Canonical Allele Identifier: CA401596862

Gene: CSNK1D

Linked Data

• gnomAD v4: 17-82265723-G-C
• MyVariant Identifiers: chr17:g.80223599G>C (hg19) ; chr17:g.82265723G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265723G>C , CM000679.2:g.82265723G>C	GRCh38
NC_000017.10:g.80223599G>C , CM000679.1:g.80223599G>C	GRCh37
NC_000017.9:g.77816888G>C	NCBI36
NG_012828.1:g.12975C>G
NG_012828.2:g.13020C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.150C>G	ENSP00000376146.2:p.His50Gln
ENST00000314028.11:c.150C>G MANE Select	ENSP00000324464.6:p.His50Gln
ENST00000314028.10:c.150C>G	ENSP00000324464.6:p.His50Gln
ENST00000392334.6:c.150C>G	ENSP00000376146.2:p.His50Gln
ENST00000398519.9:c.150C>G	ENSP00000381531.5:p.His50Gln
ENST00000403276.7:c.150C>G	ENSP00000385769.3:p.His50Gln
ENST00000578194.5:n.356C>G
ENST00000579308.1:n.175C>G
ENST00000579316.5:n.207C>G
ENST00000580061.5:n.150C>G
ENST00000580446.1:c.76+7583C>G	ENSP00000463757.1:n.76+7583C>G
ENST00000581241.5:n.138C>G
ENST00000581660.5:c.*188C>G	ENSP00000464551.1:n.*188C>G
ENST00000582844.5:n.108C>G
ENST00000584472.5:n.235C>G
ENST00000585026.1:c.*196C>G	ENSP00000462144.1:n.*196C>G
NM_001893.4:c.150C>G	NP_001884.2:p.His50Gln
NM_139062.2:c.150C>G	NP_620693.1:p.His50Gln
NR_110578.1:n.511C>G
XM_005256336.2:c.150C>G	XP_005256393.1:p.His50Gln
XM_005256337.3:c.150C>G	XP_005256394.1:p.His50Gln
XR_243518.2:n.470C>G
XR_430028.2:n.470C>G
XR_933922.1:n.470C>G
XR_933923.1:n.470C>G
NM_001363749.1:c.150C>G	NP_001350678.1:p.His50Gln
NM_001893.5:c.150C>G	NP_001884.2:p.His50Gln
NM_139062.3:c.150C>G	NP_620693.1:p.His50Gln
NR_110578.2:n.519C>G
XM_005256336.4:c.150C>G	XP_005256393.1:p.His50Gln
XR_002957961.1:n.469C>G
XR_243518.4:n.469C>G
XR_430028.4:n.469C>G
XR_933922.3:n.469C>G
XR_933923.3:n.469C>G
NM_001363749.2:c.150C>G	NP_001350678.1:p.His50Gln
NM_001893.6:c.150C>G MANE Select	NP_001884.2:p.His50Gln
NM_139062.4:c.150C>G	NP_620693.1:p.His50Gln