Canonical Allele Identifier: CA2323795691
Gene: CACNA1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13235443C= , CM000681.2:g.13235443C= GRCh38
NC_000019.9:g.13346257C= , CM000681.1:g.13346257C= GRCh37
NC_000019.8:g.13207257C= NCBI36
NG_011569.1:g.276018G= , LRG_7:g.276018G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360228.11:c.5068-169G= MANE Select ENSP00000353362.5:n.5068-169G=
ENST00000573710.7:c.5074-169G= ENSP00000460092.3:n.5074-169G=
ENST00000573891.6:c.487-169G=
ENST00000574822.6:n.292-169G=
ENST00000585802.6:c.229-169G= ENSP00000465598.2:n.229-169G=
ENST00000593267.2:n.273-169G=
ENST00000635727.1:c.5071-169G= ENSP00000490001.1:n.5071-169G=
ENST00000635742.1:n.1057-169G=
ENST00000635895.1:c.5071-169G= ENSP00000490323.1:n.5071-169G=
ENST00000636012.1:c.5071-169G= ENSP00000490223.1:n.5071-169G=
ENST00000636058.1:c.383-169G=
ENST00000636389.1:c.5071-169G= ENSP00000489992.1:n.5071-169G=
ENST00000636473.1:c.228+171G= ENSP00000490173.1:n.228+171G=
ENST00000636549.1:c.5077-169G= ENSP00000490578.1:n.5077-169G=
ENST00000637276.1:c.5071-169G= ENSP00000489777.1:n.5071-169G=
ENST00000637297.1:c.364-169G= ENSP00000489692.1:n.364-169G=
ENST00000637432.1:c.5086-169G= ENSP00000490617.1:n.5086-169G=
ENST00000637736.1:c.4930-169G= ENSP00000489861.1:n.4930-169G=
ENST00000637769.1:c.5071-169G= ENSP00000489778.1:n.5071-169G=
ENST00000637777.1:c.327+171G=
ENST00000637809.1:n.461-169G=
ENST00000637819.1:c.472-169G= ENSP00000490686.1:n.472-169G=
ENST00000637832.1:n.62-169G=
ENST00000637927.1:c.5074-169G= ENSP00000489715.1:n.5074-169G=
ENST00000638009.2:c.5071-169G= ENSP00000489913.1:n.5071-169G=
ENST00000638029.1:c.5086-169G= ENSP00000489829.1:n.5086-169G=
ENST00000664864.1:c.5272-169G= ENSP00000499449.1:n.5272-169G=
ENST00000360228.9:c.5068-169G= ENSP00000353362.5:n.5068-169G=
ENST00000573710.6:c.5071-169G= ENSP00000460092.2:n.5071-169G=
ENST00000573891.5:c.487-169G=
ENST00000574822.5:n.292-169G=
ENST00000585802.5:c.1126-169G= ENSP00000465598.1:n.1126-169G=
ENST00000587525.5:c.529-169G= ENSP00000467729.1:n.529-169G=
ENST00000593267.1:n.273-169G=
ENST00000614285.4:c.5086-169G= ENSP00000479983.1:n.5086-169G=
NM_000068.3:c.5086-169G= NP_000059.3:n.5086-169G=
NM_001127221.1:c.5071-169G= , LRG_7t1:c.5071-169G= NP_001120693.1:n.5071-169G=
NM_001127222.1:c.5068-169G= NP_001120694.1:n.5068-169G=
NM_001174080.1:c.5077-169G= NP_001167551.1:n.5077-169G=
NM_023035.2:c.5086-169G= NP_075461.2:n.5086-169G=
NM_000068.4:c.5086-169G= NP_000059.3:n.5086-169G=
NM_001127222.2:c.5068-169G= MANE Select NP_001120694.1:n.5068-169G=
NM_001174080.2:c.5077-169G= NP_001167551.1:n.5077-169G=
NM_023035.3:c.5086-169G= NP_075461.2:n.5086-169G=
NM_001127221.2:c.5071-169G= NP_001120693.1:n.5071-169G=