XR_937805.2:n.1099T>A
XR_937806.2:n.1099T>A
XR_937807.2:n.1099T>A
NM_001005735.2:c.1058T>A	NP_001005735.1:p.Phe353Tyr
NM_001257387.2:c.266T>A	NP_001244316.1:p.Phe89Tyr
NM_001349956.2:c.728T>A	NP_001336885.1:p.Phe243Tyr