Canonical Allele Identifier: CA404334942

Gene: CACNA1A

Linked Data

• MyVariant Identifiers: chr19:g.13342669G>A (hg19) ; chr19:g.13231855G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13231855G>A , CM000681.2:g.13231855G>A	GRCh38
NC_000019.9:g.13342669G>A , CM000681.1:g.13342669G>A	GRCh37
NC_000019.8:g.13203669G>A	NCBI36
NG_011569.1:g.279606C>T , LRG_7:g.279606C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360228.11:c.5255C>T MANE Select	ENSP00000353362.5:p.Ala1752Val
ENST00000573710.7:c.5261C>T	ENSP00000460092.3:p.Ala1754Val
ENST00000573891.6:c.674C>T
ENST00000574822.6:n.479C>T
ENST00000585802.6:c.416C>T	ENSP00000465598.2:p.Ala139Val
ENST00000635727.1:c.5258C>T	ENSP00000490001.1:p.Ala1753Val
ENST00000635742.1:n.1244C>T
ENST00000635895.1:c.5258C>T	ENSP00000490323.1:p.Ala1753Val
ENST00000636012.1:c.5258C>T	ENSP00000490223.1:p.Ala1753Val
ENST00000636058.1:c.570C>T
ENST00000636389.1:c.5258C>T	ENSP00000489992.1:p.Ala1753Val
ENST00000636473.1:c.350C>T	ENSP00000490173.1:p.Ala117Val
ENST00000636549.1:c.5264C>T	ENSP00000490578.1:p.Ala1755Val
ENST00000637276.1:c.5258C>T	ENSP00000489777.1:p.Ala1753Val
ENST00000637297.1:c.551C>T	ENSP00000489692.1:p.Ala184Val
ENST00000637432.1:c.5273C>T	ENSP00000490617.1:p.Ala1758Val
ENST00000637736.1:c.5117C>T	ENSP00000489861.1:p.Ala1706Val
ENST00000637769.1:c.5258C>T	ENSP00000489778.1:p.Ala1753Val
ENST00000637777.1:c.449C>T
ENST00000637809.1:n.648C>T
ENST00000637819.1:c.659C>T	ENSP00000490686.1:p.Ala220Val
ENST00000637832.1:n.249C>T
ENST00000637927.1:c.5261C>T	ENSP00000489715.1:p.Ala1754Val
ENST00000638009.2:c.5258C>T	ENSP00000489913.1:p.Ala1753Val
ENST00000638029.1:c.5273C>T	ENSP00000489829.1:p.Ala1758Val
ENST00000664864.1:c.5459C>T	ENSP00000499449.1:p.Ala1820Val
ENST00000360228.9:c.5255C>T	ENSP00000353362.5:p.Ala1752Val
ENST00000573710.6:c.5258C>T	ENSP00000460092.2:p.Ala1753Val
ENST00000573891.5:c.674C>T
ENST00000574822.5:n.479C>T
ENST00000585802.5:c.1313C>T	ENSP00000465598.1:p.Ala438Val
ENST00000587525.5:c.716C>T	ENSP00000467729.1:p.Ala239Val
ENST00000614285.4:c.5273C>T	ENSP00000479983.1:p.Ala1758Val
NM_000068.3:c.5273C>T	NP_000059.3:p.Ala1758Val
NM_001127221.1:c.5258C>T , LRG_7t1:c.5258C>T	NP_001120693.1:p.Ala1753Val
NM_001127222.1:c.5255C>T	NP_001120694.1:p.Ala1752Val
NM_001174080.1:c.5264C>T	NP_001167551.1:p.Ala1755Val
NM_023035.2:c.5273C>T	NP_075461.2:p.Ala1758Val
NM_000068.4:c.5273C>T	NP_000059.3:p.Ala1758Val
NM_001127222.2:c.5255C>T MANE Select	NP_001120694.1:p.Ala1752Val
NM_001174080.2:c.5264C>T	NP_001167551.1:p.Ala1755Val
NM_023035.3:c.5273C>T	NP_075461.2:p.Ala1758Val
NM_001127221.2:c.5258C>T	NP_001120693.1:p.Ala1753Val