Canonical Allele Identifier: CA2582827075

Gene: CACNA1A

Linked Data

• gnomAD v4: 19-13261794-AAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13261795_13261796del , CM000681.2:g.13261795_13261796del	GRCh38
NC_000019.9:g.13372609_13372610del , CM000681.1:g.13372609_13372610del	GRCh37
NC_000019.8:g.13233609_13233610del	NCBI36
NG_011569.1:g.249665_249666del , LRG_7:g.249665_249666del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360228.11:c.4090-186_4090-185del MANE Select	ENSP00000353362.5:n.4090-186_4090-185del
ENST00000573710.7:c.4096-186_4096-185del	ENSP00000460092.3:n.4096-186_4096-185del
ENST00000590205.2:n.910_911del
ENST00000635727.1:c.4093-186_4093-185del	ENSP00000490001.1:n.4093-186_4093-185del
ENST00000635742.1:n.79-186_79-185del
ENST00000635895.1:c.4093-186_4093-185del	ENSP00000490323.1:n.4093-186_4093-185del
ENST00000635917.1:n.582-186_582-185del
ENST00000636012.1:c.4093-186_4093-185del	ENSP00000490223.1:n.4093-186_4093-185del
ENST00000636389.1:c.4093-186_4093-185del	ENSP00000489992.1:n.4093-186_4093-185del
ENST00000636549.1:c.4093-186_4093-185del	ENSP00000490578.1:n.4093-186_4093-185del
ENST00000636816.1:n.778-186_778-185del
ENST00000637004.1:n.556-186_556-185del
ENST00000637276.1:c.4093-186_4093-185del	ENSP00000489777.1:n.4093-186_4093-185del
ENST00000637432.1:c.4102-186_4102-185del	ENSP00000490617.1:n.4102-186_4102-185del
ENST00000637692.1:n.412-186_412-185del
ENST00000637736.1:c.3952-186_3952-185del	ENSP00000489861.1:n.3952-186_3952-185del
ENST00000637769.1:c.4093-186_4093-185del	ENSP00000489778.1:n.4093-186_4093-185del
ENST00000637927.1:c.4096-186_4096-185del	ENSP00000489715.1:n.4096-186_4096-185del
ENST00000638009.2:c.4093-186_4093-185del	ENSP00000489913.1:n.4093-186_4093-185del
ENST00000638029.1:c.4102-186_4102-185del	ENSP00000489829.1:n.4102-186_4102-185del
ENST00000664864.1:c.4288-186_4288-185del	ENSP00000499449.1:n.4288-186_4288-185del
ENST00000360228.9:c.4090-186_4090-185del	ENSP00000353362.5:n.4090-186_4090-185del
ENST00000573710.6:c.4093-186_4093-185del	ENSP00000460092.2:n.4093-186_4093-185del
ENST00000585802.5:c.148-186_148-185del	ENSP00000465598.1:n.148-186_148-185del
ENST00000590205.1:n.169-186_169-185del
ENST00000614285.4:c.4102-186_4102-185del	ENSP00000479983.1:n.4102-186_4102-185del
NM_000068.3:c.4102-186_4102-185del	NP_000059.3:n.4102-186_4102-185del
NM_001127221.1:c.4093-186_4093-185del , LRG_7t1:c.4093-186_4093-185del	NP_001120693.1:n.4093-186_4093-185del
NM_001127222.1:c.4090-186_4090-185del	NP_001120694.1:n.4090-186_4090-185del
NM_001174080.1:c.4093-186_4093-185del	NP_001167551.1:n.4093-186_4093-185del
NM_023035.2:c.4102-186_4102-185del	NP_075461.2:n.4102-186_4102-185del
NM_000068.4:c.4102-186_4102-185del	NP_000059.3:n.4102-186_4102-185del
NM_001127222.2:c.4090-186_4090-185del MANE Select	NP_001120694.1:n.4090-186_4090-185del
NM_001174080.2:c.4093-186_4093-185del	NP_001167551.1:n.4093-186_4093-185del
NM_023035.3:c.4102-186_4102-185del	NP_075461.2:n.4102-186_4102-185del
NM_001127221.2:c.4093-186_4093-185del	NP_001120693.1:n.4093-186_4093-185del