Canonical Allele Identifier: CA2323795763
Gene: CACNA1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13235629A= , CM000681.2:g.13235629A= GRCh38
NC_000019.9:g.13346443A= , CM000681.1:g.13346443A= GRCh37
NC_000019.8:g.13207443A= NCBI36
NG_011569.1:g.275832T= , LRG_7:g.275832T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360228.11:c.5052T= MANE Select ENSP00000353362.5:p.Phe1684=
ENST00000573710.7:c.5058T= ENSP00000460092.3:p.Phe1686=
ENST00000573891.6:c.471T=
ENST00000574822.6:n.276T=
ENST00000585802.6:c.213T= ENSP00000465598.2:p.Phe71=
ENST00000593267.2:n.257T=
ENST00000635727.1:c.5055T= ENSP00000490001.1:p.Phe1685=
ENST00000635742.1:n.1041T=
ENST00000635895.1:c.5055T= ENSP00000490323.1:p.Phe1685=
ENST00000636012.1:c.5055T= ENSP00000490223.1:p.Phe1685=
ENST00000636058.1:c.367T=
ENST00000636389.1:c.5055T= ENSP00000489992.1:p.Phe1685=
ENST00000636473.1:c.213T= ENSP00000490173.1:p.Phe71=
ENST00000636549.1:c.5061T= ENSP00000490578.1:p.Phe1687=
ENST00000637276.1:c.5055T= ENSP00000489777.1:p.Phe1685=
ENST00000637297.1:c.348T= ENSP00000489692.1:p.Phe116=
ENST00000637432.1:c.5070T= ENSP00000490617.1:p.Phe1690=
ENST00000637736.1:c.4914T= ENSP00000489861.1:p.Phe1638=
ENST00000637769.1:c.5055T= ENSP00000489778.1:p.Phe1685=
ENST00000637777.1:c.312T=
ENST00000637809.1:n.445T=
ENST00000637819.1:c.456T= ENSP00000490686.1:p.Phe152=
ENST00000637832.1:n.46T=
ENST00000637927.1:c.5058T= ENSP00000489715.1:p.Phe1686=
ENST00000638009.2:c.5055T= ENSP00000489913.1:p.Phe1685=
ENST00000638029.1:c.5070T= ENSP00000489829.1:p.Phe1690=
ENST00000664864.1:c.5256T= ENSP00000499449.1:p.Phe1752=
ENST00000360228.9:c.5052T= ENSP00000353362.5:p.Phe1684=
ENST00000573710.6:c.5055T= ENSP00000460092.2:p.Phe1685=
ENST00000573891.5:c.471T=
ENST00000574822.5:n.276T=
ENST00000585802.5:c.1110T= ENSP00000465598.1:p.Phe370=
ENST00000587525.5:c.513T= ENSP00000467729.1:p.Phe171=
ENST00000593267.1:n.257T=
ENST00000614285.4:c.5070T= ENSP00000479983.1:p.Phe1690=
NM_000068.3:c.5070T= NP_000059.3:p.Phe1690=
NM_001127221.1:c.5055T= , LRG_7t1:c.5055T= NP_001120693.1:p.Phe1685=
NM_001127222.1:c.5052T= NP_001120694.1:p.Phe1684=
NM_001174080.1:c.5061T= NP_001167551.1:p.Phe1687=
NM_023035.2:c.5070T= NP_075461.2:p.Phe1690=
NM_000068.4:c.5070T= NP_000059.3:p.Phe1690=
NM_001127222.2:c.5052T= MANE Select NP_001120694.1:p.Phe1684=
NM_001174080.2:c.5061T= NP_001167551.1:p.Phe1687=
NM_023035.3:c.5070T= NP_075461.2:p.Phe1690=
NM_001127221.2:c.5055T= NP_001120693.1:p.Phe1685=