Canonical Allele Identifier: CA914214525

Gene: CSNK1D

Linked Data

• dbSNP Id: rs1568582244
• gnomAD v2: 17-80223367-CTTT-C
• gnomAD v3: 17-82265491-CTTT-C
• gnomAD v4: 17-82265491-CTTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265492_82265494del , CM000679.2:g.82265492_82265494del	GRCh38
NC_000017.10:g.80223368_80223370del , CM000679.1:g.80223368_80223370del	GRCh37
NC_000017.9:g.77816657_77816659del	NCBI36
NG_012828.1:g.13204_13206del
NG_012828.2:g.13249_13251del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.187+192_187+194del	ENSP00000376146.2:n.187+192_187+194del
ENST00000314028.11:c.187+192_187+194del MANE Select	ENSP00000324464.6:n.187+192_187+194del
ENST00000314028.10:c.187+192_187+194del	ENSP00000324464.6:n.187+192_187+194del
ENST00000392334.6:c.187+192_187+194del	ENSP00000376146.2:n.187+192_187+194del
ENST00000398519.9:c.187+192_187+194del	ENSP00000381531.5:n.187+192_187+194del
ENST00000403276.7:c.187+192_187+194del	ENSP00000385769.3:n.187+192_187+194del
ENST00000578194.5:n.393+192_393+194del
ENST00000579308.1:n.404_406del
ENST00000579316.5:n.244+192_244+194del
ENST00000580061.5:n.187+192_187+194del
ENST00000580446.1:c.76+7812_76+7814del	ENSP00000463757.1:n.76+7812_76+7814del
ENST00000581241.5:n.175+192_175+194del
ENST00000581660.5:c.*225+192_*225+194del	ENSP00000464551.1:n.*225+192_*225+194del
ENST00000582844.5:n.145+192_145+194del
ENST00000584472.5:n.272+192_272+194del
ENST00000585026.1:c.*233+192_*233+194del	ENSP00000462144.1:n.*233+192_*233+194del
NM_001893.4:c.187+192_187+194del	NP_001884.2:n.187+192_187+194del
NM_139062.2:c.187+192_187+194del	NP_620693.1:n.187+192_187+194del
NR_110578.1:n.548+192_548+194del
XM_005256336.2:c.187+192_187+194del	XP_005256393.1:n.187+192_187+194del
XM_005256337.3:c.187+192_187+194del	XP_005256394.1:n.187+192_187+194del
XR_243518.2:n.507+192_507+194del
XR_430028.2:n.507+192_507+194del
XR_933922.1:n.507+192_507+194del
XR_933923.1:n.507+192_507+194del
NM_001363749.1:c.187+192_187+194del	NP_001350678.1:n.187+192_187+194del
NM_001893.5:c.187+192_187+194del	NP_001884.2:n.187+192_187+194del
NM_139062.3:c.187+192_187+194del	NP_620693.1:n.187+192_187+194del
NR_110578.2:n.556+192_556+194del
XM_005256336.4:c.187+192_187+194del	XP_005256393.1:n.187+192_187+194del
XR_002957961.1:n.506+192_506+194del
XR_243518.4:n.506+192_506+194del
XR_430028.4:n.506+192_506+194del
XR_933922.3:n.506+192_506+194del
XR_933923.3:n.506+192_506+194del
NM_001363749.2:c.187+192_187+194del	NP_001350678.1:n.187+192_187+194del
NM_001893.6:c.187+192_187+194del MANE Select	NP_001884.2:n.187+192_187+194del
NM_139062.4:c.187+192_187+194del	NP_620693.1:n.187+192_187+194del