Canonical Allele Identifier: CA2278930029
Gene: CSNK1D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82265700A= , CM000679.2:g.82265700A= GRCh38
NC_000017.10:g.80223576A= , CM000679.1:g.80223576A= GRCh37
NC_000017.9:g.77816865A= NCBI36
NG_012828.1:g.12998T=
NG_012828.2:g.13043T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392334.7:c.173T= ENSP00000376146.2:p.Met58=
ENST00000314028.11:c.173T= MANE Select ENSP00000324464.6:p.Met58=
ENST00000314028.10:c.173T= ENSP00000324464.6:p.Met58=
ENST00000392334.6:c.173T= ENSP00000376146.2:p.Met58=
ENST00000398519.9:c.173T= ENSP00000381531.5:p.Met58=
ENST00000403276.7:c.173T= ENSP00000385769.3:p.Met58=
ENST00000578194.5:n.379T=
ENST00000579308.1:n.198T=
ENST00000579316.5:n.230T=
ENST00000580061.5:n.173T=
ENST00000580446.1:c.76+7606T= ENSP00000463757.1:n.76+7606T=
ENST00000581241.5:n.161T=
ENST00000581660.5:c.*211T= ENSP00000464551.1:n.*211T=
ENST00000582844.5:n.131T=
ENST00000584472.5:n.258T=
ENST00000585026.1:c.*219T= ENSP00000462144.1:n.*219T=
NM_001893.4:c.173T= NP_001884.2:p.Met58=
NM_139062.2:c.173T= NP_620693.1:p.Met58=
NR_110578.1:n.534T=
XM_005256336.2:c.173T= XP_005256393.1:p.Met58=
XM_005256337.3:c.173T= XP_005256394.1:p.Met58=
XR_243518.2:n.493T=
XR_430028.2:n.493T=
XR_933922.1:n.493T=
XR_933923.1:n.493T=
NM_001363749.1:c.173T= NP_001350678.1:p.Met58=
NM_001893.5:c.173T= NP_001884.2:p.Met58=
NM_139062.3:c.173T= NP_620693.1:p.Met58=
NR_110578.2:n.542T=
XM_005256336.4:c.173T= XP_005256393.1:p.Met58=
XR_002957961.1:n.492T=
XR_243518.4:n.492T=
XR_430028.4:n.492T=
XR_933922.3:n.492T=
XR_933923.3:n.492T=
NM_001363749.2:c.173T= NP_001350678.1:p.Met58=
NM_001893.6:c.173T= MANE Select NP_001884.2:p.Met58=
NM_139062.4:c.173T= NP_620693.1:p.Met58=