Canonical Allele Identifier: CA2323795770
Gene: CACNA1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13235650G= , CM000681.2:g.13235650G= GRCh38
NC_000019.9:g.13346464G= , CM000681.1:g.13346464G= GRCh37
NC_000019.8:g.13207464G= NCBI36
NG_011569.1:g.275811C= , LRG_7:g.275811C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360228.11:c.5031C= MANE Select ENSP00000353362.5:p.Ile1677=
ENST00000573710.7:c.5037C= ENSP00000460092.3:p.Ile1679=
ENST00000573891.6:c.450C=
ENST00000574822.6:n.255C=
ENST00000585802.6:c.192C= ENSP00000465598.2:p.Ile64=
ENST00000593267.2:n.236C=
ENST00000635727.1:c.5034C= ENSP00000490001.1:p.Ile1678=
ENST00000635742.1:n.1020C=
ENST00000635895.1:c.5034C= ENSP00000490323.1:p.Ile1678=
ENST00000636012.1:c.5034C= ENSP00000490223.1:p.Ile1678=
ENST00000636058.1:c.346C=
ENST00000636389.1:c.5034C= ENSP00000489992.1:p.Ile1678=
ENST00000636473.1:c.192C= ENSP00000490173.1:p.Ile64=
ENST00000636549.1:c.5040C= ENSP00000490578.1:p.Ile1680=
ENST00000637276.1:c.5034C= ENSP00000489777.1:p.Ile1678=
ENST00000637297.1:c.327C= ENSP00000489692.1:p.Ile109=
ENST00000637432.1:c.5049C= ENSP00000490617.1:p.Ile1683=
ENST00000637736.1:c.4893C= ENSP00000489861.1:p.Ile1631=
ENST00000637769.1:c.5034C= ENSP00000489778.1:p.Ile1678=
ENST00000637777.1:c.291C=
ENST00000637809.1:n.424C=
ENST00000637819.1:c.435C= ENSP00000490686.1:p.Ile145=
ENST00000637832.1:n.25C=
ENST00000637927.1:c.5037C= ENSP00000489715.1:p.Ile1679=
ENST00000638009.2:c.5034C= ENSP00000489913.1:p.Ile1678=
ENST00000638029.1:c.5049C= ENSP00000489829.1:p.Ile1683=
ENST00000664864.1:c.5235C= ENSP00000499449.1:p.Ile1745=
ENST00000360228.9:c.5031C= ENSP00000353362.5:p.Ile1677=
ENST00000573710.6:c.5034C= ENSP00000460092.2:p.Ile1678=
ENST00000573891.5:c.450C=
ENST00000574822.5:n.255C=
ENST00000585802.5:c.1089C= ENSP00000465598.1:p.Ile363=
ENST00000587525.5:c.492C= ENSP00000467729.1:p.Ile164=
ENST00000593267.1:n.236C=
ENST00000614285.4:c.5049C= ENSP00000479983.1:p.Ile1683=
NM_000068.3:c.5049C= NP_000059.3:p.Ile1683=
NM_001127221.1:c.5034C= , LRG_7t1:c.5034C= NP_001120693.1:p.Ile1678=
NM_001127222.1:c.5031C= NP_001120694.1:p.Ile1677=
NM_001174080.1:c.5040C= NP_001167551.1:p.Ile1680=
NM_023035.2:c.5049C= NP_075461.2:p.Ile1683=
NM_000068.4:c.5049C= NP_000059.3:p.Ile1683=
NM_001127222.2:c.5031C= MANE Select NP_001120694.1:p.Ile1677=
NM_001174080.2:c.5040C= NP_001167551.1:p.Ile1680=
NM_023035.3:c.5049C= NP_075461.2:p.Ile1683=
NM_001127221.2:c.5034C= NP_001120693.1:p.Ile1678=