Canonical Allele Identifier: CA404335804

Gene: CACNA1A

Linked Data

• MyVariant Identifiers: chr19:g.13346026C>G (hg19) ; chr19:g.13235212C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13235212C>G , CM000681.2:g.13235212C>G	GRCh38
NC_000019.9:g.13346026C>G , CM000681.1:g.13346026C>G	GRCh37
NC_000019.8:g.13207026C>G	NCBI36
NG_011569.1:g.276249G>C , LRG_7:g.276249G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360228.11:c.5130G>C MANE Select	ENSP00000353362.5:p.Met1710Ile
ENST00000573710.7:c.5136G>C	ENSP00000460092.3:p.Met1712Ile
ENST00000573891.6:c.549G>C
ENST00000574822.6:n.354G>C
ENST00000585802.6:c.291G>C	ENSP00000465598.2:p.Met97Ile
ENST00000593267.2:n.335G>C
ENST00000635727.1:c.5133G>C	ENSP00000490001.1:p.Met1711Ile
ENST00000635742.1:n.1119G>C
ENST00000635895.1:c.5133G>C	ENSP00000490323.1:p.Met1711Ile
ENST00000636012.1:c.5133G>C	ENSP00000490223.1:p.Met1711Ile
ENST00000636058.1:c.445G>C
ENST00000636389.1:c.5133G>C	ENSP00000489992.1:p.Met1711Ile
ENST00000636473.1:c.229-176G>C	ENSP00000490173.1:n.229-176G>C
ENST00000636549.1:c.5139G>C	ENSP00000490578.1:p.Met1713Ile
ENST00000637276.1:c.5133G>C	ENSP00000489777.1:p.Met1711Ile
ENST00000637297.1:c.426G>C	ENSP00000489692.1:p.Met142Ile
ENST00000637432.1:c.5148G>C	ENSP00000490617.1:p.Met1716Ile
ENST00000637736.1:c.4992G>C	ENSP00000489861.1:p.Met1664Ile
ENST00000637769.1:c.5133G>C	ENSP00000489778.1:p.Met1711Ile
ENST00000637777.1:c.328-176G>C
ENST00000637809.1:n.523G>C
ENST00000637819.1:c.534G>C	ENSP00000490686.1:p.Met178Ile
ENST00000637832.1:n.124G>C
ENST00000637927.1:c.5136G>C	ENSP00000489715.1:p.Met1712Ile
ENST00000638009.2:c.5133G>C	ENSP00000489913.1:p.Met1711Ile
ENST00000638029.1:c.5148G>C	ENSP00000489829.1:p.Met1716Ile
ENST00000664864.1:c.5334G>C	ENSP00000499449.1:p.Met1778Ile
ENST00000360228.9:c.5130G>C	ENSP00000353362.5:p.Met1710Ile
ENST00000573710.6:c.5133G>C	ENSP00000460092.2:p.Met1711Ile
ENST00000573891.5:c.549G>C
ENST00000574822.5:n.354G>C
ENST00000585802.5:c.1188G>C	ENSP00000465598.1:p.Met396Ile
ENST00000587525.5:c.591G>C	ENSP00000467729.1:p.Met197Ile
ENST00000593267.1:n.335G>C
ENST00000614285.4:c.5148G>C	ENSP00000479983.1:p.Met1716Ile
NM_000068.3:c.5148G>C	NP_000059.3:p.Met1716Ile
NM_001127221.1:c.5133G>C , LRG_7t1:c.5133G>C	NP_001120693.1:p.Met1711Ile
NM_001127222.1:c.5130G>C	NP_001120694.1:p.Met1710Ile
NM_001174080.1:c.5139G>C	NP_001167551.1:p.Met1713Ile
NM_023035.2:c.5148G>C	NP_075461.2:p.Met1716Ile
NM_000068.4:c.5148G>C	NP_000059.3:p.Met1716Ile
NM_001127222.2:c.5130G>C MANE Select	NP_001120694.1:p.Met1710Ile
NM_001174080.2:c.5139G>C	NP_001167551.1:p.Met1713Ile
NM_023035.3:c.5148G>C	NP_075461.2:p.Met1716Ile
NM_001127221.2:c.5133G>C	NP_001120693.1:p.Met1711Ile