Canonical Allele Identifier: CA2400237513
Gene: CHEK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.28694085C= , CM000684.2:g.28694085C= GRCh38
NC_000022.10:g.29090073C= , CM000684.1:g.29090073C= GRCh37
NC_000022.9:g.27420073C= NCBI36
NG_008150.1:g.52750G=
NG_008150.2:g.52782G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000711048.1:c.*143G= ENSP00000518557.1:n.*143G=
ENST00000402731.6:c.1207G= ENSP00000384835.2:p.Asp403=
ENST00000404276.6:c.1408G= MANE Select ENSP00000385747.1:p.Asp470=
ENST00000425190.7:c.745G= ENSP00000390244.2:p.Asp249=
ENST00000464581.6:c.748G= ENSP00000483777.2:p.Asp250=
ENST00000648295.1:n.960G=
ENST00000649563.1:c.745G= ENSP00000496928.1:p.Asp249=
ENST00000650281.1:c.1408G= ENSP00000497000.1:p.Asp470=
ENST00000328354.10:c.1408G= ENSP00000329178.6:p.Asp470=
ENST00000348295.7:c.1321G= ENSP00000329012.5:p.Asp441=
ENST00000382580.6:c.1537G= ENSP00000372023.2:p.Asp513=
ENST00000402731.5:c.1321G= ENSP00000384835.1:p.Asp441=
ENST00000403642.5:c.1135G= ENSP00000384919.1:p.Asp379=
ENST00000404276.5:c.1408G= ENSP00000385747.1:p.Asp470=
ENST00000405598.5:c.1408G= ENSP00000386087.1:p.Asp470=
ENST00000416671.5:c.*898G= ENSP00000402225.1:n.*898G=
ENST00000417588.5:c.1317G= ENSP00000412901.1:n.1317G=
ENST00000433728.5:c.1346G= ENSP00000404400.1:n.1346G=
ENST00000434810.5:c.606G=
ENST00000448511.5:c.1298G= ENSP00000404567.1:n.1298G=
ENST00000456369.5:c.264-4870G=
NM_001005735.1:c.1537G= NP_001005735.1:p.Asp513=
NM_001257387.1:c.745G= NP_001244316.1:p.Asp249=
NM_007194.3:c.1408G= NP_009125.1:p.Asp470=
NM_145862.2:c.1321G= NP_665861.1:p.Asp441=
XM_006724114.2:c.928G= XP_006724177.1:p.Asp310=
XM_006724116.2:c.865G= XP_006724179.2:p.Asp289=
XM_011529839.1:c.1567G= XP_011528141.1:p.Asp523=
XM_011529840.1:c.1480G= XP_011528142.1:p.Asp494=
XM_011529841.1:c.1336G= XP_011528143.1:p.Asp446=
XM_011529842.1:c.1237G= XP_011528144.1:p.Asp413=
XM_011529843.1:c.1207G= XP_011528145.1:p.Asp403=
XM_011529845.1:c.745G= XP_011528147.1:p.Asp249=
XR_937805.1:n.1567G=
NM_001349956.1:c.1207G= NP_001336885.1:p.Asp403=
NM_007194.4:c.1408G= MANE Select NP_009125.1:p.Asp470=
XM_006724114.3:c.961G= XP_006724177.2:p.Asp321=
XM_011529839.2:c.1567G= XP_011528141.1:p.Asp523=
XM_011529840.3:c.1480G= XP_011528142.1:p.Asp494=
XM_011529842.2:c.1237G= XP_011528144.1:p.Asp413=
XM_011529845.2:c.745G= XP_011528147.1:p.Asp249=
XM_017028560.1:c.1531G= XP_016884049.1:p.Asp511=
XM_017028561.2:c.745G= XP_016884050.1:p.Asp249=
XM_024452148.1:c.1438G= XP_024307916.1:p.Asp480=
XM_024452149.1:c.1351G= XP_024307917.1:p.Asp451=
XR_937805.2:n.1578G=
NM_001005735.2:c.1537G= NP_001005735.1:p.Asp513=
NM_001257387.2:c.745G= NP_001244316.1:p.Asp249=
NM_001349956.2:c.1207G= NP_001336885.1:p.Asp403=