Canonical Allele Identifier: CA404339995

Gene: CACNA1A

Linked Data

• MyVariant Identifiers: chr19:g.13373591A>G (hg19) ; chr19:g.13262777A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13262777A>G , CM000681.2:g.13262777A>G	GRCh38
NC_000019.9:g.13373591A>G , CM000681.1:g.13373591A>G	GRCh37
NC_000019.8:g.13234591A>G	NCBI36
NG_011569.1:g.248684T>C , LRG_7:g.248684T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360228.11:c.4046T>C MANE Select	ENSP00000353362.5:p.Val1349Ala
ENST00000573710.7:c.4052T>C	ENSP00000460092.3:p.Val1351Ala
ENST00000635727.1:c.4049T>C	ENSP00000490001.1:p.Val1350Ala
ENST00000635742.1:n.35T>C
ENST00000635895.1:c.4049T>C	ENSP00000490323.1:p.Val1350Ala
ENST00000635917.1:n.538T>C
ENST00000636012.1:c.4049T>C	ENSP00000490223.1:p.Val1350Ala
ENST00000636389.1:c.4049T>C	ENSP00000489992.1:p.Val1350Ala
ENST00000636549.1:c.4049T>C	ENSP00000490578.1:p.Val1350Ala
ENST00000636816.1:n.734T>C
ENST00000637004.1:n.512T>C
ENST00000637276.1:c.4049T>C	ENSP00000489777.1:p.Val1350Ala
ENST00000637432.1:c.4058T>C	ENSP00000490617.1:p.Val1353Ala
ENST00000637692.1:n.368T>C
ENST00000637736.1:c.3908T>C	ENSP00000489861.1:p.Val1303Ala
ENST00000637769.1:c.4049T>C	ENSP00000489778.1:p.Val1350Ala
ENST00000637927.1:c.4052T>C	ENSP00000489715.1:p.Val1351Ala
ENST00000638009.2:c.4049T>C	ENSP00000489913.1:p.Val1350Ala
ENST00000638029.1:c.4058T>C	ENSP00000489829.1:p.Val1353Ala
ENST00000664864.1:c.4244T>C	ENSP00000499449.1:p.Val1415Ala
ENST00000360228.9:c.4046T>C	ENSP00000353362.5:p.Val1349Ala
ENST00000573710.6:c.4049T>C	ENSP00000460092.2:p.Val1350Ala
ENST00000585802.5:c.104T>C	ENSP00000465598.1:p.Val35Ala
ENST00000590205.1:n.125T>C
ENST00000614285.4:c.4058T>C	ENSP00000479983.1:p.Val1353Ala
NM_000068.3:c.4058T>C	NP_000059.3:p.Val1353Ala
NM_001127221.1:c.4049T>C , LRG_7t1:c.4049T>C	NP_001120693.1:p.Val1350Ala
NM_001127222.1:c.4046T>C	NP_001120694.1:p.Val1349Ala
NM_001174080.1:c.4049T>C	NP_001167551.1:p.Val1350Ala
NM_023035.2:c.4058T>C	NP_075461.2:p.Val1353Ala
NM_000068.4:c.4058T>C	NP_000059.3:p.Val1353Ala
NM_001127222.2:c.4046T>C MANE Select	NP_001120694.1:p.Val1349Ala
NM_001174080.2:c.4049T>C	NP_001167551.1:p.Val1350Ala
NM_023035.3:c.4058T>C	NP_075461.2:p.Val1353Ala
NM_001127221.2:c.4049T>C	NP_001120693.1:p.Val1350Ala