Canonical Allele Identifier: CA2278930036

Gene: CSNK1D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265735G= , CM000679.2:g.82265735G=	GRCh38
NC_000017.10:g.80223611G= , CM000679.1:g.80223611G=	GRCh37
NC_000017.9:g.77816900G=	NCBI36
NG_012828.1:g.12963C=
NG_012828.2:g.13008C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.138C=	ENSP00000376146.2:p.His46=
ENST00000314028.11:c.138C= MANE Select	ENSP00000324464.6:p.His46=
ENST00000314028.10:c.138C=	ENSP00000324464.6:p.His46=
ENST00000392334.6:c.138C=	ENSP00000376146.2:p.His46=
ENST00000398519.9:c.138C=	ENSP00000381531.5:p.His46=
ENST00000403276.7:c.138C=	ENSP00000385769.3:p.His46=
ENST00000578194.5:n.344C=
ENST00000579308.1:n.163C=
ENST00000579316.5:n.195C=
ENST00000580061.5:n.138C=
ENST00000580446.1:c.76+7571C=	ENSP00000463757.1:n.76+7571C=
ENST00000581241.5:n.126C=
ENST00000581660.5:c.*176C=	ENSP00000464551.1:n.*176C=
ENST00000582844.5:n.96C=
ENST00000584472.5:n.223C=
ENST00000585026.1:c.*184C=	ENSP00000462144.1:n.*184C=
NM_001893.4:c.138C=	NP_001884.2:p.His46=
NM_139062.2:c.138C=	NP_620693.1:p.His46=
NR_110578.1:n.499C=
XM_005256336.2:c.138C=	XP_005256393.1:p.His46=
XM_005256337.3:c.138C=	XP_005256394.1:p.His46=
XR_243518.2:n.458C=
XR_430028.2:n.458C=
XR_933922.1:n.458C=
XR_933923.1:n.458C=
NM_001363749.1:c.138C=	NP_001350678.1:p.His46=
NM_001893.5:c.138C=	NP_001884.2:p.His46=
NM_139062.3:c.138C=	NP_620693.1:p.His46=
NR_110578.2:n.507C=
XM_005256336.4:c.138C=	XP_005256393.1:p.His46=
XR_002957961.1:n.457C=
XR_243518.4:n.457C=
XR_430028.4:n.457C=
XR_933922.3:n.457C=
XR_933923.3:n.457C=
NM_001363749.2:c.138C=	NP_001350678.1:p.His46=
NM_001893.6:c.138C= MANE Select	NP_001884.2:p.His46=
NM_139062.4:c.138C=	NP_620693.1:p.His46=