Canonical Allele Identifier: CA305548162

Gene: CACNA1A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13209387G>A , CM000681.2:g.13209387G>A	GRCh38
NC_000019.9:g.13320201G>A , CM000681.1:g.13320201G>A	GRCh37
NC_000019.8:g.13181201G>A	NCBI36
NG_011569.1:g.302074C>T , LRG_7:g.302074C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001127222.2:c.6451C>T MANE Select	NP_001120694.1:p.His2151Tyr
ENST00000360228.11:c.6451C>T MANE Select	ENSP00000353362.5:p.His2151Tyr
NM_000068.3:c.6469C>T	NP_000059.3:p.His2157Tyr
NM_000068.4:c.6469C>T	NP_000059.3:p.His2157Tyr
NM_001127221.1:c.6454C>T , LRG_7t1:c.6454C>T	NP_001120693.1:p.His2152Tyr
NM_001127221.2:c.6454C>T	NP_001120693.1:p.His2152Tyr
NM_001127222.1:c.6451C>T	NP_001120694.1:p.His2151Tyr
NM_001174080.1:c.6460C>T	NP_001167551.1:p.His2154Tyr
NM_001174080.2:c.6460C>T	NP_001167551.1:p.His2154Tyr
NM_023035.2:c.6469C>T	NP_075461.2:p.His2157Tyr
NM_023035.3:c.6469C>T	NP_075461.2:p.His2157Tyr
ENST00000360228.9:c.6451C>T	ENSP00000353362.5:p.His2151Tyr
ENST00000573710.6:c.6454C>T	ENSP00000460092.2:p.His2152Tyr
ENST00000573710.7:c.6457C>T	ENSP00000460092.3:p.His2153Tyr
ENST00000585802.5:c.2473C>T	ENSP00000465598.1:p.His825Tyr
ENST00000585802.6:c.1576C>T	ENSP00000465598.2:p.His526Tyr
ENST00000587525.5:c.1876C>T	ENSP00000467729.1:p.His626Tyr
ENST00000614285.4:c.6469C>T	ENSP00000479983.1:p.His2157Tyr
ENST00000635727.1:c.6454C>T	ENSP00000490001.1:p.His2152Tyr
ENST00000635895.1:c.6454C>T	ENSP00000490323.1:p.His2152Tyr
ENST00000636012.1:c.6418C>T	ENSP00000490223.1:p.His2140Tyr
ENST00000636389.1:c.6454C>T	ENSP00000489992.1:p.His2152Tyr
ENST00000636473.1:c.1321C>T	ENSP00000490173.1:p.His441Tyr
ENST00000636549.1:c.6460C>T	ENSP00000490578.1:p.His2154Tyr
ENST00000636610.1:n.2818C>T
ENST00000636768.1:c.945C>T	ENSP00000490190.1:n.945C>T
ENST00000637276.1:c.6418C>T	ENSP00000489777.1:p.His2140Tyr
ENST00000637432.1:c.6469C>T	ENSP00000490617.1:p.His2157Tyr
ENST00000637736.1:c.6313C>T	ENSP00000489861.1:p.His2105Tyr
ENST00000637769.1:c.6454C>T	ENSP00000489778.1:p.His2152Tyr
ENST00000637927.1:c.6457C>T	ENSP00000489715.1:p.His2153Tyr
ENST00000638009.2:c.6454C>T	ENSP00000489913.1:p.His2152Tyr
ENST00000638029.1:c.6469C>T	ENSP00000489829.1:p.His2157Tyr
ENST00000664864.1:c.6655C>T	ENSP00000499449.1:p.His2219Tyr