Canonical Allele Identifier: CA404335806

Gene: CACNA1A

Linked Data

• MyVariant Identifiers: chr19:g.13346027A>G (hg19) ; chr19:g.13235213A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13235213A>G , CM000681.2:g.13235213A>G	GRCh38
NC_000019.9:g.13346027A>G , CM000681.1:g.13346027A>G	GRCh37
NC_000019.8:g.13207027A>G	NCBI36
NG_011569.1:g.276248T>C , LRG_7:g.276248T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360228.11:c.5129T>C MANE Select	ENSP00000353362.5:p.Met1710Thr
ENST00000573710.7:c.5135T>C	ENSP00000460092.3:p.Met1712Thr
ENST00000573891.6:c.548T>C
ENST00000574822.6:n.353T>C
ENST00000585802.6:c.290T>C	ENSP00000465598.2:p.Met97Thr
ENST00000593267.2:n.334T>C
ENST00000635727.1:c.5132T>C	ENSP00000490001.1:p.Met1711Thr
ENST00000635742.1:n.1118T>C
ENST00000635895.1:c.5132T>C	ENSP00000490323.1:p.Met1711Thr
ENST00000636012.1:c.5132T>C	ENSP00000490223.1:p.Met1711Thr
ENST00000636058.1:c.444T>C
ENST00000636389.1:c.5132T>C	ENSP00000489992.1:p.Met1711Thr
ENST00000636473.1:c.229-177T>C	ENSP00000490173.1:n.229-177T>C
ENST00000636549.1:c.5138T>C	ENSP00000490578.1:p.Met1713Thr
ENST00000637276.1:c.5132T>C	ENSP00000489777.1:p.Met1711Thr
ENST00000637297.1:c.425T>C	ENSP00000489692.1:p.Met142Thr
ENST00000637432.1:c.5147T>C	ENSP00000490617.1:p.Met1716Thr
ENST00000637736.1:c.4991T>C	ENSP00000489861.1:p.Met1664Thr
ENST00000637769.1:c.5132T>C	ENSP00000489778.1:p.Met1711Thr
ENST00000637777.1:c.328-177T>C
ENST00000637809.1:n.522T>C
ENST00000637819.1:c.533T>C	ENSP00000490686.1:p.Met178Thr
ENST00000637832.1:n.123T>C
ENST00000637927.1:c.5135T>C	ENSP00000489715.1:p.Met1712Thr
ENST00000638009.2:c.5132T>C	ENSP00000489913.1:p.Met1711Thr
ENST00000638029.1:c.5147T>C	ENSP00000489829.1:p.Met1716Thr
ENST00000664864.1:c.5333T>C	ENSP00000499449.1:p.Met1778Thr
ENST00000360228.9:c.5129T>C	ENSP00000353362.5:p.Met1710Thr
ENST00000573710.6:c.5132T>C	ENSP00000460092.2:p.Met1711Thr
ENST00000573891.5:c.548T>C
ENST00000574822.5:n.353T>C
ENST00000585802.5:c.1187T>C	ENSP00000465598.1:p.Met396Thr
ENST00000587525.5:c.590T>C	ENSP00000467729.1:p.Met197Thr
ENST00000593267.1:n.334T>C
ENST00000614285.4:c.5147T>C	ENSP00000479983.1:p.Met1716Thr
NM_000068.3:c.5147T>C	NP_000059.3:p.Met1716Thr
NM_001127221.1:c.5132T>C , LRG_7t1:c.5132T>C	NP_001120693.1:p.Met1711Thr
NM_001127222.1:c.5129T>C	NP_001120694.1:p.Met1710Thr
NM_001174080.1:c.5138T>C	NP_001167551.1:p.Met1713Thr
NM_023035.2:c.5147T>C	NP_075461.2:p.Met1716Thr
NM_000068.4:c.5147T>C	NP_000059.3:p.Met1716Thr
NM_001127222.2:c.5129T>C MANE Select	NP_001120694.1:p.Met1710Thr
NM_001174080.2:c.5138T>C	NP_001167551.1:p.Met1713Thr
NM_023035.3:c.5147T>C	NP_075461.2:p.Met1716Thr
NM_001127221.2:c.5132T>C	NP_001120693.1:p.Met1711Thr