Canonical Allele Identifier: CA404347233
Gene: CACNA1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13359710C>G , CM000681.2:g.13359710C>G GRCh38
NC_000019.9:g.13470524C>G , CM000681.1:g.13470524C>G GRCh37
NC_000019.8:g.13331524C>G NCBI36
NG_011569.1:g.151751G>C , LRG_7:g.151751G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360228.11:c.874G>C MANE Select ENSP00000353362.5:p.Glu292Gln
ENST00000573710.7:c.874G>C ENSP00000460092.3:p.Glu292Gln
ENST00000593160.2:n.589G>C
ENST00000635727.1:c.874G>C ENSP00000490001.1:p.Glu292Gln
ENST00000635895.1:c.874G>C ENSP00000490323.1:p.Glu292Gln
ENST00000636012.1:c.874G>C ENSP00000490223.1:p.Glu292Gln
ENST00000636389.1:c.874G>C ENSP00000489992.1:p.Glu292Gln
ENST00000636549.1:c.874G>C ENSP00000490578.1:p.Glu292Gln
ENST00000636974.1:n.233G>C
ENST00000637276.1:c.874G>C ENSP00000489777.1:p.Glu292Gln
ENST00000637432.1:c.874G>C ENSP00000490617.1:p.Glu292Gln
ENST00000637736.1:c.733G>C ENSP00000489861.1:p.Glu245Gln
ENST00000637769.1:c.874G>C ENSP00000489778.1:p.Glu292Gln
ENST00000637927.1:c.874G>C ENSP00000489715.1:p.Glu292Gln
ENST00000637966.1:n.727G>C
ENST00000638009.2:c.874G>C ENSP00000489913.1:p.Glu292Gln
ENST00000638029.1:c.874G>C ENSP00000489829.1:p.Glu292Gln
ENST00000664864.1:c.1069G>C ENSP00000499449.1:p.Glu357Gln
ENST00000360228.9:c.874G>C ENSP00000353362.5:p.Glu292Gln
ENST00000573710.6:c.874G>C ENSP00000460092.2:p.Glu292Gln
ENST00000593160.1:n.94G>C
ENST00000614285.4:c.874G>C ENSP00000479983.1:p.Glu292Gln
NM_000068.3:c.874G>C NP_000059.3:p.Glu292Gln
NM_001127221.1:c.874G>C , LRG_7t1:c.874G>C NP_001120693.1:p.Glu292Gln
NM_001127222.1:c.874G>C NP_001120694.1:p.Glu292Gln
NM_001174080.1:c.874G>C NP_001167551.1:p.Glu292Gln
NM_023035.2:c.874G>C NP_075461.2:p.Glu292Gln
NM_000068.4:c.874G>C NP_000059.3:p.Glu292Gln
NM_001127222.2:c.874G>C MANE Select NP_001120694.1:p.Glu292Gln
NM_001174080.2:c.874G>C NP_001167551.1:p.Glu292Gln
NM_023035.3:c.874G>C NP_075461.2:p.Glu292Gln
NM_001127221.2:c.874G>C NP_001120693.1:p.Glu292Gln