Canonical Allele Identifier: CA2278930004
Gene: CSNK1D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82265656G= , CM000679.2:g.82265656G= GRCh38
NC_000017.10:g.80223532G= , CM000679.1:g.80223532G= GRCh37
NC_000017.9:g.77816821G= NCBI36
NG_012828.1:g.13042C=
NG_012828.2:g.13087C=

Transcript Alleles

HGVS Amino-acid change
ENST00000392334.7:c.187+30C= ENSP00000376146.2:n.187+30C=
ENST00000314028.11:c.187+30C= MANE Select ENSP00000324464.6:n.187+30C=
ENST00000314028.10:c.187+30C= ENSP00000324464.6:n.187+30C=
ENST00000392334.6:c.187+30C= ENSP00000376146.2:n.187+30C=
ENST00000398519.9:c.187+30C= ENSP00000381531.5:n.187+30C=
ENST00000403276.7:c.187+30C= ENSP00000385769.3:n.187+30C=
ENST00000578194.5:n.393+30C=
ENST00000579308.1:n.242C=
ENST00000579316.5:n.244+30C=
ENST00000580061.5:n.187+30C=
ENST00000580446.1:c.76+7650C= ENSP00000463757.1:n.76+7650C=
ENST00000581241.5:n.175+30C=
ENST00000581660.5:c.*225+30C= ENSP00000464551.1:n.*225+30C=
ENST00000582844.5:n.145+30C=
ENST00000584472.5:n.272+30C=
ENST00000585026.1:c.*233+30C= ENSP00000462144.1:n.*233+30C=
NM_001893.4:c.187+30C= NP_001884.2:n.187+30C=
NM_139062.2:c.187+30C= NP_620693.1:n.187+30C=
NR_110578.1:n.548+30C=
XM_005256336.2:c.187+30C= XP_005256393.1:n.187+30C=
XM_005256337.3:c.187+30C= XP_005256394.1:n.187+30C=
XR_243518.2:n.507+30C=
XR_430028.2:n.507+30C=
XR_933922.1:n.507+30C=
XR_933923.1:n.507+30C=
NM_001363749.1:c.187+30C= NP_001350678.1:n.187+30C=
NM_001893.5:c.187+30C= NP_001884.2:n.187+30C=
NM_139062.3:c.187+30C= NP_620693.1:n.187+30C=
NR_110578.2:n.556+30C=
XM_005256336.4:c.187+30C= XP_005256393.1:n.187+30C=
XR_002957961.1:n.506+30C=
XR_243518.4:n.506+30C=
XR_430028.4:n.506+30C=
XR_933922.3:n.506+30C=
XR_933923.3:n.506+30C=
NM_001363749.2:c.187+30C= NP_001350678.1:n.187+30C=
NM_001893.6:c.187+30C= MANE Select NP_001884.2:n.187+30C=
NM_139062.4:c.187+30C= NP_620693.1:n.187+30C=