Canonical Allele Identifier: CA658795584

Gene: CACNA1S

Linked Data

• ClinVar Variation Id: 509777
• ClinVar RCV Id: RCV000613168 ; RCV001860279
• dbSNP Id: rs1454687459
• gnomAD v3: 1-201089249-C-T
• gnomAD v4: 1-201089249-C-T
• MyVariant Identifiers: chr1:g.201058377C>T (hg19) ; chr1:g.201089249C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201089249C>T , CM000663.2:g.201089249C>T	GRCh38
NC_000001.10:g.201058377C>T , CM000663.1:g.201058377C>T	GRCh37
NC_000001.9:g.199325000C>T	NCBI36
NG_009816.1:g.28318G>A
NG_009816.2:g.28318G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362061.4:c.900+9G>A MANE Select	ENSP00000355192.3:n.900+9G>A
ENST00000679417.1:c.909G>A	ENSP00000506706.1:p.Leu303=
ENST00000680059.1:c.900+9G>A	ENSP00000504944.1:n.900+9G>A
ENST00000681078.1:c.900+9G>A	ENSP00000506645.1:n.900+9G>A
ENST00000681190.1:c.900+9G>A	ENSP00000506428.1:n.900+9G>A
ENST00000681874.1:c.900+9G>A	ENSP00000505162.1:n.900+9G>A
ENST00000362061.3:c.900+9G>A	ENSP00000355192.3:n.900+9G>A
ENST00000367338.7:c.900+9G>A	ENSP00000356307.3:n.900+9G>A
NM_000069.2:c.900+9G>A	NP_000060.2:n.900+9G>A
XM_005245478.2:c.900+9G>A	XP_005245535.1:n.900+9G>A
XM_005245478.3:c.900+9G>A	XP_005245535.1:n.900+9G>A
NM_000069.3:c.900+9G>A MANE Select	NP_000060.2:n.900+9G>A