Canonical Allele Identifier: CA2278930055

Gene: CSNK1D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265790T= , CM000679.2:g.82265790T=	GRCh38
NC_000017.10:g.80223666T= , CM000679.1:g.80223666T=	GRCh37
NC_000017.9:g.77816955T=	NCBI36
NG_012828.1:g.12908A=
NG_012828.2:g.12953A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.83A=	ENSP00000376146.2:p.Asp28=
ENST00000314028.11:c.83A= MANE Select	ENSP00000324464.6:p.Asp28=
ENST00000314028.10:c.83A=	ENSP00000324464.6:p.Asp28=
ENST00000392334.6:c.83A=	ENSP00000376146.2:p.Asp28=
ENST00000398519.9:c.83A=	ENSP00000381531.5:p.Asp28=
ENST00000403276.7:c.83A=	ENSP00000385769.3:p.Asp28=
ENST00000578194.5:n.289A=
ENST00000579308.1:n.108A=
ENST00000579316.5:n.140A=
ENST00000580061.5:n.83A=
ENST00000580446.1:c.76+7516A=	ENSP00000463757.1:n.76+7516A=
ENST00000581241.5:n.71A=
ENST00000581660.5:c.*121A=	ENSP00000464551.1:n.*121A=
ENST00000582844.5:n.41A=
ENST00000584472.5:n.168A=
ENST00000585026.1:c.*129A=	ENSP00000462144.1:n.*129A=
NM_001893.4:c.83A=	NP_001884.2:p.Asp28=
NM_139062.2:c.83A=	NP_620693.1:p.Asp28=
NR_110578.1:n.444A=
XM_005256336.2:c.83A=	XP_005256393.1:p.Asp28=
XM_005256337.3:c.83A=	XP_005256394.1:p.Asp28=
XR_243518.2:n.403A=
XR_430028.2:n.403A=
XR_933922.1:n.403A=
XR_933923.1:n.403A=
NM_001363749.1:c.83A=	NP_001350678.1:p.Asp28=
NM_001893.5:c.83A=	NP_001884.2:p.Asp28=
NM_139062.3:c.83A=	NP_620693.1:p.Asp28=
NR_110578.2:n.452A=
XM_005256336.4:c.83A=	XP_005256393.1:p.Asp28=
XR_002957961.1:n.402A=
XR_243518.4:n.402A=
XR_430028.4:n.402A=
XR_933922.3:n.402A=
XR_933923.3:n.402A=
NM_001363749.2:c.83A=	NP_001350678.1:p.Asp28=
NM_001893.6:c.83A= MANE Select	NP_001884.2:p.Asp28=
NM_139062.4:c.83A=	NP_620693.1:p.Asp28=