Canonical Allele Identifier: CA2278930045

Gene: CSNK1D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265761T= , CM000679.2:g.82265761T=	GRCh38
NC_000017.10:g.80223637T= , CM000679.1:g.80223637T=	GRCh37
NC_000017.9:g.77816926T=	NCBI36
NG_012828.1:g.12937A=
NG_012828.2:g.12982A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.112A=	ENSP00000376146.2:p.Lys38=
ENST00000314028.11:c.112A= MANE Select	ENSP00000324464.6:p.Lys38=
ENST00000314028.10:c.112A=	ENSP00000324464.6:p.Lys38=
ENST00000392334.6:c.112A=	ENSP00000376146.2:p.Lys38=
ENST00000398519.9:c.112A=	ENSP00000381531.5:p.Lys38=
ENST00000403276.7:c.112A=	ENSP00000385769.3:p.Lys38=
ENST00000578194.5:n.318A=
ENST00000579308.1:n.137A=
ENST00000579316.5:n.169A=
ENST00000580061.5:n.112A=
ENST00000580446.1:c.76+7545A=	ENSP00000463757.1:n.76+7545A=
ENST00000581241.5:n.100A=
ENST00000581660.5:c.*150A=	ENSP00000464551.1:n.*150A=
ENST00000582844.5:n.70A=
ENST00000584472.5:n.197A=
ENST00000585026.1:c.*158A=	ENSP00000462144.1:n.*158A=
NM_001893.4:c.112A=	NP_001884.2:p.Lys38=
NM_139062.2:c.112A=	NP_620693.1:p.Lys38=
NR_110578.1:n.473A=
XM_005256336.2:c.112A=	XP_005256393.1:p.Lys38=
XM_005256337.3:c.112A=	XP_005256394.1:p.Lys38=
XR_243518.2:n.432A=
XR_430028.2:n.432A=
XR_933922.1:n.432A=
XR_933923.1:n.432A=
NM_001363749.1:c.112A=	NP_001350678.1:p.Lys38=
NM_001893.5:c.112A=	NP_001884.2:p.Lys38=
NM_139062.3:c.112A=	NP_620693.1:p.Lys38=
NR_110578.2:n.481A=
XM_005256336.4:c.112A=	XP_005256393.1:p.Lys38=
XR_002957961.1:n.431A=
XR_243518.4:n.431A=
XR_430028.4:n.431A=
XR_933922.3:n.431A=
XR_933923.3:n.431A=
NM_001363749.2:c.112A=	NP_001350678.1:p.Lys38=
NM_001893.6:c.112A= MANE Select	NP_001884.2:p.Lys38=
NM_139062.4:c.112A=	NP_620693.1:p.Lys38=