Canonical Allele Identifier: CA2278930056

Gene: CSNK1D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82265792C= , CM000679.2:g.82265792C=	GRCh38
NC_000017.10:g.80223668C= , CM000679.1:g.80223668C=	GRCh37
NC_000017.9:g.77816957C=	NCBI36
NG_012828.1:g.12906G=
NG_012828.2:g.12951G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392334.7:c.81G=	ENSP00000376146.2:p.Thr27=
ENST00000314028.11:c.81G= MANE Select	ENSP00000324464.6:p.Thr27=
ENST00000314028.10:c.81G=	ENSP00000324464.6:p.Thr27=
ENST00000392334.6:c.81G=	ENSP00000376146.2:p.Thr27=
ENST00000398519.9:c.81G=	ENSP00000381531.5:p.Thr27=
ENST00000403276.7:c.81G=	ENSP00000385769.3:p.Thr27=
ENST00000578194.5:n.287G=
ENST00000579308.1:n.106G=
ENST00000579316.5:n.138G=
ENST00000580061.5:n.81G=
ENST00000580446.1:c.76+7514G=	ENSP00000463757.1:n.76+7514G=
ENST00000581241.5:n.69G=
ENST00000581660.5:c.*119G=	ENSP00000464551.1:n.*119G=
ENST00000582844.5:n.39G=
ENST00000584472.5:n.166G=
ENST00000585026.1:c.*127G=	ENSP00000462144.1:n.*127G=
NM_001893.4:c.81G=	NP_001884.2:p.Thr27=
NM_139062.2:c.81G=	NP_620693.1:p.Thr27=
NR_110578.1:n.442G=
XM_005256336.2:c.81G=	XP_005256393.1:p.Thr27=
XM_005256337.3:c.81G=	XP_005256394.1:p.Thr27=
XR_243518.2:n.401G=
XR_430028.2:n.401G=
XR_933922.1:n.401G=
XR_933923.1:n.401G=
NM_001363749.1:c.81G=	NP_001350678.1:p.Thr27=
NM_001893.5:c.81G=	NP_001884.2:p.Thr27=
NM_139062.3:c.81G=	NP_620693.1:p.Thr27=
NR_110578.2:n.450G=
XM_005256336.4:c.81G=	XP_005256393.1:p.Thr27=
XR_002957961.1:n.400G=
XR_243518.4:n.400G=
XR_430028.4:n.400G=
XR_933922.3:n.400G=
XR_933923.3:n.400G=
NM_001363749.2:c.81G=	NP_001350678.1:p.Thr27=
NM_001893.6:c.81G= MANE Select	NP_001884.2:p.Thr27=
NM_139062.4:c.81G=	NP_620693.1:p.Thr27=