Canonical Allele Identifier: CA2323795506
Gene: CACNA1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13235050G= , CM000681.2:g.13235050G= GRCh38
NC_000019.9:g.13345864G= , CM000681.1:g.13345864G= GRCh37
NC_000019.8:g.13206864G= NCBI36
NG_011569.1:g.276411C= , LRG_7:g.276411C=

Transcript Alleles

HGVS Amino-acid change
ENST00000360228.11:c.5134-14C= MANE Select ENSP00000353362.5:n.5134-14C=
ENST00000573710.7:c.5140-14C= ENSP00000460092.3:n.5140-14C=
ENST00000573891.6:c.553-14C=
ENST00000574822.6:n.358-14C=
ENST00000585802.6:c.295-14C= ENSP00000465598.2:n.295-14C=
ENST00000593267.2:n.339-14C=
ENST00000635727.1:c.5137-14C= ENSP00000490001.1:n.5137-14C=
ENST00000635742.1:n.1123-14C=
ENST00000635895.1:c.5137-14C= ENSP00000490323.1:n.5137-14C=
ENST00000636012.1:c.5137-14C= ENSP00000490223.1:n.5137-14C=
ENST00000636058.1:c.449-14C=
ENST00000636389.1:c.5137-14C= ENSP00000489992.1:n.5137-14C=
ENST00000636473.1:c.229-14C= ENSP00000490173.1:n.229-14C=
ENST00000636549.1:c.5143-14C= ENSP00000490578.1:n.5143-14C=
ENST00000637276.1:c.5137-14C= ENSP00000489777.1:n.5137-14C=
ENST00000637297.1:c.430-14C= ENSP00000489692.1:n.430-14C=
ENST00000637432.1:c.5152-14C= ENSP00000490617.1:n.5152-14C=
ENST00000637736.1:c.4996-14C= ENSP00000489861.1:n.4996-14C=
ENST00000637769.1:c.5137-14C= ENSP00000489778.1:n.5137-14C=
ENST00000637777.1:c.328-14C=
ENST00000637809.1:n.527-14C=
ENST00000637819.1:c.538-14C= ENSP00000490686.1:n.538-14C=
ENST00000637832.1:n.128-14C=
ENST00000637927.1:c.5140-14C= ENSP00000489715.1:n.5140-14C=
ENST00000638009.2:c.5137-14C= ENSP00000489913.1:n.5137-14C=
ENST00000638029.1:c.5152-14C= ENSP00000489829.1:n.5152-14C=
ENST00000664864.1:c.5338-14C= ENSP00000499449.1:n.5338-14C=
ENST00000360228.9:c.5134-14C= ENSP00000353362.5:n.5134-14C=
ENST00000573710.6:c.5137-14C= ENSP00000460092.2:n.5137-14C=
ENST00000573891.5:c.553-14C=
ENST00000574822.5:n.358-14C=
ENST00000585802.5:c.1192-14C= ENSP00000465598.1:n.1192-14C=
ENST00000587525.5:c.595-14C= ENSP00000467729.1:n.595-14C=
ENST00000593267.1:n.339-14C=
ENST00000614285.4:c.5152-14C= ENSP00000479983.1:n.5152-14C=
NM_000068.3:c.5152-14C= NP_000059.3:n.5152-14C=
NM_001127221.1:c.5137-14C= , LRG_7t1:c.5137-14C= NP_001120693.1:n.5137-14C=
NM_001127222.1:c.5134-14C= NP_001120694.1:n.5134-14C=
NM_001174080.1:c.5143-14C= NP_001167551.1:n.5143-14C=
NM_023035.2:c.5152-14C= NP_075461.2:n.5152-14C=
NM_000068.4:c.5152-14C= NP_000059.3:n.5152-14C=
NM_001127222.2:c.5134-14C= MANE Select NP_001120694.1:n.5134-14C=
NM_001174080.2:c.5143-14C= NP_001167551.1:n.5143-14C=
NM_023035.3:c.5152-14C= NP_075461.2:n.5152-14C=
NM_001127221.2:c.5137-14C= NP_001120693.1:n.5137-14C=