Canonical Allele Identifier: CA404335833

Gene: CACNA1A

Linked Data

• gnomAD v4: 19-13235226-C-A
• MyVariant Identifiers: chr19:g.13346040C>A (hg19) ; chr19:g.13235226C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13235226C>A , CM000681.2:g.13235226C>A	GRCh38
NC_000019.9:g.13346040C>A , CM000681.1:g.13346040C>A	GRCh37
NC_000019.8:g.13207040C>A	NCBI36
NG_011569.1:g.276235G>T , LRG_7:g.276235G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360228.11:c.5116G>T MANE Select	ENSP00000353362.5:p.Ala1706Ser
ENST00000573710.7:c.5122G>T	ENSP00000460092.3:p.Ala1708Ser
ENST00000573891.6:c.535G>T
ENST00000574822.6:n.340G>T
ENST00000585802.6:c.277G>T	ENSP00000465598.2:p.Ala93Ser
ENST00000593267.2:n.321G>T
ENST00000635727.1:c.5119G>T	ENSP00000490001.1:p.Ala1707Ser
ENST00000635742.1:n.1105G>T
ENST00000635895.1:c.5119G>T	ENSP00000490323.1:p.Ala1707Ser
ENST00000636012.1:c.5119G>T	ENSP00000490223.1:p.Ala1707Ser
ENST00000636058.1:c.431G>T
ENST00000636389.1:c.5119G>T	ENSP00000489992.1:p.Ala1707Ser
ENST00000636473.1:c.229-190G>T	ENSP00000490173.1:n.229-190G>T
ENST00000636549.1:c.5125G>T	ENSP00000490578.1:p.Ala1709Ser
ENST00000637276.1:c.5119G>T	ENSP00000489777.1:p.Ala1707Ser
ENST00000637297.1:c.412G>T	ENSP00000489692.1:p.Ala138Ser
ENST00000637432.1:c.5134G>T	ENSP00000490617.1:p.Ala1712Ser
ENST00000637736.1:c.4978G>T	ENSP00000489861.1:p.Ala1660Ser
ENST00000637769.1:c.5119G>T	ENSP00000489778.1:p.Ala1707Ser
ENST00000637777.1:c.328-190G>T
ENST00000637809.1:n.509G>T
ENST00000637819.1:c.520G>T	ENSP00000490686.1:p.Ala174Ser
ENST00000637832.1:n.110G>T
ENST00000637927.1:c.5122G>T	ENSP00000489715.1:p.Ala1708Ser
ENST00000638009.2:c.5119G>T	ENSP00000489913.1:p.Ala1707Ser
ENST00000638029.1:c.5134G>T	ENSP00000489829.1:p.Ala1712Ser
ENST00000664864.1:c.5320G>T	ENSP00000499449.1:p.Ala1774Ser
ENST00000360228.9:c.5116G>T	ENSP00000353362.5:p.Ala1706Ser
ENST00000573710.6:c.5119G>T	ENSP00000460092.2:p.Ala1707Ser
ENST00000573891.5:c.535G>T
ENST00000574822.5:n.340G>T
ENST00000585802.5:c.1174G>T	ENSP00000465598.1:p.Ala392Ser
ENST00000587525.5:c.577G>T	ENSP00000467729.1:p.Ala193Ser
ENST00000593267.1:n.321G>T
ENST00000614285.4:c.5134G>T	ENSP00000479983.1:p.Ala1712Ser
NM_000068.3:c.5134G>T	NP_000059.3:p.Ala1712Ser
NM_001127221.1:c.5119G>T , LRG_7t1:c.5119G>T	NP_001120693.1:p.Ala1707Ser
NM_001127222.1:c.5116G>T	NP_001120694.1:p.Ala1706Ser
NM_001174080.1:c.5125G>T	NP_001167551.1:p.Ala1709Ser
NM_023035.2:c.5134G>T	NP_075461.2:p.Ala1712Ser
NM_000068.4:c.5134G>T	NP_000059.3:p.Ala1712Ser
NM_001127222.2:c.5116G>T MANE Select	NP_001120694.1:p.Ala1706Ser
NM_001174080.2:c.5125G>T	NP_001167551.1:p.Ala1709Ser
NM_023035.3:c.5134G>T	NP_075461.2:p.Ala1712Ser
NM_001127221.2:c.5119G>T	NP_001120693.1:p.Ala1707Ser