Canonical Allele Identifier: CA502368362

Gene: CSNK1D

Linked Data

• COSMIC: COSM1303538 ; COSM1303539
• MyVariant Identifiers: chr17:g.80223620T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265744T>C , CM000679.2:g.82265744T>C	GRCh38
NC_000017.10:g.80223620T>C , CM000679.1:g.80223620T>C	GRCh37
NC_000017.9:g.77816909T>C	NCBI36
NG_012828.1:g.12954A>G
NG_012828.2:g.12999A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.129A>G	ENSP00000376146.2:p.Lys43=
ENST00000314028.11:c.129A>G MANE Select	ENSP00000324464.6:p.Lys43=
ENST00000314028.10:c.129A>G	ENSP00000324464.6:p.Lys43=
ENST00000392334.6:c.129A>G	ENSP00000376146.2:p.Lys43=
ENST00000398519.9:c.129A>G	ENSP00000381531.5:p.Lys43=
ENST00000403276.7:c.129A>G	ENSP00000385769.3:p.Lys43=
ENST00000578194.5:n.335A>G
ENST00000579308.1:n.154A>G
ENST00000579316.5:n.186A>G
ENST00000580061.5:n.129A>G
ENST00000580446.1:c.76+7562A>G	ENSP00000463757.1:n.76+7562A>G
ENST00000581241.5:n.117A>G
ENST00000581660.5:c.*167A>G	ENSP00000464551.1:n.*167A>G
ENST00000582844.5:n.87A>G
ENST00000584472.5:n.214A>G
ENST00000585026.1:c.*175A>G	ENSP00000462144.1:n.*175A>G
NM_001893.4:c.129A>G	NP_001884.2:p.Lys43=
NM_139062.2:c.129A>G	NP_620693.1:p.Lys43=
NR_110578.1:n.490A>G
XM_005256336.2:c.129A>G	XP_005256393.1:p.Lys43=
XM_005256337.3:c.129A>G	XP_005256394.1:p.Lys43=
XR_243518.2:n.449A>G
XR_430028.2:n.449A>G
XR_933922.1:n.449A>G
XR_933923.1:n.449A>G
NM_001363749.1:c.129A>G	NP_001350678.1:p.Lys43=
NM_001893.5:c.129A>G	NP_001884.2:p.Lys43=
NM_139062.3:c.129A>G	NP_620693.1:p.Lys43=
NR_110578.2:n.498A>G
XM_005256336.4:c.129A>G	XP_005256393.1:p.Lys43=
XR_002957961.1:n.448A>G
XR_243518.4:n.448A>G
XR_430028.4:n.448A>G
XR_933922.3:n.448A>G
XR_933923.3:n.448A>G
NM_001363749.2:c.129A>G	NP_001350678.1:p.Lys43=
NM_001893.6:c.129A>G MANE Select	NP_001884.2:p.Lys43=
NM_139062.4:c.129A>G	NP_620693.1:p.Lys43=