Canonical Allele Identifier: CA505658793

Gene: CACNA1A

Linked Data

• ClinVar Variation Id: 2952056
• ClinVar RCV Id: RCV003815207
• MyVariant Identifiers: chr19:g.13346497C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13235683C>A , CM000681.2:g.13235683C>A	GRCh38
NC_000019.9:g.13346497C>A , CM000681.1:g.13346497C>A	GRCh37
NC_000019.8:g.13207497C>A	NCBI36
NG_011569.1:g.275778G>T , LRG_7:g.275778G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360228.11:c.4998G>T MANE Select	ENSP00000353362.5:p.Arg1666=
ENST00000573710.7:c.5004G>T	ENSP00000460092.3:p.Arg1668=
ENST00000573891.6:c.417G>T
ENST00000574822.6:n.222G>T
ENST00000585802.6:c.159G>T	ENSP00000465598.2:p.Arg53=
ENST00000593267.2:n.203G>T
ENST00000635727.1:c.5001G>T	ENSP00000490001.1:p.Arg1667=
ENST00000635742.1:n.987G>T
ENST00000635895.1:c.5001G>T	ENSP00000490323.1:p.Arg1667=
ENST00000636012.1:c.5001G>T	ENSP00000490223.1:p.Arg1667=
ENST00000636058.1:c.313G>T
ENST00000636389.1:c.5001G>T	ENSP00000489992.1:p.Arg1667=
ENST00000636473.1:c.159G>T	ENSP00000490173.1:p.Arg53=
ENST00000636549.1:c.5007G>T	ENSP00000490578.1:p.Arg1669=
ENST00000637276.1:c.5001G>T	ENSP00000489777.1:p.Arg1667=
ENST00000637297.1:c.294G>T	ENSP00000489692.1:p.Arg98=
ENST00000637432.1:c.5016G>T	ENSP00000490617.1:p.Arg1672=
ENST00000637736.1:c.4860G>T	ENSP00000489861.1:p.Arg1620=
ENST00000637769.1:c.5001G>T	ENSP00000489778.1:p.Arg1667=
ENST00000637777.1:c.258G>T
ENST00000637809.1:n.391G>T
ENST00000637819.1:c.402G>T	ENSP00000490686.1:p.Arg134=
ENST00000637927.1:c.5004G>T	ENSP00000489715.1:p.Arg1668=
ENST00000638009.2:c.5001G>T	ENSP00000489913.1:p.Arg1667=
ENST00000638029.1:c.5016G>T	ENSP00000489829.1:p.Arg1672=
ENST00000664864.1:c.5202G>T	ENSP00000499449.1:p.Arg1734=
ENST00000360228.9:c.4998G>T	ENSP00000353362.5:p.Arg1666=
ENST00000573710.6:c.5001G>T	ENSP00000460092.2:p.Arg1667=
ENST00000573891.5:c.417G>T
ENST00000574822.5:n.222G>T
ENST00000585802.5:c.1056G>T	ENSP00000465598.1:p.Arg352=
ENST00000587525.5:c.459G>T	ENSP00000467729.1:p.Arg153=
ENST00000593267.1:n.203G>T
ENST00000614285.4:c.5016G>T	ENSP00000479983.1:p.Arg1672=
NM_000068.3:c.5016G>T	NP_000059.3:p.Arg1672=
NM_001127221.1:c.5001G>T , LRG_7t1:c.5001G>T	NP_001120693.1:p.Arg1667=
NM_001127222.1:c.4998G>T	NP_001120694.1:p.Arg1666=
NM_001174080.1:c.5007G>T	NP_001167551.1:p.Arg1669=
NM_023035.2:c.5016G>T	NP_075461.2:p.Arg1672=
NM_000068.4:c.5016G>T	NP_000059.3:p.Arg1672=
NM_001127222.2:c.4998G>T MANE Select	NP_001120694.1:p.Arg1666=
NM_001174080.2:c.5007G>T	NP_001167551.1:p.Arg1669=
NM_023035.3:c.5016G>T	NP_075461.2:p.Arg1672=
NM_001127221.2:c.5001G>T	NP_001120693.1:p.Arg1667=