Canonical Allele Identifier: CA2278929906

Gene: CSNK1D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265462_82265470delinsAGCCACCAT , CM000679.2:g.82265462_82265470delinsAGCCACCAT	GRCh38
NC_000017.10:g.80223338_80223346delinsAGCCACCAT , CM000679.1:g.80223338_80223346delinsAGCCACCAT	GRCh37
NC_000017.9:g.77816627_77816635delinsAGCCACCAT	NCBI36
NG_012828.1:g.13228_13236delinsATGGTGGCT
NG_012828.2:g.13273_13281delinsATGGTGGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.187+216_187+224delinsATGGTGGCT	ENSP00000376146.2:n.187+216_187+224delinsATGGTGGCT
ENST00000314028.11:c.187+216_187+224delinsATGGTGGCT MANE Select	ENSP00000324464.6:n.187+216_187+224delinsATGGTGGCT
ENST00000314028.10:c.187+216_187+224delinsATGGTGGCT	ENSP00000324464.6:n.187+216_187+224delinsATGGTGGCT
ENST00000392334.6:c.187+216_187+224delinsATGGTGGCT	ENSP00000376146.2:n.187+216_187+224delinsATGGTGGCT
ENST00000398519.9:c.187+216_187+224delinsATGGTGGCT	ENSP00000381531.5:n.187+216_187+224delinsATGGTGGCT
ENST00000403276.7:c.187+216_187+224delinsATGGTGGCT	ENSP00000385769.3:n.187+216_187+224delinsATGGTGGCT
ENST00000578194.5:n.393+216_393+224delinsATGGTGGCT
ENST00000579308.1:n.428_436delinsATGGTGGCT
ENST00000579316.5:n.244+216_244+224delinsATGGTGGCT
ENST00000580061.5:n.187+216_187+224delinsATGGTGGCT
ENST00000580446.1:c.76+7836_76+7844delinsATGGTGGCT	ENSP00000463757.1:n.76+7836_76+7844delinsATGGTGGCT
ENST00000581241.5:n.175+216_175+224delinsATGGTGGCT
ENST00000581660.5:c.*225+216_*225+224delinsATGGTGGCT	ENSP00000464551.1:n.*225+216_*225+224delinsATGGTGGCT
ENST00000582844.5:n.145+216_145+224delinsATGGTGGCT
ENST00000584472.5:n.272+216_272+224delinsATGGTGGCT
ENST00000585026.1:c.*233+216_*233+224delinsATGGTGGCT	ENSP00000462144.1:n.*233+216_*233+224delinsATGGTGGCT
NM_001893.4:c.187+216_187+224delinsATGGTGGCT	NP_001884.2:n.187+216_187+224delinsATGGTGGCT
NM_139062.2:c.187+216_187+224delinsATGGTGGCT	NP_620693.1:n.187+216_187+224delinsATGGTGGCT
NR_110578.1:n.548+216_548+224delinsATGGTGGCT
XM_005256336.2:c.187+216_187+224delinsATGGTGGCT	XP_005256393.1:n.187+216_187+224delinsATGGTGGCT
XM_005256337.3:c.187+216_187+224delinsATGGTGGCT	XP_005256394.1:n.187+216_187+224delinsATGGTGGCT
XR_243518.2:n.507+216_507+224delinsATGGTGGCT
XR_430028.2:n.507+216_507+224delinsATGGTGGCT
XR_933922.1:n.507+216_507+224delinsATGGTGGCT
XR_933923.1:n.507+216_507+224delinsATGGTGGCT
NM_001363749.1:c.187+216_187+224delinsATGGTGGCT	NP_001350678.1:n.187+216_187+224delinsATGGTGGCT
NM_001893.5:c.187+216_187+224delinsATGGTGGCT	NP_001884.2:n.187+216_187+224delinsATGGTGGCT
NM_139062.3:c.187+216_187+224delinsATGGTGGCT	NP_620693.1:n.187+216_187+224delinsATGGTGGCT
NR_110578.2:n.556+216_556+224delinsATGGTGGCT
XM_005256336.4:c.187+216_187+224delinsATGGTGGCT	XP_005256393.1:n.187+216_187+224delinsATGGTGGCT
XR_002957961.1:n.506+216_506+224delinsATGGTGGCT
XR_243518.4:n.506+216_506+224delinsATGGTGGCT
XR_430028.4:n.506+216_506+224delinsATGGTGGCT
XR_933922.3:n.506+216_506+224delinsATGGTGGCT
XR_933923.3:n.506+216_506+224delinsATGGTGGCT
NM_001363749.2:c.187+216_187+224delinsATGGTGGCT	NP_001350678.1:n.187+216_187+224delinsATGGTGGCT
NM_001893.6:c.187+216_187+224delinsATGGTGGCT MANE Select	NP_001884.2:n.187+216_187+224delinsATGGTGGCT
NM_139062.4:c.187+216_187+224delinsATGGTGGCT	NP_620693.1:n.187+216_187+224delinsATGGTGGCT