Canonical Allele Identifier: CA505658560

Gene: CACNA1A

Linked Data

• gnomAD v4: 19-13235224-G-T
• MyVariant Identifiers: chr19:g.13346038G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13235224G>T , CM000681.2:g.13235224G>T	GRCh38
NC_000019.9:g.13346038G>T , CM000681.1:g.13346038G>T	GRCh37
NC_000019.8:g.13207038G>T	NCBI36
NG_011569.1:g.276237C>A , LRG_7:g.276237C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000360228.11:c.5118C>A MANE Select	ENSP00000353362.5:p.Ala1706=
ENST00000573710.7:c.5124C>A	ENSP00000460092.3:p.Ala1708=
ENST00000573891.6:c.537C>A
ENST00000574822.6:n.342C>A
ENST00000585802.6:c.279C>A	ENSP00000465598.2:p.Ala93=
ENST00000593267.2:n.323C>A
ENST00000635727.1:c.5121C>A	ENSP00000490001.1:p.Ala1707=
ENST00000635742.1:n.1107C>A
ENST00000635895.1:c.5121C>A	ENSP00000490323.1:p.Ala1707=
ENST00000636012.1:c.5121C>A	ENSP00000490223.1:p.Ala1707=
ENST00000636058.1:c.433C>A
ENST00000636389.1:c.5121C>A	ENSP00000489992.1:p.Ala1707=
ENST00000636473.1:c.229-188C>A	ENSP00000490173.1:n.229-188C>A
ENST00000636549.1:c.5127C>A	ENSP00000490578.1:p.Ala1709=
ENST00000637276.1:c.5121C>A	ENSP00000489777.1:p.Ala1707=
ENST00000637297.1:c.414C>A	ENSP00000489692.1:p.Ala138=
ENST00000637432.1:c.5136C>A	ENSP00000490617.1:p.Ala1712=
ENST00000637736.1:c.4980C>A	ENSP00000489861.1:p.Ala1660=
ENST00000637769.1:c.5121C>A	ENSP00000489778.1:p.Ala1707=
ENST00000637777.1:c.328-188C>A
ENST00000637809.1:n.511C>A
ENST00000637819.1:c.522C>A	ENSP00000490686.1:p.Ala174=
ENST00000637832.1:n.112C>A
ENST00000637927.1:c.5124C>A	ENSP00000489715.1:p.Ala1708=
ENST00000638009.2:c.5121C>A	ENSP00000489913.1:p.Ala1707=
ENST00000638029.1:c.5136C>A	ENSP00000489829.1:p.Ala1712=
ENST00000664864.1:c.5322C>A	ENSP00000499449.1:p.Ala1774=
ENST00000360228.9:c.5118C>A	ENSP00000353362.5:p.Ala1706=
ENST00000573710.6:c.5121C>A	ENSP00000460092.2:p.Ala1707=
ENST00000573891.5:c.537C>A
ENST00000574822.5:n.342C>A
ENST00000585802.5:c.1176C>A	ENSP00000465598.1:p.Ala392=
ENST00000587525.5:c.579C>A	ENSP00000467729.1:p.Ala193=
ENST00000593267.1:n.323C>A
ENST00000614285.4:c.5136C>A	ENSP00000479983.1:p.Ala1712=
NM_000068.3:c.5136C>A	NP_000059.3:p.Ala1712=
NM_001127221.1:c.5121C>A , LRG_7t1:c.5121C>A	NP_001120693.1:p.Ala1707=
NM_001127222.1:c.5118C>A	NP_001120694.1:p.Ala1706=
NM_001174080.1:c.5127C>A	NP_001167551.1:p.Ala1709=
NM_023035.2:c.5136C>A	NP_075461.2:p.Ala1712=
NM_000068.4:c.5136C>A	NP_000059.3:p.Ala1712=
NM_001127222.2:c.5118C>A MANE Select	NP_001120694.1:p.Ala1706=
NM_001174080.2:c.5127C>A	NP_001167551.1:p.Ala1709=
NM_023035.3:c.5136C>A	NP_075461.2:p.Ala1712=
NM_001127221.2:c.5121C>A	NP_001120693.1:p.Ala1707=