Canonical Allele Identifier: CA401596708

Gene: CSNK1D

Linked Data

• MyVariant Identifiers: chr17:g.80223564C>A (hg19) ; chr17:g.82265688C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265688C>A , CM000679.2:g.82265688C>A	GRCh38
NC_000017.10:g.80223564C>A , CM000679.1:g.80223564C>A	GRCh37
NC_000017.9:g.77816853C>A	NCBI36
NG_012828.1:g.13010G>T
NG_012828.2:g.13055G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.185G>T	ENSP00000376146.2:p.Gly62Val
ENST00000314028.11:c.185G>T MANE Select	ENSP00000324464.6:p.Gly62Val
ENST00000314028.10:c.185G>T	ENSP00000324464.6:p.Gly62Val
ENST00000392334.6:c.185G>T	ENSP00000376146.2:p.Gly62Val
ENST00000398519.9:c.185G>T	ENSP00000381531.5:p.Gly62Val
ENST00000403276.7:c.185G>T	ENSP00000385769.3:p.Gly62Val
ENST00000578194.5:n.391G>T
ENST00000579308.1:n.210G>T
ENST00000579316.5:n.242G>T
ENST00000580061.5:n.185G>T
ENST00000580446.1:c.76+7618G>T	ENSP00000463757.1:n.76+7618G>T
ENST00000581241.5:n.173G>T
ENST00000581660.5:c.*223G>T	ENSP00000464551.1:n.*223G>T
ENST00000582844.5:n.143G>T
ENST00000584472.5:n.270G>T
ENST00000585026.1:c.*231G>T	ENSP00000462144.1:n.*231G>T
NM_001893.4:c.185G>T	NP_001884.2:p.Gly62Val
NM_139062.2:c.185G>T	NP_620693.1:p.Gly62Val
NR_110578.1:n.546G>T
XM_005256336.2:c.185G>T	XP_005256393.1:p.Gly62Val
XM_005256337.3:c.185G>T	XP_005256394.1:p.Gly62Val
XR_243518.2:n.505G>T
XR_430028.2:n.505G>T
XR_933922.1:n.505G>T
XR_933923.1:n.505G>T
NM_001363749.1:c.185G>T	NP_001350678.1:p.Gly62Val
NM_001893.5:c.185G>T	NP_001884.2:p.Gly62Val
NM_139062.3:c.185G>T	NP_620693.1:p.Gly62Val
NR_110578.2:n.554G>T
XM_005256336.4:c.185G>T	XP_005256393.1:p.Gly62Val
XR_002957961.1:n.504G>T
XR_243518.4:n.504G>T
XR_430028.4:n.504G>T
XR_933922.3:n.504G>T
XR_933923.3:n.504G>T
NM_001363749.2:c.185G>T	NP_001350678.1:p.Gly62Val
NM_001893.6:c.185G>T MANE Select	NP_001884.2:p.Gly62Val
NM_139062.4:c.185G>T	NP_620693.1:p.Gly62Val