Canonical Allele Identifier: CA2640621021
Gene: CSNK1D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82265924_82265925insT , CM000679.2:g.82265924_82265925insT GRCh38
NC_000017.10:g.80223800_80223801insT , CM000679.1:g.80223800_80223801insT GRCh37
NC_000017.9:g.77817089_77817090insT NCBI36
NG_012828.1:g.12773_12774insA
NG_012828.2:g.12818_12819insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000392334.7:c.77-129_77-128insA ENSP00000376146.2:n.77-129_77-128insA
ENST00000314028.11:c.77-129_77-128insA MANE Select ENSP00000324464.6:n.77-129_77-128insA
ENST00000314028.10:c.77-129_77-128insA ENSP00000324464.6:n.77-129_77-128insA
ENST00000392334.6:c.77-129_77-128insA ENSP00000376146.2:n.77-129_77-128insA
ENST00000398519.9:c.77-129_77-128insA ENSP00000381531.5:n.77-129_77-128insA
ENST00000403276.7:c.77-129_77-128insA ENSP00000385769.3:n.77-129_77-128insA
ENST00000578194.5:n.283-129_283-128insA
ENST00000579308.1:n.102-129_102-128insA
ENST00000579316.5:n.134-129_134-128insA
ENST00000580061.5:n.77-129_77-128insA
ENST00000580446.1:c.76+7381_76+7382insA ENSP00000463757.1:n.76+7381_76+7382insA
ENST00000581241.5:n.65-129_65-128insA
ENST00000581660.5:c.*115-129_*115-128insA ENSP00000464551.1:n.*115-129_*115-128insA
ENST00000582844.5:n.35-129_35-128insA
ENST00000584472.5:n.162-129_162-128insA
ENST00000585026.1:c.*123-129_*123-128insA ENSP00000462144.1:n.*123-129_*123-128insA
NM_001893.4:c.77-129_77-128insA NP_001884.2:n.77-129_77-128insA
NM_139062.2:c.77-129_77-128insA NP_620693.1:n.77-129_77-128insA
NR_110578.1:n.438-129_438-128insA
XM_005256336.2:c.77-129_77-128insA XP_005256393.1:n.77-129_77-128insA
XM_005256337.3:c.77-129_77-128insA XP_005256394.1:n.77-129_77-128insA
XR_243518.2:n.397-129_397-128insA
XR_430028.2:n.397-129_397-128insA
XR_933922.1:n.397-129_397-128insA
XR_933923.1:n.397-129_397-128insA
NM_001363749.1:c.77-129_77-128insA NP_001350678.1:n.77-129_77-128insA
NM_001893.5:c.77-129_77-128insA NP_001884.2:n.77-129_77-128insA
NM_139062.3:c.77-129_77-128insA NP_620693.1:n.77-129_77-128insA
NR_110578.2:n.446-129_446-128insA
XM_005256336.4:c.77-129_77-128insA XP_005256393.1:n.77-129_77-128insA
XR_002957961.1:n.396-129_396-128insA
XR_243518.4:n.396-129_396-128insA
XR_430028.4:n.396-129_396-128insA
XR_933922.3:n.396-129_396-128insA
XR_933923.3:n.396-129_396-128insA
NM_001363749.2:c.77-129_77-128insA NP_001350678.1:n.77-129_77-128insA
NM_001893.6:c.77-129_77-128insA MANE Select NP_001884.2:n.77-129_77-128insA
NM_139062.4:c.77-129_77-128insA NP_620693.1:n.77-129_77-128insA