Canonical Allele Identifier: CA505658453

Gene: CACNA1A

Linked Data

• dbSNP Id: rs2144646929
• MyVariant Identifiers: chr19:g.13345842A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13235028A>G , CM000681.2:g.13235028A>G	GRCh38
NC_000019.9:g.13345842A>G , CM000681.1:g.13345842A>G	GRCh37
NC_000019.8:g.13206842A>G	NCBI36
NG_011569.1:g.276433T>C , LRG_7:g.276433T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360228.11:c.5142T>C MANE Select	ENSP00000353362.5:p.Gly1714=
ENST00000573710.7:c.5148T>C	ENSP00000460092.3:p.Gly1716=
ENST00000573891.6:c.561T>C
ENST00000574822.6:n.366T>C
ENST00000585802.6:c.303T>C	ENSP00000465598.2:p.Gly101=
ENST00000593267.2:n.347T>C
ENST00000635727.1:c.5145T>C	ENSP00000490001.1:p.Gly1715=
ENST00000635742.1:n.1131T>C
ENST00000635895.1:c.5145T>C	ENSP00000490323.1:p.Gly1715=
ENST00000636012.1:c.5145T>C	ENSP00000490223.1:p.Gly1715=
ENST00000636058.1:c.457T>C
ENST00000636389.1:c.5145T>C	ENSP00000489992.1:p.Gly1715=
ENST00000636473.1:c.237T>C	ENSP00000490173.1:p.Gly79=
ENST00000636549.1:c.5151T>C	ENSP00000490578.1:p.Gly1717=
ENST00000637276.1:c.5145T>C	ENSP00000489777.1:p.Gly1715=
ENST00000637297.1:c.438T>C	ENSP00000489692.1:p.Gly146=
ENST00000637432.1:c.5160T>C	ENSP00000490617.1:p.Gly1720=
ENST00000637736.1:c.5004T>C	ENSP00000489861.1:p.Gly1668=
ENST00000637769.1:c.5145T>C	ENSP00000489778.1:p.Gly1715=
ENST00000637777.1:c.336T>C
ENST00000637809.1:n.535T>C
ENST00000637819.1:c.546T>C	ENSP00000490686.1:p.Gly182=
ENST00000637832.1:n.136T>C
ENST00000637927.1:c.5148T>C	ENSP00000489715.1:p.Gly1716=
ENST00000638009.2:c.5145T>C	ENSP00000489913.1:p.Gly1715=
ENST00000638029.1:c.5160T>C	ENSP00000489829.1:p.Gly1720=
ENST00000664864.1:c.5346T>C	ENSP00000499449.1:p.Gly1782=
ENST00000360228.9:c.5142T>C	ENSP00000353362.5:p.Gly1714=
ENST00000573710.6:c.5145T>C	ENSP00000460092.2:p.Gly1715=
ENST00000573891.5:c.561T>C
ENST00000574822.5:n.366T>C
ENST00000585802.5:c.1200T>C	ENSP00000465598.1:p.Gly400=
ENST00000587525.5:c.603T>C	ENSP00000467729.1:p.Gly201=
ENST00000593267.1:n.347T>C
ENST00000614285.4:c.5160T>C	ENSP00000479983.1:p.Gly1720=
NM_000068.3:c.5160T>C	NP_000059.3:p.Gly1720=
NM_001127221.1:c.5145T>C , LRG_7t1:c.5145T>C	NP_001120693.1:p.Gly1715=
NM_001127222.1:c.5142T>C	NP_001120694.1:p.Gly1714=
NM_001174080.1:c.5151T>C	NP_001167551.1:p.Gly1717=
NM_023035.2:c.5160T>C	NP_075461.2:p.Gly1720=
NM_000068.4:c.5160T>C	NP_000059.3:p.Gly1720=
NM_001127222.2:c.5142T>C MANE Select	NP_001120694.1:p.Gly1714=
NM_001174080.2:c.5151T>C	NP_001167551.1:p.Gly1717=
NM_023035.3:c.5160T>C	NP_075461.2:p.Gly1720=
NM_001127221.2:c.5145T>C	NP_001120693.1:p.Gly1715=