Canonical Allele Identifier: CA401597106

Gene: CSNK1D

Linked Data

• MyVariant Identifiers: chr17:g.80223650T>G (hg19) ; chr17:g.82265774T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265774T>G , CM000679.2:g.82265774T>G	GRCh38
NC_000017.10:g.80223650T>G , CM000679.1:g.80223650T>G	GRCh37
NC_000017.9:g.77816939T>G	NCBI36
NG_012828.1:g.12924A>C
NG_012828.2:g.12969A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.99A>C	ENSP00000376146.2:p.Glu33Asp
ENST00000314028.11:c.99A>C MANE Select	ENSP00000324464.6:p.Glu33Asp
ENST00000314028.10:c.99A>C	ENSP00000324464.6:p.Glu33Asp
ENST00000392334.6:c.99A>C	ENSP00000376146.2:p.Glu33Asp
ENST00000398519.9:c.99A>C	ENSP00000381531.5:p.Glu33Asp
ENST00000403276.7:c.99A>C	ENSP00000385769.3:p.Glu33Asp
ENST00000578194.5:n.305A>C
ENST00000579308.1:n.124A>C
ENST00000579316.5:n.156A>C
ENST00000580061.5:n.99A>C
ENST00000580446.1:c.76+7532A>C	ENSP00000463757.1:n.76+7532A>C
ENST00000581241.5:n.87A>C
ENST00000581660.5:c.*137A>C	ENSP00000464551.1:n.*137A>C
ENST00000582844.5:n.57A>C
ENST00000584472.5:n.184A>C
ENST00000585026.1:c.*145A>C	ENSP00000462144.1:n.*145A>C
NM_001893.4:c.99A>C	NP_001884.2:p.Glu33Asp
NM_139062.2:c.99A>C	NP_620693.1:p.Glu33Asp
NR_110578.1:n.460A>C
XM_005256336.2:c.99A>C	XP_005256393.1:p.Glu33Asp
XM_005256337.3:c.99A>C	XP_005256394.1:p.Glu33Asp
XR_243518.2:n.419A>C
XR_430028.2:n.419A>C
XR_933922.1:n.419A>C
XR_933923.1:n.419A>C
NM_001363749.1:c.99A>C	NP_001350678.1:p.Glu33Asp
NM_001893.5:c.99A>C	NP_001884.2:p.Glu33Asp
NM_139062.3:c.99A>C	NP_620693.1:p.Glu33Asp
NR_110578.2:n.468A>C
XM_005256336.4:c.99A>C	XP_005256393.1:p.Glu33Asp
XR_002957961.1:n.418A>C
XR_243518.4:n.418A>C
XR_430028.4:n.418A>C
XR_933922.3:n.418A>C
XR_933923.3:n.418A>C
NM_001363749.2:c.99A>C	NP_001350678.1:p.Glu33Asp
NM_001893.6:c.99A>C MANE Select	NP_001884.2:p.Glu33Asp
NM_139062.4:c.99A>C	NP_620693.1:p.Glu33Asp