Canonical Allele Identifier: CA401596893

Gene: CSNK1D

Linked Data

• dbSNP Id: rs1599615072
• MyVariant Identifiers: chr17:g.80223606T>C (hg19) ; chr17:g.82265730T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265730T>C , CM000679.2:g.82265730T>C	GRCh38
NC_000017.10:g.80223606T>C , CM000679.1:g.80223606T>C	GRCh37
NC_000017.9:g.77816895T>C	NCBI36
NG_012828.1:g.12968A>G
NG_012828.2:g.13013A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.143A>G	ENSP00000376146.2:p.Gln48Arg
ENST00000314028.11:c.143A>G MANE Select	ENSP00000324464.6:p.Gln48Arg
ENST00000314028.10:c.143A>G	ENSP00000324464.6:p.Gln48Arg
ENST00000392334.6:c.143A>G	ENSP00000376146.2:p.Gln48Arg
ENST00000398519.9:c.143A>G	ENSP00000381531.5:p.Gln48Arg
ENST00000403276.7:c.143A>G	ENSP00000385769.3:p.Gln48Arg
ENST00000578194.5:n.349A>G
ENST00000579308.1:n.168A>G
ENST00000579316.5:n.200A>G
ENST00000580061.5:n.143A>G
ENST00000580446.1:c.76+7576A>G	ENSP00000463757.1:n.76+7576A>G
ENST00000581241.5:n.131A>G
ENST00000581660.5:c.*181A>G	ENSP00000464551.1:n.*181A>G
ENST00000582844.5:n.101A>G
ENST00000584472.5:n.228A>G
ENST00000585026.1:c.*189A>G	ENSP00000462144.1:n.*189A>G
NM_001893.4:c.143A>G	NP_001884.2:p.Gln48Arg
NM_139062.2:c.143A>G	NP_620693.1:p.Gln48Arg
NR_110578.1:n.504A>G
XM_005256336.2:c.143A>G	XP_005256393.1:p.Gln48Arg
XM_005256337.3:c.143A>G	XP_005256394.1:p.Gln48Arg
XR_243518.2:n.463A>G
XR_430028.2:n.463A>G
XR_933922.1:n.463A>G
XR_933923.1:n.463A>G
NM_001363749.1:c.143A>G	NP_001350678.1:p.Gln48Arg
NM_001893.5:c.143A>G	NP_001884.2:p.Gln48Arg
NM_139062.3:c.143A>G	NP_620693.1:p.Gln48Arg
NR_110578.2:n.512A>G
XM_005256336.4:c.143A>G	XP_005256393.1:p.Gln48Arg
XR_002957961.1:n.462A>G
XR_243518.4:n.462A>G
XR_430028.4:n.462A>G
XR_933922.3:n.462A>G
XR_933923.3:n.462A>G
NM_001363749.2:c.143A>G	NP_001350678.1:p.Gln48Arg
NM_001893.6:c.143A>G MANE Select	NP_001884.2:p.Gln48Arg
NM_139062.4:c.143A>G	NP_620693.1:p.Gln48Arg