Canonical Allele Identifier: CA505658811

Gene: CACNA1A

Linked Data

• MyVariant Identifiers: chr19:g.13346512G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13235698G>C , CM000681.2:g.13235698G>C	GRCh38
NC_000019.9:g.13346512G>C , CM000681.1:g.13346512G>C	GRCh37
NC_000019.8:g.13207512G>C	NCBI36
NG_011569.1:g.275763C>G , LRG_7:g.275763C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000360228.11:c.4983C>G MANE Select	ENSP00000353362.5:p.Leu1661=
ENST00000573710.7:c.4989C>G	ENSP00000460092.3:p.Leu1663=
ENST00000573891.6:c.402C>G
ENST00000574822.6:n.207C>G
ENST00000585802.6:c.144C>G	ENSP00000465598.2:p.Leu48=
ENST00000593267.2:n.188C>G
ENST00000635727.1:c.4986C>G	ENSP00000490001.1:p.Leu1662=
ENST00000635742.1:n.972C>G
ENST00000635895.1:c.4986C>G	ENSP00000490323.1:p.Leu1662=
ENST00000636012.1:c.4986C>G	ENSP00000490223.1:p.Leu1662=
ENST00000636058.1:c.298C>G
ENST00000636389.1:c.4986C>G	ENSP00000489992.1:p.Leu1662=
ENST00000636473.1:c.144C>G	ENSP00000490173.1:p.Leu48=
ENST00000636549.1:c.4992C>G	ENSP00000490578.1:p.Leu1664=
ENST00000637276.1:c.4986C>G	ENSP00000489777.1:p.Leu1662=
ENST00000637297.1:c.279C>G	ENSP00000489692.1:p.Leu93=
ENST00000637432.1:c.5001C>G	ENSP00000490617.1:p.Leu1667=
ENST00000637736.1:c.4845C>G	ENSP00000489861.1:p.Leu1615=
ENST00000637769.1:c.4986C>G	ENSP00000489778.1:p.Leu1662=
ENST00000637777.1:c.243C>G
ENST00000637809.1:n.376C>G
ENST00000637819.1:c.387C>G	ENSP00000490686.1:p.Leu129=
ENST00000637927.1:c.4989C>G	ENSP00000489715.1:p.Leu1663=
ENST00000638009.2:c.4986C>G	ENSP00000489913.1:p.Leu1662=
ENST00000638029.1:c.5001C>G	ENSP00000489829.1:p.Leu1667=
ENST00000664864.1:c.5187C>G	ENSP00000499449.1:p.Leu1729=
ENST00000360228.9:c.4983C>G	ENSP00000353362.5:p.Leu1661=
ENST00000573710.6:c.4986C>G	ENSP00000460092.2:p.Leu1662=
ENST00000573891.5:c.402C>G
ENST00000574822.5:n.207C>G
ENST00000585802.5:c.1041C>G	ENSP00000465598.1:p.Leu347=
ENST00000587525.5:c.444C>G	ENSP00000467729.1:p.Leu148=
ENST00000593267.1:n.188C>G
ENST00000614285.4:c.5001C>G	ENSP00000479983.1:p.Leu1667=
NM_000068.3:c.5001C>G	NP_000059.3:p.Leu1667=
NM_001127221.1:c.4986C>G , LRG_7t1:c.4986C>G	NP_001120693.1:p.Leu1662=
NM_001127222.1:c.4983C>G	NP_001120694.1:p.Leu1661=
NM_001174080.1:c.4992C>G	NP_001167551.1:p.Leu1664=
NM_023035.2:c.5001C>G	NP_075461.2:p.Leu1667=
NM_000068.4:c.5001C>G	NP_000059.3:p.Leu1667=
NM_001127222.2:c.4983C>G MANE Select	NP_001120694.1:p.Leu1661=
NM_001174080.2:c.4992C>G	NP_001167551.1:p.Leu1664=
NM_023035.3:c.5001C>G	NP_075461.2:p.Leu1667=
NM_001127221.2:c.4986C>G	NP_001120693.1:p.Leu1662=