Canonical Allele Identifier: CA143736
Gene: CSNK1D HGNC NCBI

Linked Data

ClinVar Variation Id: 50319
ClinVar RCV Id: RCV000043507
dbSNP Id: rs397514693

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82265736T>C , CM000679.2:g.82265736T>C GRCh38
NC_000017.10:g.80223612T>C , CM000679.1:g.80223612T>C GRCh37
NC_000017.9:g.77816901T>C NCBI36
NG_012828.1:g.12962A>G
NG_012828.2:g.13007A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000392334.7:c.137A>G ENSP00000376146.2:p.His46Arg
ENST00000314028.11:c.137A>G MANE Select ENSP00000324464.6:p.His46Arg
ENST00000314028.10:c.137A>G ENSP00000324464.6:p.His46Arg
ENST00000392334.6:c.137A>G ENSP00000376146.2:p.His46Arg
ENST00000398519.9:c.137A>G ENSP00000381531.5:p.His46Arg
ENST00000403276.7:c.137A>G ENSP00000385769.3:p.His46Arg
ENST00000578194.5:n.343A>G
ENST00000579308.1:n.162A>G
ENST00000579316.5:n.194A>G
ENST00000580061.5:n.137A>G
ENST00000580446.1:c.76+7570A>G ENSP00000463757.1:n.76+7570A>G
ENST00000581241.5:n.125A>G
ENST00000581660.5:c.*175A>G ENSP00000464551.1:n.*175A>G
ENST00000582844.5:n.95A>G
ENST00000584472.5:n.222A>G
ENST00000585026.1:c.*183A>G ENSP00000462144.1:n.*183A>G
NM_001893.4:c.137A>G NP_001884.2:p.His46Arg
NM_139062.2:c.137A>G NP_620693.1:p.His46Arg
NR_110578.1:n.498A>G
XM_005256336.2:c.137A>G XP_005256393.1:p.His46Arg
XM_005256337.3:c.137A>G XP_005256394.1:p.His46Arg
XR_243518.2:n.457A>G
XR_430028.2:n.457A>G
XR_933922.1:n.457A>G
XR_933923.1:n.457A>G
NM_001363749.1:c.137A>G NP_001350678.1:p.His46Arg
NM_001893.5:c.137A>G NP_001884.2:p.His46Arg
NM_139062.3:c.137A>G NP_620693.1:p.His46Arg
NR_110578.2:n.506A>G
XM_005256336.4:c.137A>G XP_005256393.1:p.His46Arg
XR_002957961.1:n.456A>G
XR_243518.4:n.456A>G
XR_430028.4:n.456A>G
XR_933922.3:n.456A>G
XR_933923.3:n.456A>G
NM_001363749.2:c.137A>G NP_001350678.1:p.His46Arg
NM_001893.6:c.137A>G MANE Select NP_001884.2:p.His46Arg
NM_139062.4:c.137A>G NP_620693.1:p.His46Arg