Canonical Allele Identifier: CA10603345

Gene: CACNA1A

Linked Data

• ClinVar Variation Id: 280762
• ClinVar RCV Id: RCV000317331 ; RCV000802158
• dbSNP Id: rs886041909
• MyVariant Identifiers: chr19:g.13372412A>G (hg19) ; chr19:g.13261598A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13261598A>G , CM000681.2:g.13261598A>G	GRCh38
NC_000019.9:g.13372412A>G , CM000681.1:g.13372412A>G	GRCh37
NC_000019.8:g.13233412A>G	NCBI36
NG_011569.1:g.249863T>C , LRG_7:g.249863T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360228.11:c.4102T>C MANE Select	ENSP00000353362.5:p.Cys1368Arg
ENST00000573710.7:c.4108T>C	ENSP00000460092.3:p.Cys1370Arg
ENST00000590205.2:n.1108T>C
ENST00000635727.1:c.4105T>C	ENSP00000490001.1:p.Cys1369Arg
ENST00000635742.1:n.91T>C
ENST00000635895.1:c.4105T>C	ENSP00000490323.1:p.Cys1369Arg
ENST00000635917.1:n.594T>C
ENST00000636012.1:c.4105T>C	ENSP00000490223.1:p.Cys1369Arg
ENST00000636389.1:c.4105T>C	ENSP00000489992.1:p.Cys1369Arg
ENST00000636549.1:c.4105T>C	ENSP00000490578.1:p.Cys1369Arg
ENST00000636816.1:n.790T>C
ENST00000637004.1:n.568T>C
ENST00000637276.1:c.4105T>C	ENSP00000489777.1:p.Cys1369Arg
ENST00000637432.1:c.4114T>C	ENSP00000490617.1:p.Cys1372Arg
ENST00000637692.1:n.424T>C
ENST00000637736.1:c.3964T>C	ENSP00000489861.1:p.Cys1322Arg
ENST00000637769.1:c.4105T>C	ENSP00000489778.1:p.Cys1369Arg
ENST00000637927.1:c.4108T>C	ENSP00000489715.1:p.Cys1370Arg
ENST00000638009.2:c.4105T>C	ENSP00000489913.1:p.Cys1369Arg
ENST00000638029.1:c.4114T>C	ENSP00000489829.1:p.Cys1372Arg
ENST00000664864.1:c.4300T>C	ENSP00000499449.1:p.Cys1434Arg
ENST00000360228.9:c.4102T>C	ENSP00000353362.5:p.Cys1368Arg
ENST00000573710.6:c.4105T>C	ENSP00000460092.2:p.Cys1369Arg
ENST00000585802.5:c.160T>C	ENSP00000465598.1:p.Cys54Arg
ENST00000590205.1:n.181T>C
ENST00000614285.4:c.4114T>C	ENSP00000479983.1:p.Cys1372Arg
NM_000068.3:c.4114T>C	NP_000059.3:p.Cys1372Arg
NM_001127221.1:c.4105T>C , LRG_7t1:c.4105T>C	NP_001120693.1:p.Cys1369Arg
NM_001127222.1:c.4102T>C	NP_001120694.1:p.Cys1368Arg
NM_001174080.1:c.4105T>C	NP_001167551.1:p.Cys1369Arg
NM_023035.2:c.4114T>C	NP_075461.2:p.Cys1372Arg
NM_000068.4:c.4114T>C	NP_000059.3:p.Cys1372Arg
NM_001127222.2:c.4102T>C MANE Select	NP_001120694.1:p.Cys1368Arg
NM_001174080.2:c.4105T>C	NP_001167551.1:p.Cys1369Arg
NM_023035.3:c.4114T>C	NP_075461.2:p.Cys1372Arg
NM_001127221.2:c.4105T>C	NP_001120693.1:p.Cys1369Arg