Canonical Allele Identifier: CA2323793821
Gene: CACNA1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13231866G= , CM000681.2:g.13231866G= GRCh38
NC_000019.9:g.13342680G= , CM000681.1:g.13342680G= GRCh37
NC_000019.8:g.13203680G= NCBI36
NG_011569.1:g.279595C= , LRG_7:g.279595C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360228.11:c.5250-6C= MANE Select ENSP00000353362.5:n.5250-6C=
ENST00000573710.7:c.5256-6C= ENSP00000460092.3:n.5256-6C=
ENST00000573891.6:c.669-6C=
ENST00000574822.6:n.474-6C=
ENST00000585802.6:c.411-6C= ENSP00000465598.2:n.411-6C=
ENST00000635727.1:c.5253-6C= ENSP00000490001.1:n.5253-6C=
ENST00000635742.1:n.1239-6C=
ENST00000635895.1:c.5253-6C= ENSP00000490323.1:n.5253-6C=
ENST00000636012.1:c.5253-6C= ENSP00000490223.1:n.5253-6C=
ENST00000636058.1:c.565-6C=
ENST00000636389.1:c.5253-6C= ENSP00000489992.1:n.5253-6C=
ENST00000636473.1:c.345-6C= ENSP00000490173.1:n.345-6C=
ENST00000636549.1:c.5259-6C= ENSP00000490578.1:n.5259-6C=
ENST00000637276.1:c.5253-6C= ENSP00000489777.1:n.5253-6C=
ENST00000637297.1:c.546-6C= ENSP00000489692.1:n.546-6C=
ENST00000637432.1:c.5268-6C= ENSP00000490617.1:n.5268-6C=
ENST00000637736.1:c.5112-6C= ENSP00000489861.1:n.5112-6C=
ENST00000637769.1:c.5253-6C= ENSP00000489778.1:n.5253-6C=
ENST00000637777.1:c.444-6C=
ENST00000637809.1:n.643-6C=
ENST00000637819.1:c.654-6C= ENSP00000490686.1:n.654-6C=
ENST00000637832.1:n.244-6C=
ENST00000637927.1:c.5256-6C= ENSP00000489715.1:n.5256-6C=
ENST00000638009.2:c.5253-6C= ENSP00000489913.1:n.5253-6C=
ENST00000638029.1:c.5268-6C= ENSP00000489829.1:n.5268-6C=
ENST00000664864.1:c.5454-6C= ENSP00000499449.1:n.5454-6C=
ENST00000360228.9:c.5250-6C= ENSP00000353362.5:n.5250-6C=
ENST00000573710.6:c.5253-6C= ENSP00000460092.2:n.5253-6C=
ENST00000573891.5:c.669-6C=
ENST00000574822.5:n.474-6C=
ENST00000585802.5:c.1308-6C= ENSP00000465598.1:n.1308-6C=
ENST00000587525.5:c.711-6C= ENSP00000467729.1:n.711-6C=
ENST00000614285.4:c.5268-6C= ENSP00000479983.1:n.5268-6C=
NM_000068.3:c.5268-6C= NP_000059.3:n.5268-6C=
NM_001127221.1:c.5253-6C= , LRG_7t1:c.5253-6C= NP_001120693.1:n.5253-6C=
NM_001127222.1:c.5250-6C= NP_001120694.1:n.5250-6C=
NM_001174080.1:c.5259-6C= NP_001167551.1:n.5259-6C=
NM_023035.2:c.5268-6C= NP_075461.2:n.5268-6C=
NM_000068.4:c.5268-6C= NP_000059.3:n.5268-6C=
NM_001127222.2:c.5250-6C= MANE Select NP_001120694.1:n.5250-6C=
NM_001174080.2:c.5259-6C= NP_001167551.1:n.5259-6C=
NM_023035.3:c.5268-6C= NP_075461.2:n.5268-6C=
NM_001127221.2:c.5253-6C= NP_001120693.1:n.5253-6C=