Canonical Allele Identifier: CA2832576675
Gene: CACNA1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13261399_13261400dup , CM000681.2:g.13261399_13261400dup GRCh38
NC_000019.9:g.13372213_13372214dup , CM000681.1:g.13372213_13372214dup GRCh37
NC_000019.8:g.13233213_13233214dup NCBI36
NG_011569.1:g.250065_250066dup , LRG_7:g.250065_250066dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000360228.11:c.4250+54_4250+55dup MANE Select ENSP00000353362.5:n.4250+54_4250+55dup
ENST00000573710.7:c.4256+54_4256+55dup ENSP00000460092.3:n.4256+54_4256+55dup
ENST00000590205.2:n.1310_1311dup
ENST00000635727.1:c.4253+54_4253+55dup ENSP00000490001.1:n.4253+54_4253+55dup
ENST00000635742.1:n.239+54_239+55dup
ENST00000635895.1:c.4253+54_4253+55dup ENSP00000490323.1:n.4253+54_4253+55dup
ENST00000635917.1:n.742+54_742+55dup
ENST00000636012.1:c.4253+54_4253+55dup ENSP00000490223.1:n.4253+54_4253+55dup
ENST00000636389.1:c.4253+54_4253+55dup ENSP00000489992.1:n.4253+54_4253+55dup
ENST00000636549.1:c.4253+54_4253+55dup ENSP00000490578.1:n.4253+54_4253+55dup
ENST00000636816.1:n.938+54_938+55dup
ENST00000637004.1:n.716+54_716+55dup
ENST00000637276.1:c.4253+54_4253+55dup ENSP00000489777.1:n.4253+54_4253+55dup
ENST00000637432.1:c.4262+54_4262+55dup ENSP00000490617.1:n.4262+54_4262+55dup
ENST00000637692.1:n.572+54_572+55dup
ENST00000637736.1:c.4112+54_4112+55dup ENSP00000489861.1:n.4112+54_4112+55dup
ENST00000637769.1:c.4253+54_4253+55dup ENSP00000489778.1:n.4253+54_4253+55dup
ENST00000637927.1:c.4256+54_4256+55dup ENSP00000489715.1:n.4256+54_4256+55dup
ENST00000638009.2:c.4253+54_4253+55dup ENSP00000489913.1:n.4253+54_4253+55dup
ENST00000638029.1:c.4262+54_4262+55dup ENSP00000489829.1:n.4262+54_4262+55dup
ENST00000664864.1:c.4448+54_4448+55dup ENSP00000499449.1:n.4448+54_4448+55dup
ENST00000360228.9:c.4250+54_4250+55dup ENSP00000353362.5:n.4250+54_4250+55dup
ENST00000573710.6:c.4253+54_4253+55dup ENSP00000460092.2:n.4253+54_4253+55dup
ENST00000585802.5:c.308+54_308+55dup ENSP00000465598.1:n.308+54_308+55dup
ENST00000614285.4:c.4262+54_4262+55dup ENSP00000479983.1:n.4262+54_4262+55dup
NM_000068.3:c.4262+54_4262+55dup NP_000059.3:n.4262+54_4262+55dup
NM_001127221.1:c.4253+54_4253+55dup , LRG_7t1:c.4253+54_4253+55dup NP_001120693.1:n.4253+54_4253+55dup
NM_001127222.1:c.4250+54_4250+55dup NP_001120694.1:n.4250+54_4250+55dup
NM_001174080.1:c.4253+54_4253+55dup NP_001167551.1:n.4253+54_4253+55dup
NM_023035.2:c.4262+54_4262+55dup NP_075461.2:n.4262+54_4262+55dup
NM_000068.4:c.4262+54_4262+55dup NP_000059.3:n.4262+54_4262+55dup
NM_001127222.2:c.4250+54_4250+55dup MANE Select NP_001120694.1:n.4250+54_4250+55dup
NM_001174080.2:c.4253+54_4253+55dup NP_001167551.1:n.4253+54_4253+55dup
NM_023035.3:c.4262+54_4262+55dup NP_075461.2:n.4262+54_4262+55dup
NM_001127221.2:c.4253+54_4253+55dup NP_001120693.1:n.4253+54_4253+55dup