Canonical Allele Identifier: CA404336562

Gene: CACNA1A

Linked Data

• MyVariant Identifiers: chr19:g.13346436A>T (hg19) ; chr19:g.13235622A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13235622A>T , CM000681.2:g.13235622A>T	GRCh38
NC_000019.9:g.13346436A>T , CM000681.1:g.13346436A>T	GRCh37
NC_000019.8:g.13207436A>T	NCBI36
NG_011569.1:g.275839T>A , LRG_7:g.275839T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360228.11:c.5059T>A MANE Select	ENSP00000353362.5:p.Ser1687Thr
ENST00000573710.7:c.5065T>A	ENSP00000460092.3:p.Ser1689Thr
ENST00000573891.6:c.478T>A
ENST00000574822.6:n.283T>A
ENST00000585802.6:c.220T>A	ENSP00000465598.2:p.Ser74Thr
ENST00000593267.2:n.264T>A
ENST00000635727.1:c.5062T>A	ENSP00000490001.1:p.Ser1688Thr
ENST00000635742.1:n.1048T>A
ENST00000635895.1:c.5062T>A	ENSP00000490323.1:p.Ser1688Thr
ENST00000636012.1:c.5062T>A	ENSP00000490223.1:p.Ser1688Thr
ENST00000636058.1:c.374T>A
ENST00000636389.1:c.5062T>A	ENSP00000489992.1:p.Ser1688Thr
ENST00000636473.1:c.220T>A	ENSP00000490173.1:p.Ser74Thr
ENST00000636549.1:c.5068T>A	ENSP00000490578.1:p.Ser1690Thr
ENST00000637276.1:c.5062T>A	ENSP00000489777.1:p.Ser1688Thr
ENST00000637297.1:c.355T>A	ENSP00000489692.1:p.Ser119Thr
ENST00000637432.1:c.5077T>A	ENSP00000490617.1:p.Ser1693Thr
ENST00000637736.1:c.4921T>A	ENSP00000489861.1:p.Ser1641Thr
ENST00000637769.1:c.5062T>A	ENSP00000489778.1:p.Ser1688Thr
ENST00000637777.1:c.319T>A
ENST00000637809.1:n.452T>A
ENST00000637819.1:c.463T>A	ENSP00000490686.1:p.Ser155Thr
ENST00000637832.1:n.53T>A
ENST00000637927.1:c.5065T>A	ENSP00000489715.1:p.Ser1689Thr
ENST00000638009.2:c.5062T>A	ENSP00000489913.1:p.Ser1688Thr
ENST00000638029.1:c.5077T>A	ENSP00000489829.1:p.Ser1693Thr
ENST00000664864.1:c.5263T>A	ENSP00000499449.1:p.Ser1755Thr
ENST00000360228.9:c.5059T>A	ENSP00000353362.5:p.Ser1687Thr
ENST00000573710.6:c.5062T>A	ENSP00000460092.2:p.Ser1688Thr
ENST00000573891.5:c.478T>A
ENST00000574822.5:n.283T>A
ENST00000585802.5:c.1117T>A	ENSP00000465598.1:p.Ser373Thr
ENST00000587525.5:c.520T>A	ENSP00000467729.1:p.Ser174Thr
ENST00000593267.1:n.264T>A
ENST00000614285.4:c.5077T>A	ENSP00000479983.1:p.Ser1693Thr
NM_000068.3:c.5077T>A	NP_000059.3:p.Ser1693Thr
NM_001127221.1:c.5062T>A , LRG_7t1:c.5062T>A	NP_001120693.1:p.Ser1688Thr
NM_001127222.1:c.5059T>A	NP_001120694.1:p.Ser1687Thr
NM_001174080.1:c.5068T>A	NP_001167551.1:p.Ser1690Thr
NM_023035.2:c.5077T>A	NP_075461.2:p.Ser1693Thr
NM_000068.4:c.5077T>A	NP_000059.3:p.Ser1693Thr
NM_001127222.2:c.5059T>A MANE Select	NP_001120694.1:p.Ser1687Thr
NM_001174080.2:c.5068T>A	NP_001167551.1:p.Ser1690Thr
NM_023035.3:c.5077T>A	NP_075461.2:p.Ser1693Thr
NM_001127221.2:c.5062T>A	NP_001120693.1:p.Ser1688Thr