Canonical Allele Identifier: CA2813672106

Gene: CACNA1A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13262722_13262723insAC , CM000681.2:g.13262722_13262723insAC	GRCh38
NC_000019.9:g.13373536_13373537insAC , CM000681.1:g.13373536_13373537insAC	GRCh37
NC_000019.8:g.13234536_13234537insAC	NCBI36
NG_011569.1:g.248738_248739insGT , LRG_7:g.248738_248739insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360228.11:c.4089+11_4089+12insGT MANE Select	ENSP00000353362.5:n.4089+11_4089+12insGT
ENST00000573710.7:c.4095+11_4095+12insGT	ENSP00000460092.3:n.4095+11_4095+12insGT
ENST00000635727.1:c.4092+11_4092+12insGT	ENSP00000490001.1:n.4092+11_4092+12insGT
ENST00000635742.1:n.78+11_78+12insGT
ENST00000635895.1:c.4092+11_4092+12insGT	ENSP00000490323.1:n.4092+11_4092+12insGT
ENST00000635917.1:n.581+11_581+12insGT
ENST00000636012.1:c.4092+11_4092+12insGT	ENSP00000490223.1:n.4092+11_4092+12insGT
ENST00000636389.1:c.4092+11_4092+12insGT	ENSP00000489992.1:n.4092+11_4092+12insGT
ENST00000636549.1:c.4092+11_4092+12insGT	ENSP00000490578.1:n.4092+11_4092+12insGT
ENST00000636816.1:n.777+11_777+12insGT
ENST00000637004.1:n.555+11_555+12insGT
ENST00000637276.1:c.4092+11_4092+12insGT	ENSP00000489777.1:n.4092+11_4092+12insGT
ENST00000637432.1:c.4101+11_4101+12insGT	ENSP00000490617.1:n.4101+11_4101+12insGT
ENST00000637692.1:n.411+11_411+12insGT
ENST00000637736.1:c.3951+11_3951+12insGT	ENSP00000489861.1:n.3951+11_3951+12insGT
ENST00000637769.1:c.4092+11_4092+12insGT	ENSP00000489778.1:n.4092+11_4092+12insGT
ENST00000637927.1:c.4095+11_4095+12insGT	ENSP00000489715.1:n.4095+11_4095+12insGT
ENST00000638009.2:c.4092+11_4092+12insGT	ENSP00000489913.1:n.4092+11_4092+12insGT
ENST00000638029.1:c.4101+11_4101+12insGT	ENSP00000489829.1:n.4101+11_4101+12insGT
ENST00000664864.1:c.4287+11_4287+12insGT	ENSP00000499449.1:n.4287+11_4287+12insGT
ENST00000360228.9:c.4089+11_4089+12insGT	ENSP00000353362.5:n.4089+11_4089+12insGT
ENST00000573710.6:c.4092+11_4092+12insGT	ENSP00000460092.2:n.4092+11_4092+12insGT
ENST00000585802.5:c.147+11_147+12insGT	ENSP00000465598.1:n.147+11_147+12insGT
ENST00000590205.1:n.168+11_168+12insGT
ENST00000614285.4:c.4101+11_4101+12insGT	ENSP00000479983.1:n.4101+11_4101+12insGT
NM_000068.3:c.4101+11_4101+12insGT	NP_000059.3:n.4101+11_4101+12insGT
NM_001127221.1:c.4092+11_4092+12insGT , LRG_7t1:c.4092+11_4092+12insGT	NP_001120693.1:n.4092+11_4092+12insGT
NM_001127222.1:c.4089+11_4089+12insGT	NP_001120694.1:n.4089+11_4089+12insGT
NM_001174080.1:c.4092+11_4092+12insGT	NP_001167551.1:n.4092+11_4092+12insGT
NM_023035.2:c.4101+11_4101+12insGT	NP_075461.2:n.4101+11_4101+12insGT
NM_000068.4:c.4101+11_4101+12insGT	NP_000059.3:n.4101+11_4101+12insGT
NM_001127222.2:c.4089+11_4089+12insGT MANE Select	NP_001120694.1:n.4089+11_4089+12insGT
NM_001174080.2:c.4092+11_4092+12insGT	NP_001167551.1:n.4092+11_4092+12insGT
NM_023035.3:c.4101+11_4101+12insGT	NP_075461.2:n.4101+11_4101+12insGT
NM_001127221.2:c.4092+11_4092+12insGT	NP_001120693.1:n.4092+11_4092+12insGT