Canonical Allele Identifier: CA401596928

Gene: CSNK1D

Linked Data

• MyVariant Identifiers: chr17:g.80223615T>A (hg19) ; chr17:g.82265739T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265739T>A , CM000679.2:g.82265739T>A	GRCh38
NC_000017.10:g.80223615T>A , CM000679.1:g.80223615T>A	GRCh37
NC_000017.9:g.77816904T>A	NCBI36
NG_012828.1:g.12959A>T
NG_012828.2:g.13004A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.134A>T	ENSP00000376146.2:p.Lys45Ile
ENST00000314028.11:c.134A>T MANE Select	ENSP00000324464.6:p.Lys45Ile
ENST00000314028.10:c.134A>T	ENSP00000324464.6:p.Lys45Ile
ENST00000392334.6:c.134A>T	ENSP00000376146.2:p.Lys45Ile
ENST00000398519.9:c.134A>T	ENSP00000381531.5:p.Lys45Ile
ENST00000403276.7:c.134A>T	ENSP00000385769.3:p.Lys45Ile
ENST00000578194.5:n.340A>T
ENST00000579308.1:n.159A>T
ENST00000579316.5:n.191A>T
ENST00000580061.5:n.134A>T
ENST00000580446.1:c.76+7567A>T	ENSP00000463757.1:n.76+7567A>T
ENST00000581241.5:n.122A>T
ENST00000581660.5:c.*172A>T	ENSP00000464551.1:n.*172A>T
ENST00000582844.5:n.92A>T
ENST00000584472.5:n.219A>T
ENST00000585026.1:c.*180A>T	ENSP00000462144.1:n.*180A>T
NM_001893.4:c.134A>T	NP_001884.2:p.Lys45Ile
NM_139062.2:c.134A>T	NP_620693.1:p.Lys45Ile
NR_110578.1:n.495A>T
XM_005256336.2:c.134A>T	XP_005256393.1:p.Lys45Ile
XM_005256337.3:c.134A>T	XP_005256394.1:p.Lys45Ile
XR_243518.2:n.454A>T
XR_430028.2:n.454A>T
XR_933922.1:n.454A>T
XR_933923.1:n.454A>T
NM_001363749.1:c.134A>T	NP_001350678.1:p.Lys45Ile
NM_001893.5:c.134A>T	NP_001884.2:p.Lys45Ile
NM_139062.3:c.134A>T	NP_620693.1:p.Lys45Ile
NR_110578.2:n.503A>T
XM_005256336.4:c.134A>T	XP_005256393.1:p.Lys45Ile
XR_002957961.1:n.453A>T
XR_243518.4:n.453A>T
XR_430028.4:n.453A>T
XR_933922.3:n.453A>T
XR_933923.3:n.453A>T
NM_001363749.2:c.134A>T	NP_001350678.1:p.Lys45Ile
NM_001893.6:c.134A>T MANE Select	NP_001884.2:p.Lys45Ile
NM_139062.4:c.134A>T	NP_620693.1:p.Lys45Ile