Canonical Allele Identifier: CA2400238848
Gene: CHEK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.28696946T= , CM000684.2:g.28696946T= GRCh38
NC_000022.10:g.29092934T= , CM000684.1:g.29092934T= GRCh37
NC_000022.9:g.27422934T= NCBI36
NG_008150.1:g.49889A=
NG_008150.2:g.49921A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000711048.1:c.1009-1704A= ENSP00000518557.1:n.1009-1704A=
ENST00000402731.6:c.849A= ENSP00000384835.2:p.Pro283=
ENST00000404276.6:c.1050A= MANE Select ENSP00000385747.1:p.Pro350=
ENST00000425190.7:c.387A= ENSP00000390244.2:p.Pro129=
ENST00000464581.6:c.390A= ENSP00000483777.2:p.Pro130=
ENST00000648295.1:n.602A=
ENST00000649563.1:c.387A= ENSP00000496928.1:p.Pro129=
ENST00000650281.1:c.1050A= ENSP00000497000.1:p.Pro350=
ENST00000328354.10:c.1050A= ENSP00000329178.6:p.Pro350=
ENST00000348295.7:c.1009-1073A= ENSP00000329012.5:n.1009-1073A=
ENST00000382580.6:c.1179A= ENSP00000372023.2:p.Pro393=
ENST00000402731.5:c.1009-1073A= ENSP00000384835.1:n.1009-1073A=
ENST00000403642.5:c.777A= ENSP00000384919.1:p.Pro259=
ENST00000404276.5:c.1050A= ENSP00000385747.1:p.Pro350=
ENST00000405598.5:c.1050A= ENSP00000386087.1:p.Pro350=
ENST00000416671.5:c.*540A= ENSP00000402225.1:n.*540A=
ENST00000417588.5:c.959A= ENSP00000412901.1:n.959A=
ENST00000433028.6:c.*775A= ENSP00000403659.1:n.*775A=
ENST00000433728.5:c.988A= ENSP00000404400.1:n.988A=
ENST00000434810.5:c.281A=
ENST00000447421.5:c.849A= ENSP00000397478.2:p.Pro283=
ENST00000448511.5:c.940A= ENSP00000404567.1:n.940A=
ENST00000456369.5:c.263+2892A=
ENST00000464581.5:c.390A= ENSP00000483777.1:p.Pro130=
ENST00000491919.5:n.607A=
NM_001005735.1:c.1179A= NP_001005735.1:p.Pro393=
NM_001257387.1:c.387A= NP_001244316.1:p.Pro129=
NM_007194.3:c.1050A= NP_009125.1:p.Pro350=
NM_145862.2:c.1009-1073A= NP_665861.1:n.1009-1073A=
XM_006724114.2:c.570A= XP_006724177.1:p.Pro190=
XM_006724116.2:c.507A= XP_006724179.2:p.Pro169=
XM_011529839.1:c.1209A= XP_011528141.1:p.Pro403=
XM_011529840.1:c.1168-1073A= XP_011528142.1:n.1168-1073A=
XM_011529841.1:c.978A= XP_011528143.1:p.Pro326=
XM_011529842.1:c.879A= XP_011528144.1:p.Pro293=
XM_011529843.1:c.849A= XP_011528145.1:p.Pro283=
XM_011529845.1:c.387A= XP_011528147.1:p.Pro129=
XR_937805.1:n.1209A=
XR_937806.1:n.1163-1073A=
NM_001349956.1:c.849A= NP_001336885.1:p.Pro283=
NM_007194.4:c.1050A= MANE Select NP_009125.1:p.Pro350=
XM_006724114.3:c.603A= XP_006724177.2:p.Pro201=
XM_011529839.2:c.1209A= XP_011528141.1:p.Pro403=
XM_011529840.3:c.1168-1073A= XP_011528142.1:n.1168-1073A=
XM_011529842.2:c.879A= XP_011528144.1:p.Pro293=
XM_011529845.2:c.387A= XP_011528147.1:p.Pro129=
XM_017028560.1:c.1173A= XP_016884049.1:p.Pro391=
XM_017028561.2:c.387A= XP_016884050.1:p.Pro129=
XM_024452148.1:c.1080A= XP_024307916.1:p.Pro360=
XM_024452149.1:c.1039-1073A= XP_024307917.1:n.1039-1073A=
XR_937805.2:n.1220A=
XR_937806.2:n.1179-1073A=
NM_001005735.2:c.1179A= NP_001005735.1:p.Pro393=
NM_001257387.2:c.387A= NP_001244316.1:p.Pro129=
NM_001349956.2:c.849A= NP_001336885.1:p.Pro283=