Canonical Allele Identifier: CA783430378

Gene: CACNA1A

Linked Data

• dbSNP Id: rs1277116613
• gnomAD v3: 19-13235390-G-C
• gnomAD v4: 19-13235390-G-C
• MyVariant Identifiers: chr19:g.13346204G>C (hg19) ; chr19:g.13235390G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13235390G>C , CM000681.2:g.13235390G>C	GRCh38
NC_000019.9:g.13346204G>C , CM000681.1:g.13346204G>C	GRCh37
NC_000019.8:g.13207204G>C	NCBI36
NG_011569.1:g.276071C>G , LRG_7:g.276071C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360228.11:c.5068-116C>G MANE Select	ENSP00000353362.5:n.5068-116C>G
ENST00000573710.7:c.5074-116C>G	ENSP00000460092.3:n.5074-116C>G
ENST00000573891.6:c.487-116C>G
ENST00000574822.6:n.292-116C>G
ENST00000585802.6:c.229-116C>G	ENSP00000465598.2:n.229-116C>G
ENST00000593267.2:n.273-116C>G
ENST00000635727.1:c.5071-116C>G	ENSP00000490001.1:n.5071-116C>G
ENST00000635742.1:n.1057-116C>G
ENST00000635895.1:c.5071-116C>G	ENSP00000490323.1:n.5071-116C>G
ENST00000636012.1:c.5071-116C>G	ENSP00000490223.1:n.5071-116C>G
ENST00000636058.1:c.383-116C>G
ENST00000636389.1:c.5071-116C>G	ENSP00000489992.1:n.5071-116C>G
ENST00000636473.1:c.228+224C>G	ENSP00000490173.1:n.228+224C>G
ENST00000636549.1:c.5077-116C>G	ENSP00000490578.1:n.5077-116C>G
ENST00000637276.1:c.5071-116C>G	ENSP00000489777.1:n.5071-116C>G
ENST00000637297.1:c.364-116C>G	ENSP00000489692.1:n.364-116C>G
ENST00000637432.1:c.5086-116C>G	ENSP00000490617.1:n.5086-116C>G
ENST00000637736.1:c.4930-116C>G	ENSP00000489861.1:n.4930-116C>G
ENST00000637769.1:c.5071-116C>G	ENSP00000489778.1:n.5071-116C>G
ENST00000637777.1:c.327+224C>G
ENST00000637809.1:n.461-116C>G
ENST00000637819.1:c.472-116C>G	ENSP00000490686.1:n.472-116C>G
ENST00000637832.1:n.62-116C>G
ENST00000637927.1:c.5074-116C>G	ENSP00000489715.1:n.5074-116C>G
ENST00000638009.2:c.5071-116C>G	ENSP00000489913.1:n.5071-116C>G
ENST00000638029.1:c.5086-116C>G	ENSP00000489829.1:n.5086-116C>G
ENST00000664864.1:c.5272-116C>G	ENSP00000499449.1:n.5272-116C>G
ENST00000360228.9:c.5068-116C>G	ENSP00000353362.5:n.5068-116C>G
ENST00000573710.6:c.5071-116C>G	ENSP00000460092.2:n.5071-116C>G
ENST00000573891.5:c.487-116C>G
ENST00000574822.5:n.292-116C>G
ENST00000585802.5:c.1126-116C>G	ENSP00000465598.1:n.1126-116C>G
ENST00000587525.5:c.529-116C>G	ENSP00000467729.1:n.529-116C>G
ENST00000593267.1:n.273-116C>G
ENST00000614285.4:c.5086-116C>G	ENSP00000479983.1:n.5086-116C>G
NM_000068.3:c.5086-116C>G	NP_000059.3:n.5086-116C>G
NM_001127221.1:c.5071-116C>G , LRG_7t1:c.5071-116C>G	NP_001120693.1:n.5071-116C>G
NM_001127222.1:c.5068-116C>G	NP_001120694.1:n.5068-116C>G
NM_001174080.1:c.5077-116C>G	NP_001167551.1:n.5077-116C>G
NM_023035.2:c.5086-116C>G	NP_075461.2:n.5086-116C>G
NM_000068.4:c.5086-116C>G	NP_000059.3:n.5086-116C>G
NM_001127222.2:c.5068-116C>G MANE Select	NP_001120694.1:n.5068-116C>G
NM_001174080.2:c.5077-116C>G	NP_001167551.1:n.5077-116C>G
NM_023035.3:c.5086-116C>G	NP_075461.2:n.5086-116C>G
NM_001127221.2:c.5071-116C>G	NP_001120693.1:n.5071-116C>G