Canonical Allele Identifier: CA775732203

Gene: CSNK1D

Linked Data

• dbSNP Id: rs1345049734
• gnomAD v3: 17-82265462-AGCCACCAT-A
• gnomAD v4: 17-82265462-AGCCACCAT-A
• MyVariant Identifiers: chr17:g.80223339_80223346del (hg19) ; chr17:g.82265463_82265470del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265466_82265473del , CM000679.2:g.82265466_82265473del	GRCh38
NC_000017.10:g.80223342_80223349del , CM000679.1:g.80223342_80223349del	GRCh37
NC_000017.9:g.77816631_77816638del	NCBI36
NG_012828.1:g.13228_13235del
NG_012828.2:g.13273_13280del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.187+216_187+223del	ENSP00000376146.2:n.187+216_187+223del
ENST00000314028.11:c.187+216_187+223del MANE Select	ENSP00000324464.6:n.187+216_187+223del
ENST00000314028.10:c.187+216_187+223del	ENSP00000324464.6:n.187+216_187+223del
ENST00000392334.6:c.187+216_187+223del	ENSP00000376146.2:n.187+216_187+223del
ENST00000398519.9:c.187+216_187+223del	ENSP00000381531.5:n.187+216_187+223del
ENST00000403276.7:c.187+216_187+223del	ENSP00000385769.3:n.187+216_187+223del
ENST00000578194.5:n.393+216_393+223del
ENST00000579308.1:n.428_435del
ENST00000579316.5:n.244+216_244+223del
ENST00000580061.5:n.187+216_187+223del
ENST00000580446.1:c.76+7836_76+7843del	ENSP00000463757.1:n.76+7836_76+7843del
ENST00000581241.5:n.175+216_175+223del
ENST00000581660.5:c.*225+216_*225+223del	ENSP00000464551.1:n.*225+216_*225+223del
ENST00000582844.5:n.145+216_145+223del
ENST00000584472.5:n.272+216_272+223del
ENST00000585026.1:c.*233+216_*233+223del	ENSP00000462144.1:n.*233+216_*233+223del
NM_001893.4:c.187+216_187+223del	NP_001884.2:n.187+216_187+223del
NM_139062.2:c.187+216_187+223del	NP_620693.1:n.187+216_187+223del
NR_110578.1:n.548+216_548+223del
XM_005256336.2:c.187+216_187+223del	XP_005256393.1:n.187+216_187+223del
XM_005256337.3:c.187+216_187+223del	XP_005256394.1:n.187+216_187+223del
XR_243518.2:n.507+216_507+223del
XR_430028.2:n.507+216_507+223del
XR_933922.1:n.507+216_507+223del
XR_933923.1:n.507+216_507+223del
NM_001363749.1:c.187+216_187+223del	NP_001350678.1:n.187+216_187+223del
NM_001893.5:c.187+216_187+223del	NP_001884.2:n.187+216_187+223del
NM_139062.3:c.187+216_187+223del	NP_620693.1:n.187+216_187+223del
NR_110578.2:n.556+216_556+223del
XM_005256336.4:c.187+216_187+223del	XP_005256393.1:n.187+216_187+223del
XR_002957961.1:n.506+216_506+223del
XR_243518.4:n.506+216_506+223del
XR_430028.4:n.506+216_506+223del
XR_933922.3:n.506+216_506+223del
XR_933923.3:n.506+216_506+223del
NM_001363749.2:c.187+216_187+223del	NP_001350678.1:n.187+216_187+223del
NM_001893.6:c.187+216_187+223del MANE Select	NP_001884.2:n.187+216_187+223del
NM_139062.4:c.187+216_187+223del	NP_620693.1:n.187+216_187+223del