Canonical Allele Identifier: CA254479
Gene: CACNA1A HGNC NCBI

Linked Data

ClinVar Variation Id: 8507
ClinVar RCV Id: RCV000009032 RCV000622947 RCV000763032 RCV002466397 RCV002512927
dbSNP Id: rs121909324
MyVariant Identifiers: chr19:g.13366031G>A (hg19) chr19:g.13255217G>A (hg38)
PubMed: PMID:1564484 PMID:3358708 PMID:8898206 PMID:8988170 PMID:9005860 PMID:9302278 PMID:9403487 PMID:9436730 PMID:9559993 PMID:9879686 PMID:10408533 PMID:11179022 PMID:11564488 PMID:11723274 PMID:12707077 PMID:14718690 PMID:15300451 PMID:15483044 PMID:15710862 PMID:16043807 PMID:16325861 PMID:16595610 PMID:17142831 PMID:17495624 PMID:17575281 PMID:18498393 PMID:18541804 PMID:18940563 PMID:19484318 PMID:19811514 PMID:20097664 PMID:20129625 PMID:20156848 PMID:20204399 PMID:20233618 PMID:20682717 PMID:22249839 PMID:23441182 PMID:23771276 PMID:23831250 PMID:23934111 PMID:25735478 PMID:25758715 PMID:26814174 PMID:27476654 PMID:28742085
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13255217G>A , CM000681.2:g.13255217G>A GRCh38
NC_000019.9:g.13366031G>A , CM000681.1:g.13366031G>A GRCh37
NC_000019.8:g.13227031G>A NCBI36
NG_011569.1:g.256244C>T , LRG_7:g.256244C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360228.11:c.4633C>T MANE Select ENSP00000353362.5:p.Arg1545Ter
ENST00000573710.7:c.4639C>T ENSP00000460092.3:p.Arg1547Ter
ENST00000635727.1:c.4636C>T ENSP00000490001.1:p.Arg1546Ter
ENST00000635742.1:n.622C>T
ENST00000635895.1:c.4636C>T ENSP00000490323.1:p.Arg1546Ter
ENST00000635917.1:n.1125C>T
ENST00000636012.1:c.4636C>T ENSP00000490223.1:p.Arg1546Ter
ENST00000636389.1:c.4636C>T ENSP00000489992.1:p.Arg1546Ter
ENST00000636549.1:c.4636C>T ENSP00000490578.1:p.Arg1546Ter
ENST00000636816.1:n.1321C>T
ENST00000637004.1:n.1099C>T
ENST00000637276.1:c.4636C>T ENSP00000489777.1:p.Arg1546Ter
ENST00000637297.1:c.246+2133C>T ENSP00000489692.1:n.246+2133C>T
ENST00000637432.1:c.4645C>T ENSP00000490617.1:p.Arg1549Ter
ENST00000637692.1:n.955C>T
ENST00000637736.1:c.4495C>T ENSP00000489861.1:p.Arg1499Ter
ENST00000637769.1:c.4636C>T ENSP00000489778.1:p.Arg1546Ter
ENST00000637819.1:c.31C>T ENSP00000490686.1:p.Arg11Ter
ENST00000637927.1:c.4639C>T ENSP00000489715.1:p.Arg1547Ter
ENST00000638009.2:c.4636C>T ENSP00000489913.1:p.Arg1546Ter
ENST00000638029.1:c.4645C>T ENSP00000489829.1:p.Arg1549Ter
ENST00000664864.1:c.4831C>T ENSP00000499449.1:p.Arg1611Ter
ENST00000360228.9:c.4633C>T ENSP00000353362.5:p.Arg1545Ter
ENST00000573710.6:c.4636C>T ENSP00000460092.2:p.Arg1546Ter
ENST00000585802.5:c.691C>T ENSP00000465598.1:p.Arg231Ter
ENST00000587525.5:c.94C>T ENSP00000467729.1:p.Arg32Ter
ENST00000614285.4:c.4645C>T ENSP00000479983.1:p.Arg1549Ter
NM_000068.3:c.4645C>T NP_000059.3:p.Arg1549Ter
NM_001127221.1:c.4636C>T , LRG_7t1:c.4636C>T NP_001120693.1:p.Arg1546Ter
NM_001127222.1:c.4633C>T NP_001120694.1:p.Arg1545Ter
NM_001174080.1:c.4636C>T NP_001167551.1:p.Arg1546Ter
NM_023035.2:c.4645C>T NP_075461.2:p.Arg1549Ter
NM_000068.4:c.4645C>T NP_000059.3:p.Arg1549Ter
NM_001127222.2:c.4633C>T MANE Select NP_001120694.1:p.Arg1545Ter
NM_001174080.2:c.4636C>T NP_001167551.1:p.Arg1546Ter
NM_023035.3:c.4645C>T NP_075461.2:p.Arg1549Ter
NM_001127221.2:c.4636C>T NP_001120693.1:p.Arg1546Ter
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Search 100 bp 3'