Canonical Allele Identifier: CA2323795592
Gene: CACNA1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13235217C= , CM000681.2:g.13235217C= GRCh38
NC_000019.9:g.13346031C= , CM000681.1:g.13346031C= GRCh37
NC_000019.8:g.13207031C= NCBI36
NG_011569.1:g.276244G= , LRG_7:g.276244G=

Transcript Alleles

HGVS Amino-acid change
ENST00000360228.11:c.5125G= MANE Select ENSP00000353362.5:p.Gly1709=
ENST00000573710.7:c.5131G= ENSP00000460092.3:p.Gly1711=
ENST00000573891.6:c.544G=
ENST00000574822.6:n.349G=
ENST00000585802.6:c.286G= ENSP00000465598.2:p.Gly96=
ENST00000593267.2:n.330G=
ENST00000635727.1:c.5128G= ENSP00000490001.1:p.Gly1710=
ENST00000635742.1:n.1114G=
ENST00000635895.1:c.5128G= ENSP00000490323.1:p.Gly1710=
ENST00000636012.1:c.5128G= ENSP00000490223.1:p.Gly1710=
ENST00000636058.1:c.440G=
ENST00000636389.1:c.5128G= ENSP00000489992.1:p.Gly1710=
ENST00000636473.1:c.229-181G= ENSP00000490173.1:n.229-181G=
ENST00000636549.1:c.5134G= ENSP00000490578.1:p.Gly1712=
ENST00000637276.1:c.5128G= ENSP00000489777.1:p.Gly1710=
ENST00000637297.1:c.421G= ENSP00000489692.1:p.Gly141=
ENST00000637432.1:c.5143G= ENSP00000490617.1:p.Gly1715=
ENST00000637736.1:c.4987G= ENSP00000489861.1:p.Gly1663=
ENST00000637769.1:c.5128G= ENSP00000489778.1:p.Gly1710=
ENST00000637777.1:c.328-181G=
ENST00000637809.1:n.518G=
ENST00000637819.1:c.529G= ENSP00000490686.1:p.Gly177=
ENST00000637832.1:n.119G=
ENST00000637927.1:c.5131G= ENSP00000489715.1:p.Gly1711=
ENST00000638009.2:c.5128G= ENSP00000489913.1:p.Gly1710=
ENST00000638029.1:c.5143G= ENSP00000489829.1:p.Gly1715=
ENST00000664864.1:c.5329G= ENSP00000499449.1:p.Gly1777=
ENST00000360228.9:c.5125G= ENSP00000353362.5:p.Gly1709=
ENST00000573710.6:c.5128G= ENSP00000460092.2:p.Gly1710=
ENST00000573891.5:c.544G=
ENST00000574822.5:n.349G=
ENST00000585802.5:c.1183G= ENSP00000465598.1:p.Gly395=
ENST00000587525.5:c.586G= ENSP00000467729.1:p.Gly196=
ENST00000593267.1:n.330G=
ENST00000614285.4:c.5143G= ENSP00000479983.1:p.Gly1715=
NM_000068.3:c.5143G= NP_000059.3:p.Gly1715=
NM_001127221.1:c.5128G= , LRG_7t1:c.5128G= NP_001120693.1:p.Gly1710=
NM_001127222.1:c.5125G= NP_001120694.1:p.Gly1709=
NM_001174080.1:c.5134G= NP_001167551.1:p.Gly1712=
NM_023035.2:c.5143G= NP_075461.2:p.Gly1715=
NM_000068.4:c.5143G= NP_000059.3:p.Gly1715=
NM_001127222.2:c.5125G= MANE Select NP_001120694.1:p.Gly1709=
NM_001174080.2:c.5134G= NP_001167551.1:p.Gly1712=
NM_023035.3:c.5143G= NP_075461.2:p.Gly1715=
NM_001127221.2:c.5128G= NP_001120693.1:p.Gly1710=