Canonical Allele Identifier: CA2278930057
Gene: CSNK1D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82265794T= , CM000679.2:g.82265794T= GRCh38
NC_000017.10:g.80223670T= , CM000679.1:g.80223670T= GRCh37
NC_000017.9:g.77816959T= NCBI36
NG_012828.1:g.12904A=
NG_012828.2:g.12949A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392334.7:c.79A= ENSP00000376146.2:p.Thr27=
ENST00000314028.11:c.79A= MANE Select ENSP00000324464.6:p.Thr27=
ENST00000314028.10:c.79A= ENSP00000324464.6:p.Thr27=
ENST00000392334.6:c.79A= ENSP00000376146.2:p.Thr27=
ENST00000398519.9:c.79A= ENSP00000381531.5:p.Thr27=
ENST00000403276.7:c.79A= ENSP00000385769.3:p.Thr27=
ENST00000578194.5:n.285A=
ENST00000579308.1:n.104A=
ENST00000579316.5:n.136A=
ENST00000580061.5:n.79A=
ENST00000580446.1:c.76+7512A= ENSP00000463757.1:n.76+7512A=
ENST00000581241.5:n.67A=
ENST00000581660.5:c.*117A= ENSP00000464551.1:n.*117A=
ENST00000582844.5:n.37A=
ENST00000584472.5:n.164A=
ENST00000585026.1:c.*125A= ENSP00000462144.1:n.*125A=
NM_001893.4:c.79A= NP_001884.2:p.Thr27=
NM_139062.2:c.79A= NP_620693.1:p.Thr27=
NR_110578.1:n.440A=
XM_005256336.2:c.79A= XP_005256393.1:p.Thr27=
XM_005256337.3:c.79A= XP_005256394.1:p.Thr27=
XR_243518.2:n.399A=
XR_430028.2:n.399A=
XR_933922.1:n.399A=
XR_933923.1:n.399A=
NM_001363749.1:c.79A= NP_001350678.1:p.Thr27=
NM_001893.5:c.79A= NP_001884.2:p.Thr27=
NM_139062.3:c.79A= NP_620693.1:p.Thr27=
NR_110578.2:n.448A=
XM_005256336.4:c.79A= XP_005256393.1:p.Thr27=
XR_002957961.1:n.398A=
XR_243518.4:n.398A=
XR_430028.4:n.398A=
XR_933922.3:n.398A=
XR_933923.3:n.398A=
NM_001363749.2:c.79A= NP_001350678.1:p.Thr27=
NM_001893.6:c.79A= MANE Select NP_001884.2:p.Thr27=
NM_139062.4:c.79A= NP_620693.1:p.Thr27=