Canonical Allele Identifier: CA11947531

Gene: CSNK1A1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149509455C>T , CM000667.2:g.149509455C>T	GRCh38
NC_000005.9:g.148889018C>T , CM000667.1:g.148889018C>T	GRCh37
NC_000005.8:g.148869211C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261798.10:c.834+424G>A	ENSP00000261798.6:n.834+424G>A
ENST00000377843.8:c.750+424G>A MANE Select	ENSP00000367074.2:n.750+424G>A
ENST00000515768.6:c.834+424G>A	ENSP00000421689.2:n.834+424G>A
ENST00000606299.2:c.219+424G>A
ENST00000606719.6:c.843+424G>A	ENSP00000475319.2:n.843+424G>A
ENST00000657001.1:c.750+424G>A	ENSP00000499757.1:n.750+424G>A
ENST00000657462.1:c.*389+424G>A	ENSP00000499532.1:n.*389+424G>A
ENST00000657706.1:c.984+424G>A	ENSP00000499284.1:n.984+424G>A
ENST00000661952.1:c.*531+424G>A	ENSP00000499647.1:n.*531+424G>A
ENST00000662268.1:n.803+424G>A
ENST00000261798.9:c.750+424G>A	ENSP00000261798.5:n.750+424G>A
ENST00000377843.6:c.750+424G>A	ENSP00000367074.2:n.750+424G>A
ENST00000503350.6:c.242+424G>A
ENST00000504676.5:c.483+424G>A	ENSP00000426747.1:n.483+424G>A
ENST00000515435.5:c.567+424G>A	ENSP00000427031.1:n.567+424G>A
ENST00000515768.5:c.834+424G>A	ENSP00000421689.1:n.834+424G>A
ENST00000606299.1:c.30+424G>A	ENSP00000475633.1:n.30+424G>A
ENST00000606719.5:c.141+424G>A	ENSP00000475319.1:n.141+424G>A
ENST00000606826.5:c.205+424G>A
NM_001025105.2:c.834+424G>A	NP_001020276.1:n.834+424G>A
NM_001271741.1:c.750+424G>A	NP_001258670.1:n.750+424G>A
NM_001271742.1:c.567+424G>A	NP_001258671.1:n.567+424G>A
NM_001892.5:c.750+424G>A	NP_001883.4:n.750+424G>A
NM_001025105.3:c.834+424G>A	NP_001020276.1:n.834+424G>A
NM_001271741.2:c.750+424G>A	NP_001258670.1:n.750+424G>A
NM_001271742.2:c.567+424G>A	NP_001258671.1:n.567+424G>A
NM_001892.6:c.750+424G>A MANE Select	NP_001883.4:n.750+424G>A