Canonical Allele Identifier: CA404339664

Gene: CACNA1A

Linked Data

• MyVariant Identifiers: chr19:g.13372322A>C (hg19) ; chr19:g.13261508A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13261508A>C , CM000681.2:g.13261508A>C	GRCh38
NC_000019.9:g.13372322A>C , CM000681.1:g.13372322A>C	GRCh37
NC_000019.8:g.13233322A>C	NCBI36
NG_011569.1:g.249953T>G , LRG_7:g.249953T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000360228.11:c.4192T>G MANE Select	ENSP00000353362.5:p.Phe1398Val
ENST00000573710.7:c.4198T>G	ENSP00000460092.3:p.Phe1400Val
ENST00000590205.2:n.1198T>G
ENST00000635727.1:c.4195T>G	ENSP00000490001.1:p.Phe1399Val
ENST00000635742.1:n.181T>G
ENST00000635895.1:c.4195T>G	ENSP00000490323.1:p.Phe1399Val
ENST00000635917.1:n.684T>G
ENST00000636012.1:c.4195T>G	ENSP00000490223.1:p.Phe1399Val
ENST00000636389.1:c.4195T>G	ENSP00000489992.1:p.Phe1399Val
ENST00000636549.1:c.4195T>G	ENSP00000490578.1:p.Phe1399Val
ENST00000636816.1:n.880T>G
ENST00000637004.1:n.658T>G
ENST00000637276.1:c.4195T>G	ENSP00000489777.1:p.Phe1399Val
ENST00000637432.1:c.4204T>G	ENSP00000490617.1:p.Phe1402Val
ENST00000637692.1:n.514T>G
ENST00000637736.1:c.4054T>G	ENSP00000489861.1:p.Phe1352Val
ENST00000637769.1:c.4195T>G	ENSP00000489778.1:p.Phe1399Val
ENST00000637927.1:c.4198T>G	ENSP00000489715.1:p.Phe1400Val
ENST00000638009.2:c.4195T>G	ENSP00000489913.1:p.Phe1399Val
ENST00000638029.1:c.4204T>G	ENSP00000489829.1:p.Phe1402Val
ENST00000664864.1:c.4390T>G	ENSP00000499449.1:p.Phe1464Val
ENST00000360228.9:c.4192T>G	ENSP00000353362.5:p.Phe1398Val
ENST00000573710.6:c.4195T>G	ENSP00000460092.2:p.Phe1399Val
ENST00000585802.5:c.250T>G	ENSP00000465598.1:p.Phe84Val
ENST00000590205.1:n.271T>G
ENST00000614285.4:c.4204T>G	ENSP00000479983.1:p.Phe1402Val
NM_000068.3:c.4204T>G	NP_000059.3:p.Phe1402Val
NM_001127221.1:c.4195T>G , LRG_7t1:c.4195T>G	NP_001120693.1:p.Phe1399Val
NM_001127222.1:c.4192T>G	NP_001120694.1:p.Phe1398Val
NM_001174080.1:c.4195T>G	NP_001167551.1:p.Phe1399Val
NM_023035.2:c.4204T>G	NP_075461.2:p.Phe1402Val
NM_000068.4:c.4204T>G	NP_000059.3:p.Phe1402Val
NM_001127222.2:c.4192T>G MANE Select	NP_001120694.1:p.Phe1398Val
NM_001174080.2:c.4195T>G	NP_001167551.1:p.Phe1399Val
NM_023035.3:c.4204T>G	NP_075461.2:p.Phe1402Val
NM_001127221.2:c.4195T>G	NP_001120693.1:p.Phe1399Val