Canonical Allele Identifier: CA2640620627
Gene: CSNK1D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82265778_82265780del , CM000679.2:g.82265778_82265780del GRCh38
NC_000017.10:g.80223654_80223656del , CM000679.1:g.80223654_80223656del GRCh37
NC_000017.9:g.77816943_77816945del NCBI36
NG_012828.1:g.12920_12922del
NG_012828.2:g.12965_12967del

Transcript Alleles

HGVS Amino-acid Change
ENST00000392334.7:c.95_97del ENSP00000376146.2:p.Gly32del
ENST00000314028.11:c.95_97del MANE Select ENSP00000324464.6:p.Gly32del
ENST00000314028.10:c.95_97del ENSP00000324464.6:p.Gly32del
ENST00000392334.6:c.95_97del ENSP00000376146.2:p.Gly32del
ENST00000398519.9:c.95_97del ENSP00000381531.5:p.Gly32del
ENST00000403276.7:c.95_97del ENSP00000385769.3:p.Gly32del
ENST00000578194.5:n.301_303del
ENST00000579308.1:n.120_122del
ENST00000579316.5:n.152_154del
ENST00000580061.5:n.95_97del
ENST00000580446.1:c.76+7528_76+7530del ENSP00000463757.1:n.76+7528_76+7530del
ENST00000581241.5:n.83_85del
ENST00000581660.5:c.*133_*135del ENSP00000464551.1:n.*133_*135del
ENST00000582844.5:n.53_55del
ENST00000584472.5:n.180_182del
ENST00000585026.1:c.*141_*143del ENSP00000462144.1:n.*141_*143del
NM_001893.4:c.95_97del NP_001884.2:p.Gly32del
NM_139062.2:c.95_97del NP_620693.1:p.Gly32del
NR_110578.1:n.456_458del
XM_005256336.2:c.95_97del XP_005256393.1:p.Gly32del
XM_005256337.3:c.95_97del XP_005256394.1:p.Gly32del
XR_243518.2:n.415_417del
XR_430028.2:n.415_417del
XR_933922.1:n.415_417del
XR_933923.1:n.415_417del
NM_001363749.1:c.95_97del NP_001350678.1:p.Gly32del
NM_001893.5:c.95_97del NP_001884.2:p.Gly32del
NM_139062.3:c.95_97del NP_620693.1:p.Gly32del
NR_110578.2:n.464_466del
XM_005256336.4:c.95_97del XP_005256393.1:p.Gly32del
XR_002957961.1:n.414_416del
XR_243518.4:n.414_416del
XR_430028.4:n.414_416del
XR_933922.3:n.414_416del
XR_933923.3:n.414_416del
NM_001363749.2:c.95_97del NP_001350678.1:p.Gly32del
NM_001893.6:c.95_97del MANE Select NP_001884.2:p.Gly32del
NM_139062.4:c.95_97del NP_620693.1:p.Gly32del