Canonical Allele Identifier: CA16609419

Gene: CACNA1A

Linked Data

• ClinVar Variation Id: 397544
• ClinVar RCV Id: RCV000449585
• dbSNP Id: rs1060499675
• MyVariant Identifiers: chr19:g.13410054T>A (hg19) ; chr19:g.13299240T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13299240T>A , CM000681.2:g.13299240T>A	GRCh38
NC_000019.9:g.13410054T>A , CM000681.1:g.13410054T>A	GRCh37
NC_000019.8:g.13271054T>A	NCBI36
NG_011569.1:g.212221A>T , LRG_7:g.212221A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360228.11:c.2393A>T MANE Select	ENSP00000353362.5:p.Asp798Val
ENST00000573710.7:c.2399A>T	ENSP00000460092.3:p.Asp800Val
ENST00000635727.1:c.2396A>T	ENSP00000490001.1:p.Asp799Val
ENST00000635895.1:c.2396A>T	ENSP00000490323.1:p.Asp799Val
ENST00000636012.1:c.2396A>T	ENSP00000490223.1:p.Asp799Val
ENST00000636389.1:c.2396A>T	ENSP00000489992.1:p.Asp799Val
ENST00000636549.1:c.2396A>T	ENSP00000490578.1:p.Asp799Val
ENST00000637276.1:c.2396A>T	ENSP00000489777.1:p.Asp799Val
ENST00000637432.1:c.2405A>T	ENSP00000490617.1:p.Asp802Val
ENST00000637736.1:c.2255A>T	ENSP00000489861.1:p.Asp752Val
ENST00000637769.1:c.2396A>T	ENSP00000489778.1:p.Asp799Val
ENST00000637927.1:c.2399A>T	ENSP00000489715.1:p.Asp800Val
ENST00000638009.2:c.2396A>T	ENSP00000489913.1:p.Asp799Val
ENST00000638029.1:c.2405A>T	ENSP00000489829.1:p.Asp802Val
ENST00000664864.1:c.2591A>T	ENSP00000499449.1:p.Asp864Val
ENST00000360228.9:c.2393A>T	ENSP00000353362.5:p.Asp798Val
ENST00000573710.6:c.2396A>T	ENSP00000460092.2:p.Asp799Val
ENST00000614285.4:c.2405A>T	ENSP00000479983.1:p.Asp802Val
NM_000068.3:c.2405A>T	NP_000059.3:p.Asp802Val
NM_001127221.1:c.2396A>T , LRG_7t1:c.2396A>T	NP_001120693.1:p.Asp799Val
NM_001127222.1:c.2393A>T	NP_001120694.1:p.Asp798Val
NM_001174080.1:c.2396A>T	NP_001167551.1:p.Asp799Val
NM_023035.2:c.2405A>T	NP_075461.2:p.Asp802Val
NM_000068.4:c.2405A>T	NP_000059.3:p.Asp802Val
NM_001127222.2:c.2393A>T MANE Select	NP_001120694.1:p.Asp798Val
NM_001174080.2:c.2396A>T	NP_001167551.1:p.Asp799Val
NM_023035.3:c.2405A>T	NP_075461.2:p.Asp802Val
NM_001127221.2:c.2396A>T	NP_001120693.1:p.Asp799Val