Canonical Allele Identifier: CA2400238878
Gene: CHEK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.28696984G= , CM000684.2:g.28696984G= GRCh38
NC_000022.10:g.29092972G= , CM000684.1:g.29092972G= GRCh37
NC_000022.9:g.27422972G= NCBI36
NG_008150.1:g.49851C=
NG_008150.2:g.49883C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000711048.1:c.1009-1742C= ENSP00000518557.1:n.1009-1742C=
ENST00000402731.6:c.811C= ENSP00000384835.2:p.Leu271=
ENST00000404276.6:c.1012C= MANE Select ENSP00000385747.1:p.Leu338=
ENST00000425190.7:c.349C= ENSP00000390244.2:p.Leu117=
ENST00000464581.6:c.352C= ENSP00000483777.2:p.Leu118=
ENST00000648295.1:n.564C=
ENST00000649563.1:c.349C= ENSP00000496928.1:p.Leu117=
ENST00000650281.1:c.1012C= ENSP00000497000.1:p.Leu338=
ENST00000328354.10:c.1012C= ENSP00000329178.6:p.Leu338=
ENST00000348295.7:c.1009-1111C= ENSP00000329012.5:n.1009-1111C=
ENST00000382580.6:c.1141C= ENSP00000372023.2:p.Leu381=
ENST00000402731.5:c.1009-1111C= ENSP00000384835.1:n.1009-1111C=
ENST00000403642.5:c.739C= ENSP00000384919.1:p.Leu247=
ENST00000404276.5:c.1012C= ENSP00000385747.1:p.Leu338=
ENST00000405598.5:c.1012C= ENSP00000386087.1:p.Leu338=
ENST00000416671.5:c.*502C= ENSP00000402225.1:n.*502C=
ENST00000417588.5:c.921C= ENSP00000412901.1:n.921C=
ENST00000425190.6:c.349C= ENSP00000390244.1:p.Leu117=
ENST00000433028.6:c.*737C= ENSP00000403659.1:n.*737C=
ENST00000433728.5:c.950C= ENSP00000404400.1:n.950C=
ENST00000434810.5:c.243C=
ENST00000447421.5:c.811C= ENSP00000397478.2:p.Leu271=
ENST00000448511.5:c.902C= ENSP00000404567.1:n.902C=
ENST00000456369.5:c.263+2854C=
ENST00000464581.5:c.352C= ENSP00000483777.1:p.Leu118=
ENST00000491919.5:n.569C=
NM_001005735.1:c.1141C= NP_001005735.1:p.Leu381=
NM_001257387.1:c.349C= NP_001244316.1:p.Leu117=
NM_007194.3:c.1012C= NP_009125.1:p.Leu338=
NM_145862.2:c.1009-1111C= NP_665861.1:n.1009-1111C=
XM_006724114.2:c.532C= XP_006724177.1:p.Leu178=
XM_006724116.2:c.469C= XP_006724179.2:p.Leu157=
XM_011529839.1:c.1171C= XP_011528141.1:p.Leu391=
XM_011529840.1:c.1168-1111C= XP_011528142.1:n.1168-1111C=
XM_011529841.1:c.940C= XP_011528143.1:p.Leu314=
XM_011529842.1:c.841C= XP_011528144.1:p.Leu281=
XM_011529843.1:c.811C= XP_011528145.1:p.Leu271=
XM_011529845.1:c.349C= XP_011528147.1:p.Leu117=
XR_937805.1:n.1171C=
XR_937806.1:n.1163-1111C=
NM_001349956.1:c.811C= NP_001336885.1:p.Leu271=
NM_007194.4:c.1012C= MANE Select NP_009125.1:p.Leu338=
XM_006724114.3:c.565C= XP_006724177.2:p.Leu189=
XM_011529839.2:c.1171C= XP_011528141.1:p.Leu391=
XM_011529840.3:c.1168-1111C= XP_011528142.1:n.1168-1111C=
XM_011529842.2:c.841C= XP_011528144.1:p.Leu281=
XM_011529845.2:c.349C= XP_011528147.1:p.Leu117=
XM_017028560.1:c.1135C= XP_016884049.1:p.Leu379=
XM_017028561.2:c.349C= XP_016884050.1:p.Leu117=
XM_024452148.1:c.1042C= XP_024307916.1:p.Leu348=
XM_024452149.1:c.1039-1111C= XP_024307917.1:n.1039-1111C=
XR_937805.2:n.1182C=
XR_937806.2:n.1179-1111C=
NM_001005735.2:c.1141C= NP_001005735.1:p.Leu381=
NM_001257387.2:c.349C= NP_001244316.1:p.Leu117=
NM_001349956.2:c.811C= NP_001336885.1:p.Leu271=