Canonical Allele Identifier: CA1590529283

Gene: CSNK1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149524529A= , CM000667.2:g.149524529A=	GRCh38
NC_000005.9:g.148904092A= , CM000667.1:g.148904092A=	GRCh37
NC_000005.8:g.148884285A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000261798.10:c.357+516T=	ENSP00000261798.6:n.357+516T=
ENST00000377843.8:c.357+516T= MANE Select	ENSP00000367074.2:n.357+516T=
ENST00000515768.6:c.357+516T=	ENSP00000421689.2:n.357+516T=
ENST00000606719.6:c.357+516T=	ENSP00000475319.2:n.357+516T=
ENST00000657001.1:c.357+516T=	ENSP00000499757.1:n.357+516T=
ENST00000657462.1:c.231-4141T=	ENSP00000499532.1:n.231-4141T=
ENST00000657706.1:c.591+516T=	ENSP00000499284.1:n.591+516T=
ENST00000661952.1:c.231-4141T=	ENSP00000499647.1:n.231-4141T=
ENST00000662268.1:n.326+516T=
ENST00000670598.1:c.349-4141T=	ENSP00000499782.1:n.349-4141T=
ENST00000261798.9:c.357+516T=	ENSP00000261798.5:n.357+516T=
ENST00000377843.6:c.357+516T=	ENSP00000367074.2:n.357+516T=
ENST00000504676.5:c.90+516T=	ENSP00000426747.1:n.90+516T=
ENST00000515435.5:c.90+516T=	ENSP00000427031.1:n.90+516T=
ENST00000515768.5:c.357+516T=	ENSP00000421689.1:n.357+516T=
NM_001025105.2:c.357+516T=	NP_001020276.1:n.357+516T=
NM_001271741.1:c.357+516T=	NP_001258670.1:n.357+516T=
NM_001271742.1:c.90+516T=	NP_001258671.1:n.90+516T=
NM_001892.5:c.357+516T=	NP_001883.4:n.357+516T=
NM_001025105.3:c.357+516T=	NP_001020276.1:n.357+516T=
NM_001271741.2:c.357+516T=	NP_001258670.1:n.357+516T=
NM_001271742.2:c.90+516T=	NP_001258671.1:n.90+516T=
NM_001892.6:c.357+516T= MANE Select	NP_001883.4:n.357+516T=