Canonical Allele Identifier: CA2400238850
Gene: CHEK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.28696950T= , CM000684.2:g.28696950T= GRCh38
NC_000022.10:g.29092938T= , CM000684.1:g.29092938T= GRCh37
NC_000022.9:g.27422938T= NCBI36
NG_008150.1:g.49885A=
NG_008150.2:g.49917A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000711048.1:c.1009-1708A= ENSP00000518557.1:n.1009-1708A=
ENST00000402731.6:c.845A= ENSP00000384835.2:p.Lys282=
ENST00000404276.6:c.1046A= MANE Select ENSP00000385747.1:p.Lys349=
ENST00000425190.7:c.383A= ENSP00000390244.2:p.Lys128=
ENST00000464581.6:c.386A= ENSP00000483777.2:p.Lys129=
ENST00000648295.1:n.598A=
ENST00000649563.1:c.383A= ENSP00000496928.1:p.Lys128=
ENST00000650281.1:c.1046A= ENSP00000497000.1:p.Lys349=
ENST00000328354.10:c.1046A= ENSP00000329178.6:p.Lys349=
ENST00000348295.7:c.1009-1077A= ENSP00000329012.5:n.1009-1077A=
ENST00000382580.6:c.1175A= ENSP00000372023.2:p.Lys392=
ENST00000402731.5:c.1009-1077A= ENSP00000384835.1:n.1009-1077A=
ENST00000403642.5:c.773A= ENSP00000384919.1:p.Lys258=
ENST00000404276.5:c.1046A= ENSP00000385747.1:p.Lys349=
ENST00000405598.5:c.1046A= ENSP00000386087.1:p.Lys349=
ENST00000416671.5:c.*536A= ENSP00000402225.1:n.*536A=
ENST00000417588.5:c.955A= ENSP00000412901.1:n.955A=
ENST00000433028.6:c.*771A= ENSP00000403659.1:n.*771A=
ENST00000433728.5:c.984A= ENSP00000404400.1:n.984A=
ENST00000434810.5:c.277A=
ENST00000447421.5:c.845A= ENSP00000397478.2:p.Lys282=
ENST00000448511.5:c.936A= ENSP00000404567.1:n.936A=
ENST00000456369.5:c.263+2888A=
ENST00000464581.5:c.386A= ENSP00000483777.1:p.Lys129=
ENST00000491919.5:n.603A=
NM_001005735.1:c.1175A= NP_001005735.1:p.Lys392=
NM_001257387.1:c.383A= NP_001244316.1:p.Lys128=
NM_007194.3:c.1046A= NP_009125.1:p.Lys349=
NM_145862.2:c.1009-1077A= NP_665861.1:n.1009-1077A=
XM_006724114.2:c.566A= XP_006724177.1:p.Lys189=
XM_006724116.2:c.503A= XP_006724179.2:p.Lys168=
XM_011529839.1:c.1205A= XP_011528141.1:p.Lys402=
XM_011529840.1:c.1168-1077A= XP_011528142.1:n.1168-1077A=
XM_011529841.1:c.974A= XP_011528143.1:p.Lys325=
XM_011529842.1:c.875A= XP_011528144.1:p.Lys292=
XM_011529843.1:c.845A= XP_011528145.1:p.Lys282=
XM_011529845.1:c.383A= XP_011528147.1:p.Lys128=
XR_937805.1:n.1205A=
XR_937806.1:n.1163-1077A=
NM_001349956.1:c.845A= NP_001336885.1:p.Lys282=
NM_007194.4:c.1046A= MANE Select NP_009125.1:p.Lys349=
XM_006724114.3:c.599A= XP_006724177.2:p.Lys200=
XM_011529839.2:c.1205A= XP_011528141.1:p.Lys402=
XM_011529840.3:c.1168-1077A= XP_011528142.1:n.1168-1077A=
XM_011529842.2:c.875A= XP_011528144.1:p.Lys292=
XM_011529845.2:c.383A= XP_011528147.1:p.Lys128=
XM_017028560.1:c.1169A= XP_016884049.1:p.Lys390=
XM_017028561.2:c.383A= XP_016884050.1:p.Lys128=
XM_024452148.1:c.1076A= XP_024307916.1:p.Lys359=
XM_024452149.1:c.1039-1077A= XP_024307917.1:n.1039-1077A=
XR_937805.2:n.1216A=
XR_937806.2:n.1179-1077A=
NM_001005735.2:c.1175A= NP_001005735.1:p.Lys392=
NM_001257387.2:c.383A= NP_001244316.1:p.Lys128=
NM_001349956.2:c.845A= NP_001336885.1:p.Lys282=