Canonical Allele Identifier: CA631873953

Gene: CACNA1A

Linked Data

• dbSNP Id: rs372049268
• gnomAD v2: 19-13482464-G-A
• gnomAD v3: 19-13371650-G-A
• gnomAD v4: 19-13371650-G-A
• MyVariant Identifiers: chr19:g.13482464G>A (hg19) ; chr19:g.13482464_13482465delinsAT (hg19) ; chr19:g.13371650G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13371650G>A , CM000681.2:g.13371650G>A	GRCh38
NC_000019.9:g.13482464G>A , CM000681.1:g.13482464G>A	GRCh37
NC_000019.8:g.13343464G>A	NCBI36
NG_011569.1:g.139811C>T , LRG_7:g.139811C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360228.11:c.631+38C>T MANE Select	ENSP00000353362.5:n.631+38C>T
ENST00000573710.7:c.631+38C>T	ENSP00000460092.3:n.631+38C>T
ENST00000593160.2:n.346+38C>T
ENST00000635727.1:c.631+38C>T	ENSP00000490001.1:n.631+38C>T
ENST00000635895.1:c.631+38C>T	ENSP00000490323.1:n.631+38C>T
ENST00000636012.1:c.631+38C>T	ENSP00000490223.1:n.631+38C>T
ENST00000636389.1:c.631+38C>T	ENSP00000489992.1:n.631+38C>T
ENST00000636549.1:c.631+38C>T	ENSP00000490578.1:n.631+38C>T
ENST00000636966.1:n.519+38C>T
ENST00000637276.1:c.631+38C>T	ENSP00000489777.1:n.631+38C>T
ENST00000637432.1:c.631+38C>T	ENSP00000490617.1:n.631+38C>T
ENST00000637736.1:c.490+38C>T	ENSP00000489861.1:n.490+38C>T
ENST00000637769.1:c.631+38C>T	ENSP00000489778.1:n.631+38C>T
ENST00000637927.1:c.631+38C>T	ENSP00000489715.1:n.631+38C>T
ENST00000637966.1:n.484+38C>T
ENST00000637981.1:n.487C>T
ENST00000638009.2:c.631+38C>T	ENSP00000489913.1:n.631+38C>T
ENST00000638029.1:c.631+38C>T	ENSP00000489829.1:n.631+38C>T
ENST00000664864.1:c.826+38C>T	ENSP00000499449.1:n.826+38C>T
ENST00000360228.9:c.631+38C>T	ENSP00000353362.5:n.631+38C>T
ENST00000573710.6:c.631+38C>T	ENSP00000460092.2:n.631+38C>T
ENST00000614285.4:c.631+38C>T	ENSP00000479983.1:n.631+38C>T
NM_000068.3:c.631+38C>T	NP_000059.3:n.631+38C>T
NM_001127221.1:c.631+38C>T , LRG_7t1:c.631+38C>T	NP_001120693.1:n.631+38C>T
NM_001127222.1:c.631+38C>T	NP_001120694.1:n.631+38C>T
NM_001174080.1:c.631+38C>T	NP_001167551.1:n.631+38C>T
NM_023035.2:c.631+38C>T	NP_075461.2:n.631+38C>T
NM_000068.4:c.631+38C>T	NP_000059.3:n.631+38C>T
NM_001127222.2:c.631+38C>T MANE Select	NP_001120694.1:n.631+38C>T
NM_001174080.2:c.631+38C>T	NP_001167551.1:n.631+38C>T
NM_023035.3:c.631+38C>T	NP_075461.2:n.631+38C>T
NM_001127221.2:c.631+38C>T	NP_001120693.1:n.631+38C>T