Canonical Allele Identifier: CA2640620203

Gene: CSNK1D

Linked Data

• gnomAD v4: 17-82265590-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265590A>G , CM000679.2:g.82265590A>G	GRCh38
NC_000017.10:g.80223466A>G , CM000679.1:g.80223466A>G	GRCh37
NC_000017.9:g.77816755A>G	NCBI36
NG_012828.1:g.13108T>C
NG_012828.2:g.13153T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.187+96T>C	ENSP00000376146.2:n.187+96T>C
ENST00000314028.11:c.187+96T>C MANE Select	ENSP00000324464.6:n.187+96T>C
ENST00000314028.10:c.187+96T>C	ENSP00000324464.6:n.187+96T>C
ENST00000392334.6:c.187+96T>C	ENSP00000376146.2:n.187+96T>C
ENST00000398519.9:c.187+96T>C	ENSP00000381531.5:n.187+96T>C
ENST00000403276.7:c.187+96T>C	ENSP00000385769.3:n.187+96T>C
ENST00000578194.5:n.393+96T>C
ENST00000579308.1:n.308T>C
ENST00000579316.5:n.244+96T>C
ENST00000580061.5:n.187+96T>C
ENST00000580446.1:c.76+7716T>C	ENSP00000463757.1:n.76+7716T>C
ENST00000581241.5:n.175+96T>C
ENST00000581660.5:c.*225+96T>C	ENSP00000464551.1:n.*225+96T>C
ENST00000582844.5:n.145+96T>C
ENST00000584472.5:n.272+96T>C
ENST00000585026.1:c.*233+96T>C	ENSP00000462144.1:n.*233+96T>C
NM_001893.4:c.187+96T>C	NP_001884.2:n.187+96T>C
NM_139062.2:c.187+96T>C	NP_620693.1:n.187+96T>C
NR_110578.1:n.548+96T>C
XM_005256336.2:c.187+96T>C	XP_005256393.1:n.187+96T>C
XM_005256337.3:c.187+96T>C	XP_005256394.1:n.187+96T>C
XR_243518.2:n.507+96T>C
XR_430028.2:n.507+96T>C
XR_933922.1:n.507+96T>C
XR_933923.1:n.507+96T>C
NM_001363749.1:c.187+96T>C	NP_001350678.1:n.187+96T>C
NM_001893.5:c.187+96T>C	NP_001884.2:n.187+96T>C
NM_139062.3:c.187+96T>C	NP_620693.1:n.187+96T>C
NR_110578.2:n.556+96T>C
XM_005256336.4:c.187+96T>C	XP_005256393.1:n.187+96T>C
XR_002957961.1:n.506+96T>C
XR_243518.4:n.506+96T>C
XR_430028.4:n.506+96T>C
XR_933922.3:n.506+96T>C
XR_933923.3:n.506+96T>C
NM_001363749.2:c.187+96T>C	NP_001350678.1:n.187+96T>C
NM_001893.6:c.187+96T>C MANE Select	NP_001884.2:n.187+96T>C
NM_139062.4:c.187+96T>C	NP_620693.1:n.187+96T>C