Canonical Allele Identifier: CA2640619050

Gene: CSNK1D

Linked Data

• gnomAD v4: 17-82265265-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265267del , CM000679.2:g.82265267del	GRCh38
NC_000017.10:g.80223143del , CM000679.1:g.80223143del	GRCh37
NC_000017.9:g.77816432del	NCBI36
NG_012828.1:g.13432del
NG_012828.2:g.13477del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.187+420del	ENSP00000376146.2:n.187+420del
ENST00000314028.11:c.187+420del MANE Select	ENSP00000324464.6:n.187+420del
ENST00000314028.10:c.187+420del	ENSP00000324464.6:n.187+420del
ENST00000392334.6:c.187+420del	ENSP00000376146.2:n.187+420del
ENST00000398519.9:c.187+420del	ENSP00000381531.5:n.187+420del
ENST00000403276.7:c.187+420del	ENSP00000385769.3:n.187+420del
ENST00000578194.5:n.393+420del
ENST00000579316.5:n.244+420del
ENST00000580061.5:n.187+420del
ENST00000580446.1:c.76+8040del	ENSP00000463757.1:n.76+8040del
ENST00000581241.5:n.175+420del
ENST00000581660.5:c.*225+420del	ENSP00000464551.1:n.*225+420del
ENST00000582844.5:n.145+420del
ENST00000584472.5:n.272+420del
ENST00000585026.1:c.*233+420del	ENSP00000462144.1:n.*233+420del
NM_001893.4:c.187+420del	NP_001884.2:n.187+420del
NM_139062.2:c.187+420del	NP_620693.1:n.187+420del
NR_110578.1:n.548+420del
XM_005256336.2:c.187+420del	XP_005256393.1:n.187+420del
XM_005256337.3:c.187+420del	XP_005256394.1:n.187+420del
XR_243518.2:n.507+420del
XR_430028.2:n.507+420del
XR_933922.1:n.507+420del
XR_933923.1:n.507+420del
NM_001363749.1:c.187+420del	NP_001350678.1:n.187+420del
NM_001893.5:c.187+420del	NP_001884.2:n.187+420del
NM_139062.3:c.187+420del	NP_620693.1:n.187+420del
NR_110578.2:n.556+420del
XM_005256336.4:c.187+420del	XP_005256393.1:n.187+420del
XR_002957961.1:n.506+420del
XR_243518.4:n.506+420del
XR_430028.4:n.506+420del
XR_933922.3:n.506+420del
XR_933923.3:n.506+420del
NM_001363749.2:c.187+420del	NP_001350678.1:n.187+420del
NM_001893.6:c.187+420del MANE Select	NP_001884.2:n.187+420del
NM_139062.4:c.187+420del	NP_620693.1:n.187+420del