Canonical Allele Identifier: CA401597038

Gene: CSNK1D

Linked Data

• MyVariant Identifiers: chr17:g.80223642G>T (hg19) ; chr17:g.82265766G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265766G>T , CM000679.2:g.82265766G>T	GRCh38
NC_000017.10:g.80223642G>T , CM000679.1:g.80223642G>T	GRCh37
NC_000017.9:g.77816931G>T	NCBI36
NG_012828.1:g.12932C>A
NG_012828.2:g.12977C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.107C>A	ENSP00000376146.2:p.Ala36Asp
ENST00000314028.11:c.107C>A MANE Select	ENSP00000324464.6:p.Ala36Asp
ENST00000314028.10:c.107C>A	ENSP00000324464.6:p.Ala36Asp
ENST00000392334.6:c.107C>A	ENSP00000376146.2:p.Ala36Asp
ENST00000398519.9:c.107C>A	ENSP00000381531.5:p.Ala36Asp
ENST00000403276.7:c.107C>A	ENSP00000385769.3:p.Ala36Asp
ENST00000578194.5:n.313C>A
ENST00000579308.1:n.132C>A
ENST00000579316.5:n.164C>A
ENST00000580061.5:n.107C>A
ENST00000580446.1:c.76+7540C>A	ENSP00000463757.1:n.76+7540C>A
ENST00000581241.5:n.95C>A
ENST00000581660.5:c.*145C>A	ENSP00000464551.1:n.*145C>A
ENST00000582844.5:n.65C>A
ENST00000584472.5:n.192C>A
ENST00000585026.1:c.*153C>A	ENSP00000462144.1:n.*153C>A
NM_001893.4:c.107C>A	NP_001884.2:p.Ala36Asp
NM_139062.2:c.107C>A	NP_620693.1:p.Ala36Asp
NR_110578.1:n.468C>A
XM_005256336.2:c.107C>A	XP_005256393.1:p.Ala36Asp
XM_005256337.3:c.107C>A	XP_005256394.1:p.Ala36Asp
XR_243518.2:n.427C>A
XR_430028.2:n.427C>A
XR_933922.1:n.427C>A
XR_933923.1:n.427C>A
NM_001363749.1:c.107C>A	NP_001350678.1:p.Ala36Asp
NM_001893.5:c.107C>A	NP_001884.2:p.Ala36Asp
NM_139062.3:c.107C>A	NP_620693.1:p.Ala36Asp
NR_110578.2:n.476C>A
XM_005256336.4:c.107C>A	XP_005256393.1:p.Ala36Asp
XR_002957961.1:n.426C>A
XR_243518.4:n.426C>A
XR_430028.4:n.426C>A
XR_933922.3:n.426C>A
XR_933923.3:n.426C>A
NM_001363749.2:c.107C>A	NP_001350678.1:p.Ala36Asp
NM_001893.6:c.107C>A MANE Select	NP_001884.2:p.Ala36Asp
NM_139062.4:c.107C>A	NP_620693.1:p.Ala36Asp