Canonical Allele Identifier: CA2813672104

Gene: CACNA1A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13262704_13262718del , CM000681.2:g.13262704_13262718del	GRCh38
NC_000019.9:g.13373518_13373532del , CM000681.1:g.13373518_13373532del	GRCh37
NC_000019.8:g.13234518_13234532del	NCBI36
NG_011569.1:g.248745_248759del , LRG_7:g.248745_248759del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360228.11:c.4089+18_4089+32del MANE Select	ENSP00000353362.5:n.4089+18_4089+32del
ENST00000573710.7:c.4095+18_4095+32del	ENSP00000460092.3:n.4095+18_4095+32del
ENST00000635727.1:c.4092+18_4092+32del	ENSP00000490001.1:n.4092+18_4092+32del
ENST00000635742.1:n.78+18_78+32del
ENST00000635895.1:c.4092+18_4092+32del	ENSP00000490323.1:n.4092+18_4092+32del
ENST00000635917.1:n.581+18_581+32del
ENST00000636012.1:c.4092+18_4092+32del	ENSP00000490223.1:n.4092+18_4092+32del
ENST00000636389.1:c.4092+18_4092+32del	ENSP00000489992.1:n.4092+18_4092+32del
ENST00000636549.1:c.4092+18_4092+32del	ENSP00000490578.1:n.4092+18_4092+32del
ENST00000636816.1:n.777+18_777+32del
ENST00000637004.1:n.555+18_555+32del
ENST00000637276.1:c.4092+18_4092+32del	ENSP00000489777.1:n.4092+18_4092+32del
ENST00000637432.1:c.4101+18_4101+32del	ENSP00000490617.1:n.4101+18_4101+32del
ENST00000637692.1:n.411+18_411+32del
ENST00000637736.1:c.3951+18_3951+32del	ENSP00000489861.1:n.3951+18_3951+32del
ENST00000637769.1:c.4092+18_4092+32del	ENSP00000489778.1:n.4092+18_4092+32del
ENST00000637927.1:c.4095+18_4095+32del	ENSP00000489715.1:n.4095+18_4095+32del
ENST00000638009.2:c.4092+18_4092+32del	ENSP00000489913.1:n.4092+18_4092+32del
ENST00000638029.1:c.4101+18_4101+32del	ENSP00000489829.1:n.4101+18_4101+32del
ENST00000664864.1:c.4287+18_4287+32del	ENSP00000499449.1:n.4287+18_4287+32del
ENST00000360228.9:c.4089+18_4089+32del	ENSP00000353362.5:n.4089+18_4089+32del
ENST00000573710.6:c.4092+18_4092+32del	ENSP00000460092.2:n.4092+18_4092+32del
ENST00000585802.5:c.147+18_147+32del	ENSP00000465598.1:n.147+18_147+32del
ENST00000590205.1:n.168+18_168+32del
ENST00000614285.4:c.4101+18_4101+32del	ENSP00000479983.1:n.4101+18_4101+32del
NM_000068.3:c.4101+18_4101+32del	NP_000059.3:n.4101+18_4101+32del
NM_001127221.1:c.4092+18_4092+32del , LRG_7t1:c.4092+18_4092+32del	NP_001120693.1:n.4092+18_4092+32del
NM_001127222.1:c.4089+18_4089+32del	NP_001120694.1:n.4089+18_4089+32del
NM_001174080.1:c.4092+18_4092+32del	NP_001167551.1:n.4092+18_4092+32del
NM_023035.2:c.4101+18_4101+32del	NP_075461.2:n.4101+18_4101+32del
NM_000068.4:c.4101+18_4101+32del	NP_000059.3:n.4101+18_4101+32del
NM_001127222.2:c.4089+18_4089+32del MANE Select	NP_001120694.1:n.4089+18_4089+32del
NM_001174080.2:c.4092+18_4092+32del	NP_001167551.1:n.4092+18_4092+32del
NM_023035.3:c.4101+18_4101+32del	NP_075461.2:n.4101+18_4101+32del
NM_001127221.2:c.4092+18_4092+32del	NP_001120693.1:n.4092+18_4092+32del