Canonical Allele Identifier: CA2278930042
Gene: CSNK1D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82265753T= , CM000679.2:g.82265753T= GRCh38
NC_000017.10:g.80223629T= , CM000679.1:g.80223629T= GRCh37
NC_000017.9:g.77816918T= NCBI36
NG_012828.1:g.12945A=
NG_012828.2:g.12990A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392334.7:c.120A= ENSP00000376146.2:p.Glu40=
ENST00000314028.11:c.120A= MANE Select ENSP00000324464.6:p.Glu40=
ENST00000314028.10:c.120A= ENSP00000324464.6:p.Glu40=
ENST00000392334.6:c.120A= ENSP00000376146.2:p.Glu40=
ENST00000398519.9:c.120A= ENSP00000381531.5:p.Glu40=
ENST00000403276.7:c.120A= ENSP00000385769.3:p.Glu40=
ENST00000578194.5:n.326A=
ENST00000579308.1:n.145A=
ENST00000579316.5:n.177A=
ENST00000580061.5:n.120A=
ENST00000580446.1:c.76+7553A= ENSP00000463757.1:n.76+7553A=
ENST00000581241.5:n.108A=
ENST00000581660.5:c.*158A= ENSP00000464551.1:n.*158A=
ENST00000582844.5:n.78A=
ENST00000584472.5:n.205A=
ENST00000585026.1:c.*166A= ENSP00000462144.1:n.*166A=
NM_001893.4:c.120A= NP_001884.2:p.Glu40=
NM_139062.2:c.120A= NP_620693.1:p.Glu40=
NR_110578.1:n.481A=
XM_005256336.2:c.120A= XP_005256393.1:p.Glu40=
XM_005256337.3:c.120A= XP_005256394.1:p.Glu40=
XR_243518.2:n.440A=
XR_430028.2:n.440A=
XR_933922.1:n.440A=
XR_933923.1:n.440A=
NM_001363749.1:c.120A= NP_001350678.1:p.Glu40=
NM_001893.5:c.120A= NP_001884.2:p.Glu40=
NM_139062.3:c.120A= NP_620693.1:p.Glu40=
NR_110578.2:n.489A=
XM_005256336.4:c.120A= XP_005256393.1:p.Glu40=
XR_002957961.1:n.439A=
XR_243518.4:n.439A=
XR_430028.4:n.439A=
XR_933922.3:n.439A=
XR_933923.3:n.439A=
NM_001363749.2:c.120A= NP_001350678.1:p.Glu40=
NM_001893.6:c.120A= MANE Select NP_001884.2:p.Glu40=
NM_139062.4:c.120A= NP_620693.1:p.Glu40=