Canonical Allele Identifier: CA2582827079

Gene: CACNA1A

Linked Data

• gnomAD v4: 19-13261796-T-TGATA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13261796_13261797insGATA , CM000681.2:g.13261796_13261797insGATA	GRCh38
NC_000019.9:g.13372610_13372611insGATA , CM000681.1:g.13372610_13372611insGATA	GRCh37
NC_000019.8:g.13233610_13233611insGATA	NCBI36
NG_011569.1:g.249664_249665insTATC , LRG_7:g.249664_249665insTATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360228.11:c.4090-187_4090-186insTATC MANE Select	ENSP00000353362.5:n.4090-187_4090-186insTATC
ENST00000573710.7:c.4096-187_4096-186insTATC	ENSP00000460092.3:n.4096-187_4096-186insTATC
ENST00000590205.2:n.909_910insTATC
ENST00000635727.1:c.4093-187_4093-186insTATC	ENSP00000490001.1:n.4093-187_4093-186insTATC
ENST00000635742.1:n.79-187_79-186insTATC
ENST00000635895.1:c.4093-187_4093-186insTATC	ENSP00000490323.1:n.4093-187_4093-186insTATC
ENST00000635917.1:n.582-187_582-186insTATC
ENST00000636012.1:c.4093-187_4093-186insTATC	ENSP00000490223.1:n.4093-187_4093-186insTATC
ENST00000636389.1:c.4093-187_4093-186insTATC	ENSP00000489992.1:n.4093-187_4093-186insTATC
ENST00000636549.1:c.4093-187_4093-186insTATC	ENSP00000490578.1:n.4093-187_4093-186insTATC
ENST00000636816.1:n.778-187_778-186insTATC
ENST00000637004.1:n.556-187_556-186insTATC
ENST00000637276.1:c.4093-187_4093-186insTATC	ENSP00000489777.1:n.4093-187_4093-186insTATC
ENST00000637432.1:c.4102-187_4102-186insTATC	ENSP00000490617.1:n.4102-187_4102-186insTATC
ENST00000637692.1:n.412-187_412-186insTATC
ENST00000637736.1:c.3952-187_3952-186insTATC	ENSP00000489861.1:n.3952-187_3952-186insTATC
ENST00000637769.1:c.4093-187_4093-186insTATC	ENSP00000489778.1:n.4093-187_4093-186insTATC
ENST00000637927.1:c.4096-187_4096-186insTATC	ENSP00000489715.1:n.4096-187_4096-186insTATC
ENST00000638009.2:c.4093-187_4093-186insTATC	ENSP00000489913.1:n.4093-187_4093-186insTATC
ENST00000638029.1:c.4102-187_4102-186insTATC	ENSP00000489829.1:n.4102-187_4102-186insTATC
ENST00000664864.1:c.4288-187_4288-186insTATC	ENSP00000499449.1:n.4288-187_4288-186insTATC
ENST00000360228.9:c.4090-187_4090-186insTATC	ENSP00000353362.5:n.4090-187_4090-186insTATC
ENST00000573710.6:c.4093-187_4093-186insTATC	ENSP00000460092.2:n.4093-187_4093-186insTATC
ENST00000585802.5:c.148-187_148-186insTATC	ENSP00000465598.1:n.148-187_148-186insTATC
ENST00000590205.1:n.169-187_169-186insTATC
ENST00000614285.4:c.4102-187_4102-186insTATC	ENSP00000479983.1:n.4102-187_4102-186insTATC
NM_000068.3:c.4102-187_4102-186insTATC	NP_000059.3:n.4102-187_4102-186insTATC
NM_001127221.1:c.4093-187_4093-186insTATC , LRG_7t1:c.4093-187_4093-186insTATC	NP_001120693.1:n.4093-187_4093-186insTATC
NM_001127222.1:c.4090-187_4090-186insTATC	NP_001120694.1:n.4090-187_4090-186insTATC
NM_001174080.1:c.4093-187_4093-186insTATC	NP_001167551.1:n.4093-187_4093-186insTATC
NM_023035.2:c.4102-187_4102-186insTATC	NP_075461.2:n.4102-187_4102-186insTATC
NM_000068.4:c.4102-187_4102-186insTATC	NP_000059.3:n.4102-187_4102-186insTATC
NM_001127222.2:c.4090-187_4090-186insTATC MANE Select	NP_001120694.1:n.4090-187_4090-186insTATC
NM_001174080.2:c.4093-187_4093-186insTATC	NP_001167551.1:n.4093-187_4093-186insTATC
NM_023035.3:c.4102-187_4102-186insTATC	NP_075461.2:n.4102-187_4102-186insTATC
NM_001127221.2:c.4093-187_4093-186insTATC	NP_001120693.1:n.4093-187_4093-186insTATC