Canonical Allele Identifier: CA401596975

Gene: CSNK1D

Linked Data

• MyVariant Identifiers: chr17:g.80223627C>A (hg19) ; chr17:g.82265751C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265751C>A , CM000679.2:g.82265751C>A	GRCh38
NC_000017.10:g.80223627C>A , CM000679.1:g.80223627C>A	GRCh37
NC_000017.9:g.77816916C>A	NCBI36
NG_012828.1:g.12947G>T
NG_012828.2:g.12992G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.122G>T	ENSP00000376146.2:p.Cys41Phe
ENST00000314028.11:c.122G>T MANE Select	ENSP00000324464.6:p.Cys41Phe
ENST00000314028.10:c.122G>T	ENSP00000324464.6:p.Cys41Phe
ENST00000392334.6:c.122G>T	ENSP00000376146.2:p.Cys41Phe
ENST00000398519.9:c.122G>T	ENSP00000381531.5:p.Cys41Phe
ENST00000403276.7:c.122G>T	ENSP00000385769.3:p.Cys41Phe
ENST00000578194.5:n.328G>T
ENST00000579308.1:n.147G>T
ENST00000579316.5:n.179G>T
ENST00000580061.5:n.122G>T
ENST00000580446.1:c.76+7555G>T	ENSP00000463757.1:n.76+7555G>T
ENST00000581241.5:n.110G>T
ENST00000581660.5:c.*160G>T	ENSP00000464551.1:n.*160G>T
ENST00000582844.5:n.80G>T
ENST00000584472.5:n.207G>T
ENST00000585026.1:c.*168G>T	ENSP00000462144.1:n.*168G>T
NM_001893.4:c.122G>T	NP_001884.2:p.Cys41Phe
NM_139062.2:c.122G>T	NP_620693.1:p.Cys41Phe
NR_110578.1:n.483G>T
XM_005256336.2:c.122G>T	XP_005256393.1:p.Cys41Phe
XM_005256337.3:c.122G>T	XP_005256394.1:p.Cys41Phe
XR_243518.2:n.442G>T
XR_430028.2:n.442G>T
XR_933922.1:n.442G>T
XR_933923.1:n.442G>T
NM_001363749.1:c.122G>T	NP_001350678.1:p.Cys41Phe
NM_001893.5:c.122G>T	NP_001884.2:p.Cys41Phe
NM_139062.3:c.122G>T	NP_620693.1:p.Cys41Phe
NR_110578.2:n.491G>T
XM_005256336.4:c.122G>T	XP_005256393.1:p.Cys41Phe
XR_002957961.1:n.441G>T
XR_243518.4:n.441G>T
XR_430028.4:n.441G>T
XR_933922.3:n.441G>T
XR_933923.3:n.441G>T
NM_001363749.2:c.122G>T	NP_001350678.1:p.Cys41Phe
NM_001893.6:c.122G>T MANE Select	NP_001884.2:p.Cys41Phe
NM_139062.4:c.122G>T	NP_620693.1:p.Cys41Phe