Canonical Allele Identifier: CA502368455

Gene: CSNK1D

Linked Data

• MyVariant Identifiers: chr17:g.80223653T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265777T>G , CM000679.2:g.82265777T>G	GRCh38
NC_000017.10:g.80223653T>G , CM000679.1:g.80223653T>G	GRCh37
NC_000017.9:g.77816942T>G	NCBI36
NG_012828.1:g.12921A>C
NG_012828.2:g.12966A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.96A>C	ENSP00000376146.2:p.Gly32=
ENST00000314028.11:c.96A>C MANE Select	ENSP00000324464.6:p.Gly32=
ENST00000314028.10:c.96A>C	ENSP00000324464.6:p.Gly32=
ENST00000392334.6:c.96A>C	ENSP00000376146.2:p.Gly32=
ENST00000398519.9:c.96A>C	ENSP00000381531.5:p.Gly32=
ENST00000403276.7:c.96A>C	ENSP00000385769.3:p.Gly32=
ENST00000578194.5:n.302A>C
ENST00000579308.1:n.121A>C
ENST00000579316.5:n.153A>C
ENST00000580061.5:n.96A>C
ENST00000580446.1:c.76+7529A>C	ENSP00000463757.1:n.76+7529A>C
ENST00000581241.5:n.84A>C
ENST00000581660.5:c.*134A>C	ENSP00000464551.1:n.*134A>C
ENST00000582844.5:n.54A>C
ENST00000584472.5:n.181A>C
ENST00000585026.1:c.*142A>C	ENSP00000462144.1:n.*142A>C
NM_001893.4:c.96A>C	NP_001884.2:p.Gly32=
NM_139062.2:c.96A>C	NP_620693.1:p.Gly32=
NR_110578.1:n.457A>C
XM_005256336.2:c.96A>C	XP_005256393.1:p.Gly32=
XM_005256337.3:c.96A>C	XP_005256394.1:p.Gly32=
XR_243518.2:n.416A>C
XR_430028.2:n.416A>C
XR_933922.1:n.416A>C
XR_933923.1:n.416A>C
NM_001363749.1:c.96A>C	NP_001350678.1:p.Gly32=
NM_001893.5:c.96A>C	NP_001884.2:p.Gly32=
NM_139062.3:c.96A>C	NP_620693.1:p.Gly32=
NR_110578.2:n.465A>C
XM_005256336.4:c.96A>C	XP_005256393.1:p.Gly32=
XR_002957961.1:n.415A>C
XR_243518.4:n.415A>C
XR_430028.4:n.415A>C
XR_933922.3:n.415A>C
XR_933923.3:n.415A>C
NM_001363749.2:c.96A>C	NP_001350678.1:p.Gly32=
NM_001893.6:c.96A>C MANE Select	NP_001884.2:p.Gly32=
NM_139062.4:c.96A>C	NP_620693.1:p.Gly32=