Canonical Allele Identifier: CA2400237508
Gene: CHEK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.28694081G= , CM000684.2:g.28694081G= GRCh38
NC_000022.10:g.29090069G= , CM000684.1:g.29090069G= GRCh37
NC_000022.9:g.27420069G= NCBI36
NG_008150.1:g.52754C=
NG_008150.2:g.52786C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000711048.1:c.*147C= ENSP00000518557.1:n.*147C=
ENST00000402731.6:c.1211C= ENSP00000384835.2:p.Pro404=
ENST00000404276.6:c.1412C= MANE Select ENSP00000385747.1:p.Pro471=
ENST00000425190.7:c.749C= ENSP00000390244.2:p.Pro250=
ENST00000464581.6:c.752C= ENSP00000483777.2:p.Pro251=
ENST00000648295.1:n.964C=
ENST00000649563.1:c.749C= ENSP00000496928.1:p.Pro250=
ENST00000650281.1:c.1412C= ENSP00000497000.1:p.Pro471=
ENST00000328354.10:c.1412C= ENSP00000329178.6:p.Pro471=
ENST00000348295.7:c.1325C= ENSP00000329012.5:p.Pro442=
ENST00000382580.6:c.1541C= ENSP00000372023.2:p.Pro514=
ENST00000402731.5:c.1325C= ENSP00000384835.1:p.Pro442=
ENST00000403642.5:c.1139C= ENSP00000384919.1:p.Pro380=
ENST00000404276.5:c.1412C= ENSP00000385747.1:p.Pro471=
ENST00000405598.5:c.1412C= ENSP00000386087.1:p.Pro471=
ENST00000416671.5:c.*902C= ENSP00000402225.1:n.*902C=
ENST00000417588.5:c.1321C= ENSP00000412901.1:n.1321C=
ENST00000433728.5:c.1350C= ENSP00000404400.1:n.1350C=
ENST00000434810.5:c.610C=
ENST00000448511.5:c.1302C= ENSP00000404567.1:n.1302C=
ENST00000456369.5:c.264-4866C=
NM_001005735.1:c.1541C= NP_001005735.1:p.Pro514=
NM_001257387.1:c.749C= NP_001244316.1:p.Pro250=
NM_007194.3:c.1412C= NP_009125.1:p.Pro471=
NM_145862.2:c.1325C= NP_665861.1:p.Pro442=
XM_006724114.2:c.932C= XP_006724177.1:p.Pro311=
XM_006724116.2:c.869C= XP_006724179.2:p.Pro290=
XM_011529839.1:c.1571C= XP_011528141.1:p.Pro524=
XM_011529840.1:c.1484C= XP_011528142.1:p.Pro495=
XM_011529841.1:c.1340C= XP_011528143.1:p.Pro447=
XM_011529842.1:c.1241C= XP_011528144.1:p.Pro414=
XM_011529843.1:c.1211C= XP_011528145.1:p.Pro404=
XM_011529845.1:c.749C= XP_011528147.1:p.Pro250=
XR_937805.1:n.1571C=
NM_001349956.1:c.1211C= NP_001336885.1:p.Pro404=
NM_007194.4:c.1412C= MANE Select NP_009125.1:p.Pro471=
XM_006724114.3:c.965C= XP_006724177.2:p.Pro322=
XM_011529839.2:c.1571C= XP_011528141.1:p.Pro524=
XM_011529840.3:c.1484C= XP_011528142.1:p.Pro495=
XM_011529842.2:c.1241C= XP_011528144.1:p.Pro414=
XM_011529845.2:c.749C= XP_011528147.1:p.Pro250=
XM_017028560.1:c.1535C= XP_016884049.1:p.Pro512=
XM_017028561.2:c.749C= XP_016884050.1:p.Pro250=
XM_024452148.1:c.1442C= XP_024307916.1:p.Pro481=
XM_024452149.1:c.1355C= XP_024307917.1:p.Pro452=
XR_937805.2:n.1582C=
NM_001005735.2:c.1541C= NP_001005735.1:p.Pro514=
NM_001257387.2:c.749C= NP_001244316.1:p.Pro250=
NM_001349956.2:c.1211C= NP_001336885.1:p.Pro404=