Canonical Allele Identifier: CA305546466

Gene: CACNA1A

Linked Data

• dbSNP Id: rs536329977
• gnomAD v2: 19-13373398-T-TAGA
• gnomAD v3: 19-13262584-T-TAGA
• gnomAD v4: 19-13262584-T-TAGA
• MyVariant Identifiers: chr19:g.13373398_13373399insAGA (hg19) ; chr19:g.13262584_13262585insAGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13262584_13262585insAGA , CM000681.2:g.13262584_13262585insAGA	GRCh38
NC_000019.9:g.13373398_13373399insAGA , CM000681.1:g.13373398_13373399insAGA	GRCh37
NC_000019.8:g.13234398_13234399insAGA	NCBI36
NG_011569.1:g.248876_248877insTCT , LRG_7:g.248876_248877insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360228.11:c.4089+149_4089+150insTCT MANE Select	ENSP00000353362.5:n.4089+149_4089+150insTCT
ENST00000573710.7:c.4095+149_4095+150insTCT	ENSP00000460092.3:n.4095+149_4095+150insTCT
ENST00000590205.2:n.121_122insTCT
ENST00000635727.1:c.4092+149_4092+150insTCT	ENSP00000490001.1:n.4092+149_4092+150insTCT
ENST00000635742.1:n.78+149_78+150insTCT
ENST00000635895.1:c.4092+149_4092+150insTCT	ENSP00000490323.1:n.4092+149_4092+150insTCT
ENST00000635917.1:n.581+149_581+150insTCT
ENST00000636012.1:c.4092+149_4092+150insTCT	ENSP00000490223.1:n.4092+149_4092+150insTCT
ENST00000636389.1:c.4092+149_4092+150insTCT	ENSP00000489992.1:n.4092+149_4092+150insTCT
ENST00000636549.1:c.4092+149_4092+150insTCT	ENSP00000490578.1:n.4092+149_4092+150insTCT
ENST00000636816.1:n.777+149_777+150insTCT
ENST00000637004.1:n.555+149_555+150insTCT
ENST00000637276.1:c.4092+149_4092+150insTCT	ENSP00000489777.1:n.4092+149_4092+150insTCT
ENST00000637432.1:c.4101+149_4101+150insTCT	ENSP00000490617.1:n.4101+149_4101+150insTCT
ENST00000637692.1:n.411+149_411+150insTCT
ENST00000637736.1:c.3951+149_3951+150insTCT	ENSP00000489861.1:n.3951+149_3951+150insTCT
ENST00000637769.1:c.4092+149_4092+150insTCT	ENSP00000489778.1:n.4092+149_4092+150insTCT
ENST00000637927.1:c.4095+149_4095+150insTCT	ENSP00000489715.1:n.4095+149_4095+150insTCT
ENST00000638009.2:c.4092+149_4092+150insTCT	ENSP00000489913.1:n.4092+149_4092+150insTCT
ENST00000638029.1:c.4101+149_4101+150insTCT	ENSP00000489829.1:n.4101+149_4101+150insTCT
ENST00000664864.1:c.4287+149_4287+150insTCT	ENSP00000499449.1:n.4287+149_4287+150insTCT
ENST00000360228.9:c.4089+149_4089+150insTCT	ENSP00000353362.5:n.4089+149_4089+150insTCT
ENST00000573710.6:c.4092+149_4092+150insTCT	ENSP00000460092.2:n.4092+149_4092+150insTCT
ENST00000585802.5:c.147+149_147+150insTCT	ENSP00000465598.1:n.147+149_147+150insTCT
ENST00000590205.1:n.168+149_168+150insTCT
ENST00000614285.4:c.4101+149_4101+150insTCT	ENSP00000479983.1:n.4101+149_4101+150insTCT
NM_000068.3:c.4101+149_4101+150insTCT	NP_000059.3:n.4101+149_4101+150insTCT
NM_001127221.1:c.4092+149_4092+150insTCT , LRG_7t1:c.4092+149_4092+150insTCT	NP_001120693.1:n.4092+149_4092+150insTCT
NM_001127222.1:c.4089+149_4089+150insTCT	NP_001120694.1:n.4089+149_4089+150insTCT
NM_001174080.1:c.4092+149_4092+150insTCT	NP_001167551.1:n.4092+149_4092+150insTCT
NM_023035.2:c.4101+149_4101+150insTCT	NP_075461.2:n.4101+149_4101+150insTCT
NM_000068.4:c.4101+149_4101+150insTCT	NP_000059.3:n.4101+149_4101+150insTCT
NM_001127222.2:c.4089+149_4089+150insTCT MANE Select	NP_001120694.1:n.4089+149_4089+150insTCT
NM_001174080.2:c.4092+149_4092+150insTCT	NP_001167551.1:n.4092+149_4092+150insTCT
NM_023035.3:c.4101+149_4101+150insTCT	NP_075461.2:n.4101+149_4101+150insTCT
NM_001127221.2:c.4092+149_4092+150insTCT	NP_001120693.1:n.4092+149_4092+150insTCT