Canonical Allele Identifier: CA502368400

Gene: CSNK1D

Linked Data

• MyVariant Identifiers: chr17:g.80223638G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265762G>A , CM000679.2:g.82265762G>A	GRCh38
NC_000017.10:g.80223638G>A , CM000679.1:g.80223638G>A	GRCh37
NC_000017.9:g.77816927G>A	NCBI36
NG_012828.1:g.12936C>T
NG_012828.2:g.12981C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.111C>T	ENSP00000376146.2:p.Ile37=
ENST00000314028.11:c.111C>T MANE Select	ENSP00000324464.6:p.Ile37=
ENST00000314028.10:c.111C>T	ENSP00000324464.6:p.Ile37=
ENST00000392334.6:c.111C>T	ENSP00000376146.2:p.Ile37=
ENST00000398519.9:c.111C>T	ENSP00000381531.5:p.Ile37=
ENST00000403276.7:c.111C>T	ENSP00000385769.3:p.Ile37=
ENST00000578194.5:n.317C>T
ENST00000579308.1:n.136C>T
ENST00000579316.5:n.168C>T
ENST00000580061.5:n.111C>T
ENST00000580446.1:c.76+7544C>T	ENSP00000463757.1:n.76+7544C>T
ENST00000581241.5:n.99C>T
ENST00000581660.5:c.*149C>T	ENSP00000464551.1:n.*149C>T
ENST00000582844.5:n.69C>T
ENST00000584472.5:n.196C>T
ENST00000585026.1:c.*157C>T	ENSP00000462144.1:n.*157C>T
NM_001893.4:c.111C>T	NP_001884.2:p.Ile37=
NM_139062.2:c.111C>T	NP_620693.1:p.Ile37=
NR_110578.1:n.472C>T
XM_005256336.2:c.111C>T	XP_005256393.1:p.Ile37=
XM_005256337.3:c.111C>T	XP_005256394.1:p.Ile37=
XR_243518.2:n.431C>T
XR_430028.2:n.431C>T
XR_933922.1:n.431C>T
XR_933923.1:n.431C>T
NM_001363749.1:c.111C>T	NP_001350678.1:p.Ile37=
NM_001893.5:c.111C>T	NP_001884.2:p.Ile37=
NM_139062.3:c.111C>T	NP_620693.1:p.Ile37=
NR_110578.2:n.480C>T
XM_005256336.4:c.111C>T	XP_005256393.1:p.Ile37=
XR_002957961.1:n.430C>T
XR_243518.4:n.430C>T
XR_430028.4:n.430C>T
XR_933922.3:n.430C>T
XR_933923.3:n.430C>T
NM_001363749.2:c.111C>T	NP_001350678.1:p.Ile37=
NM_001893.6:c.111C>T MANE Select	NP_001884.2:p.Ile37=
NM_139062.4:c.111C>T	NP_620693.1:p.Ile37=