Canonical Allele Identifier: CA2400238833
Gene: CHEK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.28696931C= , CM000684.2:g.28696931C= GRCh38
NC_000022.10:g.29092919C= , CM000684.1:g.29092919C= GRCh37
NC_000022.9:g.27422919C= NCBI36
NG_008150.1:g.49904G=
NG_008150.2:g.49936G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000711048.1:c.1009-1689G= ENSP00000518557.1:n.1009-1689G=
ENST00000402731.6:c.864G= ENSP00000384835.2:p.Leu288=
ENST00000404276.6:c.1065G= MANE Select ENSP00000385747.1:p.Leu355=
ENST00000425190.7:c.402G= ENSP00000390244.2:p.Leu134=
ENST00000464581.6:c.405G= ENSP00000483777.2:p.Leu135=
ENST00000648295.1:n.617G=
ENST00000649563.1:c.402G= ENSP00000496928.1:p.Leu134=
ENST00000650281.1:c.1065G= ENSP00000497000.1:p.Leu355=
ENST00000328354.10:c.1065G= ENSP00000329178.6:p.Leu355=
ENST00000348295.7:c.1009-1058G= ENSP00000329012.5:n.1009-1058G=
ENST00000382580.6:c.1194G= ENSP00000372023.2:p.Leu398=
ENST00000402731.5:c.1009-1058G= ENSP00000384835.1:n.1009-1058G=
ENST00000403642.5:c.792G= ENSP00000384919.1:p.Leu264=
ENST00000404276.5:c.1065G= ENSP00000385747.1:p.Leu355=
ENST00000405598.5:c.1065G= ENSP00000386087.1:p.Leu355=
ENST00000416671.5:c.*555G= ENSP00000402225.1:n.*555G=
ENST00000417588.5:c.974G= ENSP00000412901.1:n.974G=
ENST00000433028.6:c.*790G= ENSP00000403659.1:n.*790G=
ENST00000433728.5:c.1003G= ENSP00000404400.1:n.1003G=
ENST00000434810.5:c.296G=
ENST00000447421.5:c.864G= ENSP00000397478.2:p.Leu288=
ENST00000448511.5:c.955G= ENSP00000404567.1:n.955G=
ENST00000456369.5:c.263+2907G=
ENST00000464581.5:c.405G= ENSP00000483777.1:p.Leu135=
NM_001005735.1:c.1194G= NP_001005735.1:p.Leu398=
NM_001257387.1:c.402G= NP_001244316.1:p.Leu134=
NM_007194.3:c.1065G= NP_009125.1:p.Leu355=
NM_145862.2:c.1009-1058G= NP_665861.1:n.1009-1058G=
XM_006724114.2:c.585G= XP_006724177.1:p.Leu195=
XM_006724116.2:c.522G= XP_006724179.2:p.Leu174=
XM_011529839.1:c.1224G= XP_011528141.1:p.Leu408=
XM_011529840.1:c.1168-1058G= XP_011528142.1:n.1168-1058G=
XM_011529841.1:c.993G= XP_011528143.1:p.Leu331=
XM_011529842.1:c.894G= XP_011528144.1:p.Leu298=
XM_011529843.1:c.864G= XP_011528145.1:p.Leu288=
XM_011529845.1:c.402G= XP_011528147.1:p.Leu134=
XR_937805.1:n.1224G=
XR_937806.1:n.1163-1058G=
NM_001349956.1:c.864G= NP_001336885.1:p.Leu288=
NM_007194.4:c.1065G= MANE Select NP_009125.1:p.Leu355=
XM_006724114.3:c.618G= XP_006724177.2:p.Leu206=
XM_011529839.2:c.1224G= XP_011528141.1:p.Leu408=
XM_011529840.3:c.1168-1058G= XP_011528142.1:n.1168-1058G=
XM_011529842.2:c.894G= XP_011528144.1:p.Leu298=
XM_011529845.2:c.402G= XP_011528147.1:p.Leu134=
XM_017028560.1:c.1188G= XP_016884049.1:p.Leu396=
XM_017028561.2:c.402G= XP_016884050.1:p.Leu134=
XM_024452148.1:c.1095G= XP_024307916.1:p.Leu365=
XM_024452149.1:c.1039-1058G= XP_024307917.1:n.1039-1058G=
XR_937805.2:n.1235G=
XR_937806.2:n.1179-1058G=
NM_001005735.2:c.1194G= NP_001005735.1:p.Leu398=
NM_001257387.2:c.402G= NP_001244316.1:p.Leu134=
NM_001349956.2:c.864G= NP_001336885.1:p.Leu288=