Canonical Allele Identifier: CA401596877

Gene: CSNK1D

Linked Data

• MyVariant Identifiers: chr17:g.80223603A>C (hg19) ; chr17:g.82265727A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265727A>C , CM000679.2:g.82265727A>C	GRCh38
NC_000017.10:g.80223603A>C , CM000679.1:g.80223603A>C	GRCh37
NC_000017.9:g.77816892A>C	NCBI36
NG_012828.1:g.12971T>G
NG_012828.2:g.13016T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.146T>G	ENSP00000376146.2:p.Leu49Arg
ENST00000314028.11:c.146T>G MANE Select	ENSP00000324464.6:p.Leu49Arg
ENST00000314028.10:c.146T>G	ENSP00000324464.6:p.Leu49Arg
ENST00000392334.6:c.146T>G	ENSP00000376146.2:p.Leu49Arg
ENST00000398519.9:c.146T>G	ENSP00000381531.5:p.Leu49Arg
ENST00000403276.7:c.146T>G	ENSP00000385769.3:p.Leu49Arg
ENST00000578194.5:n.352T>G
ENST00000579308.1:n.171T>G
ENST00000579316.5:n.203T>G
ENST00000580061.5:n.146T>G
ENST00000580446.1:c.76+7579T>G	ENSP00000463757.1:n.76+7579T>G
ENST00000581241.5:n.134T>G
ENST00000581660.5:c.*184T>G	ENSP00000464551.1:n.*184T>G
ENST00000582844.5:n.104T>G
ENST00000584472.5:n.231T>G
ENST00000585026.1:c.*192T>G	ENSP00000462144.1:n.*192T>G
NM_001893.4:c.146T>G	NP_001884.2:p.Leu49Arg
NM_139062.2:c.146T>G	NP_620693.1:p.Leu49Arg
NR_110578.1:n.507T>G
XM_005256336.2:c.146T>G	XP_005256393.1:p.Leu49Arg
XM_005256337.3:c.146T>G	XP_005256394.1:p.Leu49Arg
XR_243518.2:n.466T>G
XR_430028.2:n.466T>G
XR_933922.1:n.466T>G
XR_933923.1:n.466T>G
NM_001363749.1:c.146T>G	NP_001350678.1:p.Leu49Arg
NM_001893.5:c.146T>G	NP_001884.2:p.Leu49Arg
NM_139062.3:c.146T>G	NP_620693.1:p.Leu49Arg
NR_110578.2:n.515T>G
XM_005256336.4:c.146T>G	XP_005256393.1:p.Leu49Arg
XR_002957961.1:n.465T>G
XR_243518.4:n.465T>G
XR_430028.4:n.465T>G
XR_933922.3:n.465T>G
XR_933923.3:n.465T>G
NM_001363749.2:c.146T>G	NP_001350678.1:p.Leu49Arg
NM_001893.6:c.146T>G MANE Select	NP_001884.2:p.Leu49Arg
NM_139062.4:c.146T>G	NP_620693.1:p.Leu49Arg