Canonical Allele Identifier: CA2640619856

Gene: CSNK1D

Linked Data

• gnomAD v4: 17-82265490-TCTTTGTGTTGAGGGAGGGTCTCTGGACCCAAGACTCTCTGAAGGAAGCTGTGACTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265497_82265552del , CM000679.2:g.82265497_82265552del	GRCh38
NC_000017.10:g.80223373_80223428del , CM000679.1:g.80223373_80223428del	GRCh37
NC_000017.9:g.77816662_77816717del	NCBI36
NG_012828.1:g.13152_13207del
NG_012828.2:g.13197_13252del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.187+140_187+195del	ENSP00000376146.2:n.187+140_187+195del
ENST00000314028.11:c.187+140_187+195del MANE Select	ENSP00000324464.6:n.187+140_187+195del
ENST00000314028.10:c.187+140_187+195del	ENSP00000324464.6:n.187+140_187+195del
ENST00000392334.6:c.187+140_187+195del	ENSP00000376146.2:n.187+140_187+195del
ENST00000398519.9:c.187+140_187+195del	ENSP00000381531.5:n.187+140_187+195del
ENST00000403276.7:c.187+140_187+195del	ENSP00000385769.3:n.187+140_187+195del
ENST00000578194.5:n.393+140_393+195del
ENST00000579308.1:n.352_407del
ENST00000579316.5:n.244+140_244+195del
ENST00000580061.5:n.187+140_187+195del
ENST00000580446.1:c.76+7760_76+7815del	ENSP00000463757.1:n.76+7760_76+7815del
ENST00000581241.5:n.175+140_175+195del
ENST00000581660.5:c.*225+140_*225+195del	ENSP00000464551.1:n.*225+140_*225+195del
ENST00000582844.5:n.145+140_145+195del
ENST00000584472.5:n.272+140_272+195del
ENST00000585026.1:c.*233+140_*233+195del	ENSP00000462144.1:n.*233+140_*233+195del
NM_001893.4:c.187+140_187+195del	NP_001884.2:n.187+140_187+195del
NM_139062.2:c.187+140_187+195del	NP_620693.1:n.187+140_187+195del
NR_110578.1:n.548+140_548+195del
XM_005256336.2:c.187+140_187+195del	XP_005256393.1:n.187+140_187+195del
XM_005256337.3:c.187+140_187+195del	XP_005256394.1:n.187+140_187+195del
XR_243518.2:n.507+140_507+195del
XR_430028.2:n.507+140_507+195del
XR_933922.1:n.507+140_507+195del
XR_933923.1:n.507+140_507+195del
NM_001363749.1:c.187+140_187+195del	NP_001350678.1:n.187+140_187+195del
NM_001893.5:c.187+140_187+195del	NP_001884.2:n.187+140_187+195del
NM_139062.3:c.187+140_187+195del	NP_620693.1:n.187+140_187+195del
NR_110578.2:n.556+140_556+195del
XM_005256336.4:c.187+140_187+195del	XP_005256393.1:n.187+140_187+195del
XR_002957961.1:n.506+140_506+195del
XR_243518.4:n.506+140_506+195del
XR_430028.4:n.506+140_506+195del
XR_933922.3:n.506+140_506+195del
XR_933923.3:n.506+140_506+195del
NM_001363749.2:c.187+140_187+195del	NP_001350678.1:n.187+140_187+195del
NM_001893.6:c.187+140_187+195del MANE Select	NP_001884.2:n.187+140_187+195del
NM_139062.4:c.187+140_187+195del	NP_620693.1:n.187+140_187+195del