Canonical Allele Identifier: CA16620786

Gene: CACNA1A

Linked Data

• ClinVar Variation Id: 420945
• ClinVar RCV Id: RCV000486354 ; RCV000679938 ; RCV002227167 ; RCV003152605
• dbSNP Id: rs1064794808
• MyVariant Identifiers: chr19:g.13373582G>A (hg19) ; chr19:g.13262768G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13262768G>A , CM000681.2:g.13262768G>A	GRCh38
NC_000019.9:g.13373582G>A , CM000681.1:g.13373582G>A	GRCh37
NC_000019.8:g.13234582G>A	NCBI36
NG_011569.1:g.248693C>T , LRG_7:g.248693C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360228.11:c.4055C>T MANE Select	ENSP00000353362.5:p.Pro1352Leu
ENST00000573710.7:c.4061C>T	ENSP00000460092.3:p.Pro1354Leu
ENST00000635727.1:c.4058C>T	ENSP00000490001.1:p.Pro1353Leu
ENST00000635742.1:n.44C>T
ENST00000635895.1:c.4058C>T	ENSP00000490323.1:p.Pro1353Leu
ENST00000635917.1:n.547C>T
ENST00000636012.1:c.4058C>T	ENSP00000490223.1:p.Pro1353Leu
ENST00000636389.1:c.4058C>T	ENSP00000489992.1:p.Pro1353Leu
ENST00000636549.1:c.4058C>T	ENSP00000490578.1:p.Pro1353Leu
ENST00000636816.1:n.743C>T
ENST00000637004.1:n.521C>T
ENST00000637276.1:c.4058C>T	ENSP00000489777.1:p.Pro1353Leu
ENST00000637432.1:c.4067C>T	ENSP00000490617.1:p.Pro1356Leu
ENST00000637692.1:n.377C>T
ENST00000637736.1:c.3917C>T	ENSP00000489861.1:p.Pro1306Leu
ENST00000637769.1:c.4058C>T	ENSP00000489778.1:p.Pro1353Leu
ENST00000637927.1:c.4061C>T	ENSP00000489715.1:p.Pro1354Leu
ENST00000638009.2:c.4058C>T	ENSP00000489913.1:p.Pro1353Leu
ENST00000638029.1:c.4067C>T	ENSP00000489829.1:p.Pro1356Leu
ENST00000664864.1:c.4253C>T	ENSP00000499449.1:p.Pro1418Leu
ENST00000360228.9:c.4055C>T	ENSP00000353362.5:p.Pro1352Leu
ENST00000573710.6:c.4058C>T	ENSP00000460092.2:p.Pro1353Leu
ENST00000585802.5:c.113C>T	ENSP00000465598.1:p.Pro38Leu
ENST00000590205.1:n.134C>T
ENST00000614285.4:c.4067C>T	ENSP00000479983.1:p.Pro1356Leu
NM_000068.3:c.4067C>T	NP_000059.3:p.Pro1356Leu
NM_001127221.1:c.4058C>T , LRG_7t1:c.4058C>T	NP_001120693.1:p.Pro1353Leu
NM_001127222.1:c.4055C>T	NP_001120694.1:p.Pro1352Leu
NM_001174080.1:c.4058C>T	NP_001167551.1:p.Pro1353Leu
NM_023035.2:c.4067C>T	NP_075461.2:p.Pro1356Leu
NM_000068.4:c.4067C>T	NP_000059.3:p.Pro1356Leu
NM_001127222.2:c.4055C>T MANE Select	NP_001120694.1:p.Pro1352Leu
NM_001174080.2:c.4058C>T	NP_001167551.1:p.Pro1353Leu
NM_023035.3:c.4067C>T	NP_075461.2:p.Pro1356Leu
NM_001127221.2:c.4058C>T	NP_001120693.1:p.Pro1353Leu