Canonical Allele Identifier: CA2400240182
Gene: CHEK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.28699855T= , CM000684.2:g.28699855T= GRCh38
NC_000022.10:g.29095843T= , CM000684.1:g.29095843T= GRCh37
NC_000022.9:g.27425843T= NCBI36
NG_008150.1:g.46980A=
NG_008150.2:g.47012A=

Transcript Alleles

HGVS Amino-acid change
ENST00000439346.6:c.900A= ENSP00000396903.2:n.900A=
ENST00000711048.1:c.991A= ENSP00000518557.1:p.Met331=
ENST00000402731.6:c.790A= ENSP00000384835.2:p.Met264=
ENST00000404276.6:c.991A= MANE Select ENSP00000385747.1:p.Met331=
ENST00000425190.7:c.328A= ENSP00000390244.2:p.Met110=
ENST00000464581.6:c.331A= ENSP00000483777.2:p.Met111=
ENST00000648295.1:n.543A=
ENST00000649563.1:c.328A= ENSP00000496928.1:p.Met110=
ENST00000650281.1:c.991A= ENSP00000497000.1:p.Met331=
ENST00000328354.10:c.991A= ENSP00000329178.6:p.Met331=
ENST00000348295.7:c.991A= ENSP00000329012.5:p.Met331=
ENST00000382580.6:c.1120A= ENSP00000372023.2:p.Met374=
ENST00000402731.5:c.991A= ENSP00000384835.1:p.Met331=
ENST00000403642.5:c.718A= ENSP00000384919.1:p.Met240=
ENST00000404276.5:c.991A= ENSP00000385747.1:p.Met331=
ENST00000405598.5:c.991A= ENSP00000386087.1:p.Met331=
ENST00000416671.5:c.*481A= ENSP00000402225.1:n.*481A=
ENST00000417588.5:c.900A= ENSP00000412901.1:n.900A=
ENST00000425190.6:c.328A= ENSP00000390244.1:p.Met110=
ENST00000433028.6:c.*716A= ENSP00000403659.1:n.*716A=
ENST00000433728.5:c.929A= ENSP00000404400.1:n.929A=
ENST00000434810.5:c.222A=
ENST00000439346.5:c.462A= ENSP00000396903.1:n.462A=
ENST00000447421.5:c.790A= ENSP00000397478.2:p.Met264=
ENST00000448511.5:c.881A= ENSP00000404567.1:n.881A=
ENST00000456369.5:c.246A=
ENST00000464581.5:c.331A= ENSP00000483777.1:p.Met111=
ENST00000491919.5:n.548A=
NM_001005735.1:c.1120A= NP_001005735.1:p.Met374=
NM_001257387.1:c.328A= NP_001244316.1:p.Met110=
NM_007194.3:c.991A= NP_009125.1:p.Met331=
NM_145862.2:c.991A= NP_665861.1:p.Met331=
XM_006724114.2:c.511A= XP_006724177.1:p.Met171=
XM_006724116.2:c.448A= XP_006724179.2:p.Met150=
XM_011529839.1:c.1150A= XP_011528141.1:p.Met384=
XM_011529840.1:c.1150A= XP_011528142.1:p.Met384=
XM_011529841.1:c.919A= XP_011528143.1:p.Met307=
XM_011529842.1:c.820A= XP_011528144.1:p.Met274=
XM_011529843.1:c.790A= XP_011528145.1:p.Met264=
XM_011529844.1:c.1150A= XP_011528146.1:p.Met384=
XM_011529845.1:c.328A= XP_011528147.1:p.Met110=
XR_937805.1:n.1150A=
XR_937806.1:n.1145A=
XR_937807.1:n.1145A=
NM_001349956.1:c.790A= NP_001336885.1:p.Met264=
NM_007194.4:c.991A= MANE Select NP_009125.1:p.Met331=
XM_006724114.3:c.544A= XP_006724177.2:p.Met182=
XM_011529839.2:c.1150A= XP_011528141.1:p.Met384=
XM_011529840.3:c.1150A= XP_011528142.1:p.Met384=
XM_011529842.2:c.820A= XP_011528144.1:p.Met274=
XM_011529844.2:c.1150A= XP_011528146.1:p.Met384=
XM_011529845.2:c.328A= XP_011528147.1:p.Met110=
XM_017028560.1:c.1114A= XP_016884049.1:p.Met372=
XM_017028561.2:c.328A= XP_016884050.1:p.Met110=
XM_024452148.1:c.1021A= XP_024307916.1:p.Met341=
XM_024452149.1:c.1021A= XP_024307917.1:p.Met341=
XR_937805.2:n.1161A=
XR_937806.2:n.1161A=
XR_937807.2:n.1161A=
NM_001005735.2:c.1120A= NP_001005735.1:p.Met374=
NM_001257387.2:c.328A= NP_001244316.1:p.Met110=
NM_001349956.2:c.790A= NP_001336885.1:p.Met264=