Canonical Allele Identifier: CA401597138

Gene: CSNK1D

Linked Data

• MyVariant Identifiers: chr17:g.80223655C>G (hg19) ; chr17:g.82265779C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265779C>G , CM000679.2:g.82265779C>G	GRCh38
NC_000017.10:g.80223655C>G , CM000679.1:g.80223655C>G	GRCh37
NC_000017.9:g.77816944C>G	NCBI36
NG_012828.1:g.12919G>C
NG_012828.2:g.12964G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.94G>C	ENSP00000376146.2:p.Gly32Arg
ENST00000314028.11:c.94G>C MANE Select	ENSP00000324464.6:p.Gly32Arg
ENST00000314028.10:c.94G>C	ENSP00000324464.6:p.Gly32Arg
ENST00000392334.6:c.94G>C	ENSP00000376146.2:p.Gly32Arg
ENST00000398519.9:c.94G>C	ENSP00000381531.5:p.Gly32Arg
ENST00000403276.7:c.94G>C	ENSP00000385769.3:p.Gly32Arg
ENST00000578194.5:n.300G>C
ENST00000579308.1:n.119G>C
ENST00000579316.5:n.151G>C
ENST00000580061.5:n.94G>C
ENST00000580446.1:c.76+7527G>C	ENSP00000463757.1:n.76+7527G>C
ENST00000581241.5:n.82G>C
ENST00000581660.5:c.*132G>C	ENSP00000464551.1:n.*132G>C
ENST00000582844.5:n.52G>C
ENST00000584472.5:n.179G>C
ENST00000585026.1:c.*140G>C	ENSP00000462144.1:n.*140G>C
NM_001893.4:c.94G>C	NP_001884.2:p.Gly32Arg
NM_139062.2:c.94G>C	NP_620693.1:p.Gly32Arg
NR_110578.1:n.455G>C
XM_005256336.2:c.94G>C	XP_005256393.1:p.Gly32Arg
XM_005256337.3:c.94G>C	XP_005256394.1:p.Gly32Arg
XR_243518.2:n.414G>C
XR_430028.2:n.414G>C
XR_933922.1:n.414G>C
XR_933923.1:n.414G>C
NM_001363749.1:c.94G>C	NP_001350678.1:p.Gly32Arg
NM_001893.5:c.94G>C	NP_001884.2:p.Gly32Arg
NM_139062.3:c.94G>C	NP_620693.1:p.Gly32Arg
NR_110578.2:n.463G>C
XM_005256336.4:c.94G>C	XP_005256393.1:p.Gly32Arg
XR_002957961.1:n.413G>C
XR_243518.4:n.413G>C
XR_430028.4:n.413G>C
XR_933922.3:n.413G>C
XR_933923.3:n.413G>C
NM_001363749.2:c.94G>C	NP_001350678.1:p.Gly32Arg
NM_001893.6:c.94G>C MANE Select	NP_001884.2:p.Gly32Arg
NM_139062.4:c.94G>C	NP_620693.1:p.Gly32Arg