Canonical Allele Identifier: CA401597025

Gene: CSNK1D

Linked Data

• MyVariant Identifiers: chr17:g.80223639A>C (hg19) ; chr17:g.82265763A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265763A>C , CM000679.2:g.82265763A>C	GRCh38
NC_000017.10:g.80223639A>C , CM000679.1:g.80223639A>C	GRCh37
NC_000017.9:g.77816928A>C	NCBI36
NG_012828.1:g.12935T>G
NG_012828.2:g.12980T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.110T>G	ENSP00000376146.2:p.Ile37Ser
ENST00000314028.11:c.110T>G MANE Select	ENSP00000324464.6:p.Ile37Ser
ENST00000314028.10:c.110T>G	ENSP00000324464.6:p.Ile37Ser
ENST00000392334.6:c.110T>G	ENSP00000376146.2:p.Ile37Ser
ENST00000398519.9:c.110T>G	ENSP00000381531.5:p.Ile37Ser
ENST00000403276.7:c.110T>G	ENSP00000385769.3:p.Ile37Ser
ENST00000578194.5:n.316T>G
ENST00000579308.1:n.135T>G
ENST00000579316.5:n.167T>G
ENST00000580061.5:n.110T>G
ENST00000580446.1:c.76+7543T>G	ENSP00000463757.1:n.76+7543T>G
ENST00000581241.5:n.98T>G
ENST00000581660.5:c.*148T>G	ENSP00000464551.1:n.*148T>G
ENST00000582844.5:n.68T>G
ENST00000584472.5:n.195T>G
ENST00000585026.1:c.*156T>G	ENSP00000462144.1:n.*156T>G
NM_001893.4:c.110T>G	NP_001884.2:p.Ile37Ser
NM_139062.2:c.110T>G	NP_620693.1:p.Ile37Ser
NR_110578.1:n.471T>G
XM_005256336.2:c.110T>G	XP_005256393.1:p.Ile37Ser
XM_005256337.3:c.110T>G	XP_005256394.1:p.Ile37Ser
XR_243518.2:n.430T>G
XR_430028.2:n.430T>G
XR_933922.1:n.430T>G
XR_933923.1:n.430T>G
NM_001363749.1:c.110T>G	NP_001350678.1:p.Ile37Ser
NM_001893.5:c.110T>G	NP_001884.2:p.Ile37Ser
NM_139062.3:c.110T>G	NP_620693.1:p.Ile37Ser
NR_110578.2:n.479T>G
XM_005256336.4:c.110T>G	XP_005256393.1:p.Ile37Ser
XR_002957961.1:n.429T>G
XR_243518.4:n.429T>G
XR_430028.4:n.429T>G
XR_933922.3:n.429T>G
XR_933923.3:n.429T>G
NM_001363749.2:c.110T>G	NP_001350678.1:p.Ile37Ser
NM_001893.6:c.110T>G MANE Select	NP_001884.2:p.Ile37Ser
NM_139062.4:c.110T>G	NP_620693.1:p.Ile37Ser