Canonical Allele Identifier: CA2582826801

Gene: CACNA1A

Linked Data

• gnomAD v4: 19-13261366-GCCCAAGTGGCCAATGCCTCTAGCCACTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13261370_13261397del , CM000681.2:g.13261370_13261397del	GRCh38
NC_000019.9:g.13372184_13372211del , CM000681.1:g.13372184_13372211del	GRCh37
NC_000019.8:g.13233184_13233211del	NCBI36
NG_011569.1:g.250067_250094del , LRG_7:g.250067_250094del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360228.11:c.4250+56_4250+83del MANE Select	ENSP00000353362.5:n.4250+56_4250+83del
ENST00000573710.7:c.4256+56_4256+83del	ENSP00000460092.3:n.4256+56_4256+83del
ENST00000590205.2:n.1312_1339del
ENST00000635727.1:c.4253+56_4253+83del	ENSP00000490001.1:n.4253+56_4253+83del
ENST00000635742.1:n.239+56_239+83del
ENST00000635895.1:c.4253+56_4253+83del	ENSP00000490323.1:n.4253+56_4253+83del
ENST00000635917.1:n.742+56_742+83del
ENST00000636012.1:c.4253+56_4253+83del	ENSP00000490223.1:n.4253+56_4253+83del
ENST00000636389.1:c.4253+56_4253+83del	ENSP00000489992.1:n.4253+56_4253+83del
ENST00000636549.1:c.4253+56_4253+83del	ENSP00000490578.1:n.4253+56_4253+83del
ENST00000636816.1:n.938+56_938+83del
ENST00000637004.1:n.716+56_716+83del
ENST00000637276.1:c.4253+56_4253+83del	ENSP00000489777.1:n.4253+56_4253+83del
ENST00000637432.1:c.4262+56_4262+83del	ENSP00000490617.1:n.4262+56_4262+83del
ENST00000637692.1:n.572+56_572+83del
ENST00000637736.1:c.4112+56_4112+83del	ENSP00000489861.1:n.4112+56_4112+83del
ENST00000637769.1:c.4253+56_4253+83del	ENSP00000489778.1:n.4253+56_4253+83del
ENST00000637927.1:c.4256+56_4256+83del	ENSP00000489715.1:n.4256+56_4256+83del
ENST00000638009.2:c.4253+56_4253+83del	ENSP00000489913.1:n.4253+56_4253+83del
ENST00000638029.1:c.4262+56_4262+83del	ENSP00000489829.1:n.4262+56_4262+83del
ENST00000664864.1:c.4448+56_4448+83del	ENSP00000499449.1:n.4448+56_4448+83del
ENST00000360228.9:c.4250+56_4250+83del	ENSP00000353362.5:n.4250+56_4250+83del
ENST00000573710.6:c.4253+56_4253+83del	ENSP00000460092.2:n.4253+56_4253+83del
ENST00000585802.5:c.308+56_308+83del	ENSP00000465598.1:n.308+56_308+83del
ENST00000614285.4:c.4262+56_4262+83del	ENSP00000479983.1:n.4262+56_4262+83del
NM_000068.3:c.4262+56_4262+83del	NP_000059.3:n.4262+56_4262+83del
NM_001127221.1:c.4253+56_4253+83del , LRG_7t1:c.4253+56_4253+83del	NP_001120693.1:n.4253+56_4253+83del
NM_001127222.1:c.4250+56_4250+83del	NP_001120694.1:n.4250+56_4250+83del
NM_001174080.1:c.4253+56_4253+83del	NP_001167551.1:n.4253+56_4253+83del
NM_023035.2:c.4262+56_4262+83del	NP_075461.2:n.4262+56_4262+83del
NM_000068.4:c.4262+56_4262+83del	NP_000059.3:n.4262+56_4262+83del
NM_001127222.2:c.4250+56_4250+83del MANE Select	NP_001120694.1:n.4250+56_4250+83del
NM_001174080.2:c.4253+56_4253+83del	NP_001167551.1:n.4253+56_4253+83del
NM_023035.3:c.4262+56_4262+83del	NP_075461.2:n.4262+56_4262+83del
NM_001127221.2:c.4253+56_4253+83del	NP_001120693.1:n.4253+56_4253+83del