Canonical Allele Identifier: CA2323795495
Gene: CACNA1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13235018T= , CM000681.2:g.13235018T= GRCh38
NC_000019.9:g.13345832T= , CM000681.1:g.13345832T= GRCh37
NC_000019.8:g.13206832T= NCBI36
NG_011569.1:g.276443A= , LRG_7:g.276443A=

Transcript Alleles

HGVS Amino-acid change
ENST00000360228.11:c.5152A= MANE Select ENSP00000353362.5:p.Ile1718=
ENST00000573710.7:c.5158A= ENSP00000460092.3:p.Ile1720=
ENST00000573891.6:c.571A=
ENST00000574822.6:n.376A=
ENST00000585802.6:c.313A= ENSP00000465598.2:p.Ile105=
ENST00000593267.2:n.357A=
ENST00000635727.1:c.5155A= ENSP00000490001.1:p.Ile1719=
ENST00000635742.1:n.1141A=
ENST00000635895.1:c.5155A= ENSP00000490323.1:p.Ile1719=
ENST00000636012.1:c.5155A= ENSP00000490223.1:p.Ile1719=
ENST00000636058.1:c.467A=
ENST00000636389.1:c.5155A= ENSP00000489992.1:p.Ile1719=
ENST00000636473.1:c.247A= ENSP00000490173.1:p.Ile83=
ENST00000636549.1:c.5161A= ENSP00000490578.1:p.Ile1721=
ENST00000637276.1:c.5155A= ENSP00000489777.1:p.Ile1719=
ENST00000637297.1:c.448A= ENSP00000489692.1:p.Ile150=
ENST00000637432.1:c.5170A= ENSP00000490617.1:p.Ile1724=
ENST00000637736.1:c.5014A= ENSP00000489861.1:p.Ile1672=
ENST00000637769.1:c.5155A= ENSP00000489778.1:p.Ile1719=
ENST00000637777.1:c.346A=
ENST00000637809.1:n.545A=
ENST00000637819.1:c.556A= ENSP00000490686.1:p.Ile186=
ENST00000637832.1:n.146A=
ENST00000637927.1:c.5158A= ENSP00000489715.1:p.Ile1720=
ENST00000638009.2:c.5155A= ENSP00000489913.1:p.Ile1719=
ENST00000638029.1:c.5170A= ENSP00000489829.1:p.Ile1724=
ENST00000664864.1:c.5356A= ENSP00000499449.1:p.Ile1786=
ENST00000360228.9:c.5152A= ENSP00000353362.5:p.Ile1718=
ENST00000573710.6:c.5155A= ENSP00000460092.2:p.Ile1719=
ENST00000573891.5:c.571A=
ENST00000574822.5:n.376A=
ENST00000585802.5:c.1210A= ENSP00000465598.1:p.Ile404=
ENST00000587525.5:c.613A= ENSP00000467729.1:p.Ile205=
ENST00000593267.1:n.357A=
ENST00000614285.4:c.5170A= ENSP00000479983.1:p.Ile1724=
NM_000068.3:c.5170A= NP_000059.3:p.Ile1724=
NM_001127221.1:c.5155A= , LRG_7t1:c.5155A= NP_001120693.1:p.Ile1719=
NM_001127222.1:c.5152A= NP_001120694.1:p.Ile1718=
NM_001174080.1:c.5161A= NP_001167551.1:p.Ile1721=
NM_023035.2:c.5170A= NP_075461.2:p.Ile1724=
NM_000068.4:c.5170A= NP_000059.3:p.Ile1724=
NM_001127222.2:c.5152A= MANE Select NP_001120694.1:p.Ile1718=
NM_001174080.2:c.5161A= NP_001167551.1:p.Ile1721=
NM_023035.3:c.5170A= NP_075461.2:p.Ile1724=
NM_001127221.2:c.5155A= NP_001120693.1:p.Ile1719=