Canonical Allele Identifier: CA2323859980
Gene: CACNA1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13371330_13371331delinsTG , CM000681.2:g.13371330_13371331delinsTG GRCh38
NC_000019.9:g.13482144_13482145delinsTG , CM000681.1:g.13482144_13482145delinsTG GRCh37
NC_000019.8:g.13343144_13343145delinsTG NCBI36
NG_011569.1:g.140130_140131delinsCA , LRG_7:g.140130_140131delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000360228.11:c.631+357_631+358delinsCA MANE Select ENSP00000353362.5:n.631+357_631+358delinsCA
ENST00000573710.7:c.631+357_631+358delinsCA ENSP00000460092.3:n.631+357_631+358delinsCA
ENST00000593160.2:n.346+357_346+358delinsCA
ENST00000635727.1:c.631+357_631+358delinsCA ENSP00000490001.1:n.631+357_631+358delinsCA
ENST00000635895.1:c.631+357_631+358delinsCA ENSP00000490323.1:n.631+357_631+358delinsCA
ENST00000636012.1:c.631+357_631+358delinsCA ENSP00000490223.1:n.631+357_631+358delinsCA
ENST00000636389.1:c.631+357_631+358delinsCA ENSP00000489992.1:n.631+357_631+358delinsCA
ENST00000636549.1:c.631+357_631+358delinsCA ENSP00000490578.1:n.631+357_631+358delinsCA
ENST00000636966.1:n.519+357_519+358delinsCA
ENST00000637276.1:c.631+357_631+358delinsCA ENSP00000489777.1:n.631+357_631+358delinsCA
ENST00000637432.1:c.631+357_631+358delinsCA ENSP00000490617.1:n.631+357_631+358delinsCA
ENST00000637736.1:c.490+357_490+358delinsCA ENSP00000489861.1:n.490+357_490+358delinsCA
ENST00000637769.1:c.631+357_631+358delinsCA ENSP00000489778.1:n.631+357_631+358delinsCA
ENST00000637927.1:c.631+357_631+358delinsCA ENSP00000489715.1:n.631+357_631+358delinsCA
ENST00000637966.1:n.484+357_484+358delinsCA
ENST00000637981.1:n.806_807delinsCA
ENST00000638009.2:c.631+357_631+358delinsCA ENSP00000489913.1:n.631+357_631+358delinsCA
ENST00000638029.1:c.631+357_631+358delinsCA ENSP00000489829.1:n.631+357_631+358delinsCA
ENST00000664864.1:c.826+357_826+358delinsCA ENSP00000499449.1:n.826+357_826+358delinsCA
ENST00000360228.9:c.631+357_631+358delinsCA ENSP00000353362.5:n.631+357_631+358delinsCA
ENST00000573710.6:c.631+357_631+358delinsCA ENSP00000460092.2:n.631+357_631+358delinsCA
ENST00000614285.4:c.631+357_631+358delinsCA ENSP00000479983.1:n.631+357_631+358delinsCA
NM_000068.3:c.631+357_631+358delinsCA NP_000059.3:n.631+357_631+358delinsCA
NM_001127221.1:c.631+357_631+358delinsCA , LRG_7t1:c.631+357_631+358delinsCA NP_001120693.1:n.631+357_631+358delinsCA
NM_001127222.1:c.631+357_631+358delinsCA NP_001120694.1:n.631+357_631+358delinsCA
NM_001174080.1:c.631+357_631+358delinsCA NP_001167551.1:n.631+357_631+358delinsCA
NM_023035.2:c.631+357_631+358delinsCA NP_075461.2:n.631+357_631+358delinsCA
NM_000068.4:c.631+357_631+358delinsCA NP_000059.3:n.631+357_631+358delinsCA
NM_001127222.2:c.631+357_631+358delinsCA MANE Select NP_001120694.1:n.631+357_631+358delinsCA
NM_001174080.2:c.631+357_631+358delinsCA NP_001167551.1:n.631+357_631+358delinsCA
NM_023035.3:c.631+357_631+358delinsCA NP_075461.2:n.631+357_631+358delinsCA
NM_001127221.2:c.631+357_631+358delinsCA NP_001120693.1:n.631+357_631+358delinsCA