Canonical Allele Identifier: CA16044236

Gene: CACNA1A

Linked Data

• ClinVar Variation Id: 375366
• ClinVar RCV Id: RCV000416438 ; RCV000556499 ; RCV002227158
• dbSNP Id: rs1057519429
• MyVariant Identifiers: chr19:g.13346480C>G (hg19) ; chr19:g.13235666C>G (hg38)
• PubMed: PMID:28327206

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13235666C>G , CM000681.2:g.13235666C>G	GRCh38
NC_000019.9:g.13346480C>G , CM000681.1:g.13346480C>G	GRCh37
NC_000019.8:g.13207480C>G	NCBI36
NG_011569.1:g.275795G>C , LRG_7:g.275795G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360228.11:c.5015G>C MANE Select	ENSP00000353362.5:p.Arg1672Pro
ENST00000573710.7:c.5021G>C	ENSP00000460092.3:p.Arg1674Pro
ENST00000573891.6:c.434G>C
ENST00000574822.6:n.239G>C
ENST00000585802.6:c.176G>C	ENSP00000465598.2:p.Arg59Pro
ENST00000593267.2:n.220G>C
ENST00000635727.1:c.5018G>C	ENSP00000490001.1:p.Arg1673Pro
ENST00000635742.1:n.1004G>C
ENST00000635895.1:c.5018G>C	ENSP00000490323.1:p.Arg1673Pro
ENST00000636012.1:c.5018G>C	ENSP00000490223.1:p.Arg1673Pro
ENST00000636058.1:c.330G>C
ENST00000636389.1:c.5018G>C	ENSP00000489992.1:p.Arg1673Pro
ENST00000636473.1:c.176G>C	ENSP00000490173.1:p.Arg59Pro
ENST00000636549.1:c.5024G>C	ENSP00000490578.1:p.Arg1675Pro
ENST00000637276.1:c.5018G>C	ENSP00000489777.1:p.Arg1673Pro
ENST00000637297.1:c.311G>C	ENSP00000489692.1:p.Arg104Pro
ENST00000637432.1:c.5033G>C	ENSP00000490617.1:p.Arg1678Pro
ENST00000637736.1:c.4877G>C	ENSP00000489861.1:p.Arg1626Pro
ENST00000637769.1:c.5018G>C	ENSP00000489778.1:p.Arg1673Pro
ENST00000637777.1:c.275G>C
ENST00000637809.1:n.408G>C
ENST00000637819.1:c.419G>C	ENSP00000490686.1:p.Arg140Pro
ENST00000637832.1:n.9G>C
ENST00000637927.1:c.5021G>C	ENSP00000489715.1:p.Arg1674Pro
ENST00000638009.2:c.5018G>C	ENSP00000489913.1:p.Arg1673Pro
ENST00000638029.1:c.5033G>C	ENSP00000489829.1:p.Arg1678Pro
ENST00000664864.1:c.5219G>C	ENSP00000499449.1:p.Arg1740Pro
ENST00000360228.9:c.5015G>C	ENSP00000353362.5:p.Arg1672Pro
ENST00000573710.6:c.5018G>C	ENSP00000460092.2:p.Arg1673Pro
ENST00000573891.5:c.434G>C
ENST00000574822.5:n.239G>C
ENST00000585802.5:c.1073G>C	ENSP00000465598.1:p.Arg358Pro
ENST00000587525.5:c.476G>C	ENSP00000467729.1:p.Arg159Pro
ENST00000593267.1:n.220G>C
ENST00000614285.4:c.5033G>C	ENSP00000479983.1:p.Arg1678Pro
NM_000068.3:c.5033G>C	NP_000059.3:p.Arg1678Pro
NM_001127221.1:c.5018G>C , LRG_7t1:c.5018G>C	NP_001120693.1:p.Arg1673Pro
NM_001127222.1:c.5015G>C	NP_001120694.1:p.Arg1672Pro
NM_001174080.1:c.5024G>C	NP_001167551.1:p.Arg1675Pro
NM_023035.2:c.5033G>C	NP_075461.2:p.Arg1678Pro
NM_000068.4:c.5033G>C	NP_000059.3:p.Arg1678Pro
NM_001127222.2:c.5015G>C MANE Select	NP_001120694.1:p.Arg1672Pro
NM_001174080.2:c.5024G>C	NP_001167551.1:p.Arg1675Pro
NM_023035.3:c.5033G>C	NP_075461.2:p.Arg1678Pro
NM_001127221.2:c.5018G>C	NP_001120693.1:p.Arg1673Pro