Canonical Allele Identifier: CA2740091966

Gene: CACNA1A

Linked Data

• ClinVar Variation Id: 2953327
• ClinVar RCV Id: RCV003810445

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13506049_13506051del , CM000681.2:g.13506049_13506051del	GRCh38
NC_000019.9:g.13616863_13616865del , CM000681.1:g.13616863_13616865del	GRCh37
NC_000019.8:g.13477863_13477865del	NCBI36
NG_011569.1:g.5410_5412del , LRG_7:g.5410_5412del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360228.11:c.174_176del MANE Select	ENSP00000353362.5:p.Met59del
ENST00000573710.7:c.174_176del	ENSP00000460092.3:p.Met59del
ENST00000574974.3:c.195-50862_195-50860del	ENSP00000459963.2:n.195-50862_195-50860del
ENST00000635727.1:c.174_176del	ENSP00000490001.1:p.Met59del
ENST00000635895.1:c.174_176del	ENSP00000490323.1:p.Met59del
ENST00000636012.1:c.174_176del	ENSP00000490223.1:p.Met59del
ENST00000636389.1:c.174_176del	ENSP00000489992.1:p.Met59del
ENST00000636549.1:c.174_176del	ENSP00000490578.1:p.Met59del
ENST00000636966.1:n.62_64del
ENST00000637276.1:c.174_176del	ENSP00000489777.1:p.Met59del
ENST00000637432.1:c.174_176del	ENSP00000490617.1:p.Met59del
ENST00000637616.1:n.182_184del
ENST00000637736.1:c.174_176del	ENSP00000489861.1:p.Met59del
ENST00000637769.1:c.174_176del	ENSP00000489778.1:p.Met59del
ENST00000637927.1:c.174_176del	ENSP00000489715.1:p.Met59del
ENST00000637966.1:n.27_29del
ENST00000638009.2:c.174_176del	ENSP00000489913.1:p.Met59del
ENST00000638029.1:c.174_176del	ENSP00000489829.1:p.Met59del
ENST00000664864.1:c.369_371del	ENSP00000499449.1:p.Met124del
ENST00000360228.9:c.174_176del	ENSP00000353362.5:p.Met59del
ENST00000573710.6:c.174_176del	ENSP00000460092.2:p.Met59del
ENST00000574974.1:c.68-50862_68-50860del	ENSP00000459963.1:n.68-50862_68-50860del
ENST00000614285.4:c.174_176del	ENSP00000479983.1:p.Met59del
NM_000068.3:c.174_176del	NP_000059.3:p.Met59del
NM_001127221.1:c.174_176del , LRG_7t1:c.174_176del	NP_001120693.1:p.Met59del
NM_001127222.1:c.174_176del	NP_001120694.1:p.Met59del
NM_001174080.1:c.174_176del	NP_001167551.1:p.Met59del
NM_023035.2:c.174_176del	NP_075461.2:p.Met59del
NM_000068.4:c.174_176del	NP_000059.3:p.Met59del
NM_001127222.2:c.174_176del MANE Select	NP_001120694.1:p.Met59del
NM_001174080.2:c.174_176del	NP_001167551.1:p.Met59del
NM_023035.3:c.174_176del	NP_075461.2:p.Met59del
NM_001127221.2:c.174_176del	NP_001120693.1:p.Met59del