Canonical Allele Identifier: CA404344014
Gene: CACNA1A HGNC NCBI

Linked Data

ClinVar Variation Id: 542827
ClinVar RCV Id: RCV000653332
dbSNP Id: rs1555756737

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13300638C>A , CM000681.2:g.13300638C>A GRCh38
NC_000019.9:g.13411452C>A , CM000681.1:g.13411452C>A GRCh37
NC_000019.8:g.13272452C>A NCBI36
NG_011569.1:g.210823G>T , LRG_7:g.210823G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360228.11:c.2191G>T MANE Select ENSP00000353362.5:p.Glu731Ter
ENST00000573710.7:c.2197G>T ENSP00000460092.3:p.Glu733Ter
ENST00000635727.1:c.2194G>T ENSP00000490001.1:p.Glu732Ter
ENST00000635895.1:c.2194G>T ENSP00000490323.1:p.Glu732Ter
ENST00000636012.1:c.2194G>T ENSP00000490223.1:p.Glu732Ter
ENST00000636389.1:c.2194G>T ENSP00000489992.1:p.Glu732Ter
ENST00000636549.1:c.2194G>T ENSP00000490578.1:p.Glu732Ter
ENST00000637276.1:c.2194G>T ENSP00000489777.1:p.Glu732Ter
ENST00000637432.1:c.2203G>T ENSP00000490617.1:p.Glu735Ter
ENST00000637736.1:c.2053G>T ENSP00000489861.1:p.Glu685Ter
ENST00000637769.1:c.2194G>T ENSP00000489778.1:p.Glu732Ter
ENST00000637927.1:c.2197G>T ENSP00000489715.1:p.Glu733Ter
ENST00000638009.2:c.2194G>T ENSP00000489913.1:p.Glu732Ter
ENST00000638029.1:c.2203G>T ENSP00000489829.1:p.Glu735Ter
ENST00000664864.1:c.2389G>T ENSP00000499449.1:p.Glu797Ter
ENST00000360228.9:c.2191G>T ENSP00000353362.5:p.Glu731Ter
ENST00000573710.6:c.2194G>T ENSP00000460092.2:p.Glu732Ter
ENST00000614285.4:c.2203G>T ENSP00000479983.1:p.Glu735Ter
NM_000068.3:c.2203G>T NP_000059.3:p.Glu735Ter
NM_001127221.1:c.2194G>T , LRG_7t1:c.2194G>T NP_001120693.1:p.Glu732Ter
NM_001127222.1:c.2191G>T NP_001120694.1:p.Glu731Ter
NM_001174080.1:c.2194G>T NP_001167551.1:p.Glu732Ter
NM_023035.2:c.2203G>T NP_075461.2:p.Glu735Ter
NM_000068.4:c.2203G>T NP_000059.3:p.Glu735Ter
NM_001127222.2:c.2191G>T MANE Select NP_001120694.1:p.Glu731Ter
NM_001174080.2:c.2194G>T NP_001167551.1:p.Glu732Ter
NM_023035.3:c.2203G>T NP_075461.2:p.Glu735Ter
NM_001127221.2:c.2194G>T NP_001120693.1:p.Glu732Ter