Canonical Allele Identifier: CA404339935

Gene: CACNA1A

Linked Data

• MyVariant Identifiers: chr19:g.13373561A>C (hg19) ; chr19:g.13262747A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13262747A>C , CM000681.2:g.13262747A>C	GRCh38
NC_000019.9:g.13373561A>C , CM000681.1:g.13373561A>C	GRCh37
NC_000019.8:g.13234561A>C	NCBI36
NG_011569.1:g.248714T>G , LRG_7:g.248714T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360228.11:c.4076T>G MANE Select	ENSP00000353362.5:p.Leu1359Arg
ENST00000573710.7:c.4082T>G	ENSP00000460092.3:p.Leu1361Arg
ENST00000635727.1:c.4079T>G	ENSP00000490001.1:p.Leu1360Arg
ENST00000635742.1:n.65T>G
ENST00000635895.1:c.4079T>G	ENSP00000490323.1:p.Leu1360Arg
ENST00000635917.1:n.568T>G
ENST00000636012.1:c.4079T>G	ENSP00000490223.1:p.Leu1360Arg
ENST00000636389.1:c.4079T>G	ENSP00000489992.1:p.Leu1360Arg
ENST00000636549.1:c.4079T>G	ENSP00000490578.1:p.Leu1360Arg
ENST00000636816.1:n.764T>G
ENST00000637004.1:n.542T>G
ENST00000637276.1:c.4079T>G	ENSP00000489777.1:p.Leu1360Arg
ENST00000637432.1:c.4088T>G	ENSP00000490617.1:p.Leu1363Arg
ENST00000637692.1:n.398T>G
ENST00000637736.1:c.3938T>G	ENSP00000489861.1:p.Leu1313Arg
ENST00000637769.1:c.4079T>G	ENSP00000489778.1:p.Leu1360Arg
ENST00000637927.1:c.4082T>G	ENSP00000489715.1:p.Leu1361Arg
ENST00000638009.2:c.4079T>G	ENSP00000489913.1:p.Leu1360Arg
ENST00000638029.1:c.4088T>G	ENSP00000489829.1:p.Leu1363Arg
ENST00000664864.1:c.4274T>G	ENSP00000499449.1:p.Leu1425Arg
ENST00000360228.9:c.4076T>G	ENSP00000353362.5:p.Leu1359Arg
ENST00000573710.6:c.4079T>G	ENSP00000460092.2:p.Leu1360Arg
ENST00000585802.5:c.134T>G	ENSP00000465598.1:p.Leu45Arg
ENST00000590205.1:n.155T>G
ENST00000614285.4:c.4088T>G	ENSP00000479983.1:p.Leu1363Arg
NM_000068.3:c.4088T>G	NP_000059.3:p.Leu1363Arg
NM_001127221.1:c.4079T>G , LRG_7t1:c.4079T>G	NP_001120693.1:p.Leu1360Arg
NM_001127222.1:c.4076T>G	NP_001120694.1:p.Leu1359Arg
NM_001174080.1:c.4079T>G	NP_001167551.1:p.Leu1360Arg
NM_023035.2:c.4088T>G	NP_075461.2:p.Leu1363Arg
NM_000068.4:c.4088T>G	NP_000059.3:p.Leu1363Arg
NM_001127222.2:c.4076T>G MANE Select	NP_001120694.1:p.Leu1359Arg
NM_001174080.2:c.4079T>G	NP_001167551.1:p.Leu1360Arg
NM_023035.3:c.4088T>G	NP_075461.2:p.Leu1363Arg
NM_001127221.2:c.4079T>G	NP_001120693.1:p.Leu1360Arg