Canonical Allele Identifier: CA2640619059

Gene: CSNK1D

Linked Data

• gnomAD v4: 17-82265270-C-CCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265271_82265272dup , CM000679.2:g.82265271_82265272dup	GRCh38
NC_000017.10:g.80223147_80223148dup , CM000679.1:g.80223147_80223148dup	GRCh37
NC_000017.9:g.77816436_77816437dup	NCBI36
NG_012828.1:g.13426_13427dup
NG_012828.2:g.13471_13472dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.187+414_187+415dup	ENSP00000376146.2:n.187+414_187+415dup
ENST00000314028.11:c.187+414_187+415dup MANE Select	ENSP00000324464.6:n.187+414_187+415dup
ENST00000314028.10:c.187+414_187+415dup	ENSP00000324464.6:n.187+414_187+415dup
ENST00000392334.6:c.187+414_187+415dup	ENSP00000376146.2:n.187+414_187+415dup
ENST00000398519.9:c.187+414_187+415dup	ENSP00000381531.5:n.187+414_187+415dup
ENST00000403276.7:c.187+414_187+415dup	ENSP00000385769.3:n.187+414_187+415dup
ENST00000578194.5:n.393+414_393+415dup
ENST00000579316.5:n.244+414_244+415dup
ENST00000580061.5:n.187+414_187+415dup
ENST00000580446.1:c.76+8034_76+8035dup	ENSP00000463757.1:n.76+8034_76+8035dup
ENST00000581241.5:n.175+414_175+415dup
ENST00000581660.5:c.*225+414_*225+415dup	ENSP00000464551.1:n.*225+414_*225+415dup
ENST00000582844.5:n.145+414_145+415dup
ENST00000584472.5:n.272+414_272+415dup
ENST00000585026.1:c.*233+414_*233+415dup	ENSP00000462144.1:n.*233+414_*233+415dup
NM_001893.4:c.187+414_187+415dup	NP_001884.2:n.187+414_187+415dup
NM_139062.2:c.187+414_187+415dup	NP_620693.1:n.187+414_187+415dup
NR_110578.1:n.548+414_548+415dup
XM_005256336.2:c.187+414_187+415dup	XP_005256393.1:n.187+414_187+415dup
XM_005256337.3:c.187+414_187+415dup	XP_005256394.1:n.187+414_187+415dup
XR_243518.2:n.507+414_507+415dup
XR_430028.2:n.507+414_507+415dup
XR_933922.1:n.507+414_507+415dup
XR_933923.1:n.507+414_507+415dup
NM_001363749.1:c.187+414_187+415dup	NP_001350678.1:n.187+414_187+415dup
NM_001893.5:c.187+414_187+415dup	NP_001884.2:n.187+414_187+415dup
NM_139062.3:c.187+414_187+415dup	NP_620693.1:n.187+414_187+415dup
NR_110578.2:n.556+414_556+415dup
XM_005256336.4:c.187+414_187+415dup	XP_005256393.1:n.187+414_187+415dup
XR_002957961.1:n.506+414_506+415dup
XR_243518.4:n.506+414_506+415dup
XR_430028.4:n.506+414_506+415dup
XR_933922.3:n.506+414_506+415dup
XR_933923.3:n.506+414_506+415dup
NM_001363749.2:c.187+414_187+415dup	NP_001350678.1:n.187+414_187+415dup
NM_001893.6:c.187+414_187+415dup MANE Select	NP_001884.2:n.187+414_187+415dup
NM_139062.4:c.187+414_187+415dup	NP_620693.1:n.187+414_187+415dup