Canonical Allele Identifier: CA2278930072

Gene: CSNK1D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265822_82265823delinsAG , CM000679.2:g.82265822_82265823delinsAG	GRCh38
NC_000017.10:g.80223698_80223699delinsAG , CM000679.1:g.80223698_80223699delinsAG	GRCh37
NC_000017.9:g.77816987_77816988delinsAG	NCBI36
NG_012828.1:g.12875_12876delinsCT
NG_012828.2:g.12920_12921delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.77-27_77-26delinsCT	ENSP00000376146.2:n.77-27_77-26delinsCT
ENST00000314028.11:c.77-27_77-26delinsCT MANE Select	ENSP00000324464.6:n.77-27_77-26delinsCT
ENST00000314028.10:c.77-27_77-26delinsCT	ENSP00000324464.6:n.77-27_77-26delinsCT
ENST00000392334.6:c.77-27_77-26delinsCT	ENSP00000376146.2:n.77-27_77-26delinsCT
ENST00000398519.9:c.77-27_77-26delinsCT	ENSP00000381531.5:n.77-27_77-26delinsCT
ENST00000403276.7:c.77-27_77-26delinsCT	ENSP00000385769.3:n.77-27_77-26delinsCT
ENST00000578194.5:n.283-27_283-26delinsCT
ENST00000579308.1:n.102-27_102-26delinsCT
ENST00000579316.5:n.134-27_134-26delinsCT
ENST00000580061.5:n.77-27_77-26delinsCT
ENST00000580446.1:c.76+7483_76+7484delinsCT	ENSP00000463757.1:n.76+7483_76+7484delinsCT
ENST00000581241.5:n.65-27_65-26delinsCT
ENST00000581660.5:c.*115-27_*115-26delinsCT	ENSP00000464551.1:n.*115-27_*115-26delinsCT
ENST00000582844.5:n.35-27_35-26delinsCT
ENST00000584472.5:n.162-27_162-26delinsCT
ENST00000585026.1:c.*123-27_*123-26delinsCT	ENSP00000462144.1:n.*123-27_*123-26delinsCT
NM_001893.4:c.77-27_77-26delinsCT	NP_001884.2:n.77-27_77-26delinsCT
NM_139062.2:c.77-27_77-26delinsCT	NP_620693.1:n.77-27_77-26delinsCT
NR_110578.1:n.438-27_438-26delinsCT
XM_005256336.2:c.77-27_77-26delinsCT	XP_005256393.1:n.77-27_77-26delinsCT
XM_005256337.3:c.77-27_77-26delinsCT	XP_005256394.1:n.77-27_77-26delinsCT
XR_243518.2:n.397-27_397-26delinsCT
XR_430028.2:n.397-27_397-26delinsCT
XR_933922.1:n.397-27_397-26delinsCT
XR_933923.1:n.397-27_397-26delinsCT
NM_001363749.1:c.77-27_77-26delinsCT	NP_001350678.1:n.77-27_77-26delinsCT
NM_001893.5:c.77-27_77-26delinsCT	NP_001884.2:n.77-27_77-26delinsCT
NM_139062.3:c.77-27_77-26delinsCT	NP_620693.1:n.77-27_77-26delinsCT
NR_110578.2:n.446-27_446-26delinsCT
XM_005256336.4:c.77-27_77-26delinsCT	XP_005256393.1:n.77-27_77-26delinsCT
XR_002957961.1:n.396-27_396-26delinsCT
XR_243518.4:n.396-27_396-26delinsCT
XR_430028.4:n.396-27_396-26delinsCT
XR_933922.3:n.396-27_396-26delinsCT
XR_933923.3:n.396-27_396-26delinsCT
NM_001363749.2:c.77-27_77-26delinsCT	NP_001350678.1:n.77-27_77-26delinsCT
NM_001893.6:c.77-27_77-26delinsCT MANE Select	NP_001884.2:n.77-27_77-26delinsCT
NM_139062.4:c.77-27_77-26delinsCT	NP_620693.1:n.77-27_77-26delinsCT