Canonical Allele Identifier: CA9239626
Gene: CACNA1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13224748C>T , CM000681.2:g.13224748C>T GRCh38
NC_000019.9:g.13335562C>T , CM000681.1:g.13335562C>T GRCh37
NC_000019.8:g.13196562C>T NCBI36
NG_011569.1:g.286713G>A , LRG_7:g.286713G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360228.11:c.5650G>A MANE Select ENSP00000353362.5:p.Val1884Ile
ENST00000573710.7:c.5656G>A ENSP00000460092.3:p.Val1886Ile
ENST00000585802.6:c.811G>A ENSP00000465598.2:p.Val271Ile
ENST00000635727.1:c.5653G>A ENSP00000490001.1:p.Val1885Ile
ENST00000635895.1:c.5653G>A ENSP00000490323.1:p.Val1885Ile
ENST00000635988.1:n.1808G>A
ENST00000636012.1:c.5653G>A ENSP00000490223.1:p.Val1885Ile
ENST00000636389.1:c.5653G>A ENSP00000489992.1:p.Val1885Ile
ENST00000636473.1:c.520G>A ENSP00000490173.1:p.Val174Ile
ENST00000636549.1:c.5659G>A ENSP00000490578.1:p.Val1887Ile
ENST00000636610.1:n.567G>A
ENST00000636768.1:c.180G>A ENSP00000490190.1:p.Pro60=
ENST00000637276.1:c.5653G>A ENSP00000489777.1:p.Val1885Ile
ENST00000637432.1:c.5668G>A ENSP00000490617.1:p.Val1890Ile
ENST00000637736.1:c.5512G>A ENSP00000489861.1:p.Val1838Ile
ENST00000637769.1:c.5653G>A ENSP00000489778.1:p.Val1885Ile
ENST00000637819.1:c.1054G>A ENSP00000490686.1:p.Val352Ile
ENST00000637927.1:c.5656G>A ENSP00000489715.1:p.Val1886Ile
ENST00000638009.2:c.5653G>A ENSP00000489913.1:p.Val1885Ile
ENST00000638029.1:c.5668G>A ENSP00000489829.1:p.Val1890Ile
ENST00000664864.1:c.5854G>A ENSP00000499449.1:p.Val1952Ile
ENST00000360228.9:c.5650G>A ENSP00000353362.5:p.Val1884Ile
ENST00000573710.6:c.5653G>A ENSP00000460092.2:p.Val1885Ile
ENST00000585802.5:c.1708G>A ENSP00000465598.1:p.Val570Ile
ENST00000586190.1:n.209G>A
ENST00000587525.5:c.1111G>A ENSP00000467729.1:p.Val371Ile
ENST00000614285.4:c.5668G>A ENSP00000479983.1:p.Val1890Ile
NM_000068.3:c.5668G>A NP_000059.3:p.Val1890Ile
NM_001127221.1:c.5653G>A , LRG_7t1:c.5653G>A NP_001120693.1:p.Val1885Ile
NM_001127222.1:c.5650G>A NP_001120694.1:p.Val1884Ile
NM_001174080.1:c.5659G>A NP_001167551.1:p.Val1887Ile
NM_023035.2:c.5668G>A NP_075461.2:p.Val1890Ile
NM_000068.4:c.5668G>A NP_000059.3:p.Val1890Ile
NM_001127222.2:c.5650G>A MANE Select NP_001120694.1:p.Val1884Ile
NM_001174080.2:c.5659G>A NP_001167551.1:p.Val1887Ile
NM_023035.3:c.5668G>A NP_075461.2:p.Val1890Ile
NM_001127221.2:c.5653G>A NP_001120693.1:p.Val1885Ile