Canonical Allele Identifier: CA404334960

Gene: CACNA1A

Linked Data

• MyVariant Identifiers: chr19:g.13342672C>A (hg19) ; chr19:g.13231858C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13231858C>A , CM000681.2:g.13231858C>A	GRCh38
NC_000019.9:g.13342672C>A , CM000681.1:g.13342672C>A	GRCh37
NC_000019.8:g.13203672C>A	NCBI36
NG_011569.1:g.279603G>T , LRG_7:g.279603G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360228.11:c.5252G>T MANE Select	ENSP00000353362.5:p.Ser1751Ile
ENST00000573710.7:c.5258G>T	ENSP00000460092.3:p.Ser1753Ile
ENST00000573891.6:c.671G>T
ENST00000574822.6:n.476G>T
ENST00000585802.6:c.413G>T	ENSP00000465598.2:p.Ser138Ile
ENST00000635727.1:c.5255G>T	ENSP00000490001.1:p.Ser1752Ile
ENST00000635742.1:n.1241G>T
ENST00000635895.1:c.5255G>T	ENSP00000490323.1:p.Ser1752Ile
ENST00000636012.1:c.5255G>T	ENSP00000490223.1:p.Ser1752Ile
ENST00000636058.1:c.567G>T
ENST00000636389.1:c.5255G>T	ENSP00000489992.1:p.Ser1752Ile
ENST00000636473.1:c.347G>T	ENSP00000490173.1:p.Ser116Ile
ENST00000636549.1:c.5261G>T	ENSP00000490578.1:p.Ser1754Ile
ENST00000637276.1:c.5255G>T	ENSP00000489777.1:p.Ser1752Ile
ENST00000637297.1:c.548G>T	ENSP00000489692.1:p.Ser183Ile
ENST00000637432.1:c.5270G>T	ENSP00000490617.1:p.Ser1757Ile
ENST00000637736.1:c.5114G>T	ENSP00000489861.1:p.Ser1705Ile
ENST00000637769.1:c.5255G>T	ENSP00000489778.1:p.Ser1752Ile
ENST00000637777.1:c.446G>T
ENST00000637809.1:n.645G>T
ENST00000637819.1:c.656G>T	ENSP00000490686.1:p.Ser219Ile
ENST00000637832.1:n.246G>T
ENST00000637927.1:c.5258G>T	ENSP00000489715.1:p.Ser1753Ile
ENST00000638009.2:c.5255G>T	ENSP00000489913.1:p.Ser1752Ile
ENST00000638029.1:c.5270G>T	ENSP00000489829.1:p.Ser1757Ile
ENST00000664864.1:c.5456G>T	ENSP00000499449.1:p.Ser1819Ile
ENST00000360228.9:c.5252G>T	ENSP00000353362.5:p.Ser1751Ile
ENST00000573710.6:c.5255G>T	ENSP00000460092.2:p.Ser1752Ile
ENST00000573891.5:c.671G>T
ENST00000574822.5:n.476G>T
ENST00000585802.5:c.1310G>T	ENSP00000465598.1:p.Ser437Ile
ENST00000587525.5:c.713G>T	ENSP00000467729.1:p.Ser238Ile
ENST00000614285.4:c.5270G>T	ENSP00000479983.1:p.Ser1757Ile
NM_000068.3:c.5270G>T	NP_000059.3:p.Ser1757Ile
NM_001127221.1:c.5255G>T , LRG_7t1:c.5255G>T	NP_001120693.1:p.Ser1752Ile
NM_001127222.1:c.5252G>T	NP_001120694.1:p.Ser1751Ile
NM_001174080.1:c.5261G>T	NP_001167551.1:p.Ser1754Ile
NM_023035.2:c.5270G>T	NP_075461.2:p.Ser1757Ile
NM_000068.4:c.5270G>T	NP_000059.3:p.Ser1757Ile
NM_001127222.2:c.5252G>T MANE Select	NP_001120694.1:p.Ser1751Ile
NM_001174080.2:c.5261G>T	NP_001167551.1:p.Ser1754Ile
NM_023035.3:c.5270G>T	NP_075461.2:p.Ser1757Ile
NM_001127221.2:c.5255G>T	NP_001120693.1:p.Ser1752Ile