Canonical Allele Identifier: CA305562470
Gene: CACNA1A HGNC NCBI

Linked Data

dbSNP Id: rs745865181

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13371944C>T , CM000681.2:g.13371944C>T GRCh38
NC_000019.9:g.13482758C>T , CM000681.1:g.13482758C>T GRCh37
NC_000019.8:g.13343758C>T NCBI36
NG_011569.1:g.139517G>A , LRG_7:g.139517G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360228.11:c.540-165G>A MANE Select ENSP00000353362.5:n.540-165G>A
ENST00000573710.7:c.540-165G>A ENSP00000460092.3:n.540-165G>A
ENST00000574974.3:c.*172-165G>A ENSP00000459963.2:n.*172-165G>A
ENST00000593160.2:n.255-165G>A
ENST00000635727.1:c.540-165G>A ENSP00000490001.1:n.540-165G>A
ENST00000635895.1:c.540-165G>A ENSP00000490323.1:n.540-165G>A
ENST00000636012.1:c.540-165G>A ENSP00000490223.1:n.540-165G>A
ENST00000636389.1:c.540-165G>A ENSP00000489992.1:n.540-165G>A
ENST00000636549.1:c.540-165G>A ENSP00000490578.1:n.540-165G>A
ENST00000636966.1:n.428-165G>A
ENST00000637276.1:c.540-165G>A ENSP00000489777.1:n.540-165G>A
ENST00000637432.1:c.540-165G>A ENSP00000490617.1:n.540-165G>A
ENST00000637736.1:c.399-165G>A ENSP00000489861.1:n.399-165G>A
ENST00000637769.1:c.540-165G>A ENSP00000489778.1:n.540-165G>A
ENST00000637927.1:c.540-165G>A ENSP00000489715.1:n.540-165G>A
ENST00000637966.1:n.393-165G>A
ENST00000637981.1:n.358-165G>A
ENST00000638009.2:c.540-165G>A ENSP00000489913.1:n.540-165G>A
ENST00000638029.1:c.540-165G>A ENSP00000489829.1:n.540-165G>A
ENST00000664864.1:c.735-165G>A ENSP00000499449.1:n.735-165G>A
ENST00000360228.9:c.540-165G>A ENSP00000353362.5:n.540-165G>A
ENST00000573710.6:c.540-165G>A ENSP00000460092.2:n.540-165G>A
ENST00000574974.1:c.291-165G>A ENSP00000459963.1:n.291-165G>A
ENST00000614285.4:c.540-165G>A ENSP00000479983.1:n.540-165G>A
NM_000068.3:c.540-165G>A NP_000059.3:n.540-165G>A
NM_001127221.1:c.540-165G>A , LRG_7t1:c.540-165G>A NP_001120693.1:n.540-165G>A
NM_001127222.1:c.540-165G>A NP_001120694.1:n.540-165G>A
NM_001174080.1:c.540-165G>A NP_001167551.1:n.540-165G>A
NM_023035.2:c.540-165G>A NP_075461.2:n.540-165G>A
NM_000068.4:c.540-165G>A NP_000059.3:n.540-165G>A
NM_001127222.2:c.540-165G>A MANE Select NP_001120694.1:n.540-165G>A
NM_001174080.2:c.540-165G>A NP_001167551.1:n.540-165G>A
NM_023035.3:c.540-165G>A NP_075461.2:n.540-165G>A
NM_001127221.2:c.540-165G>A NP_001120693.1:n.540-165G>A