Canonical Allele Identifier: CA404344422

Gene: CACNA1A

Linked Data

• MyVariant Identifiers: chr19:g.13414658C>A (hg19) ; chr19:g.13303844C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13303844C>A , CM000681.2:g.13303844C>A	GRCh38
NC_000019.9:g.13414658C>A , CM000681.1:g.13414658C>A	GRCh37
NC_000019.8:g.13275658C>A	NCBI36
NG_011569.1:g.207617G>T , LRG_7:g.207617G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360228.11:c.2027G>T MANE Select	ENSP00000353362.5:p.Gly676Val
ENST00000573710.7:c.2033G>T	ENSP00000460092.3:p.Gly678Val
ENST00000635727.1:c.2030G>T	ENSP00000490001.1:p.Gly677Val
ENST00000635895.1:c.2030G>T	ENSP00000490323.1:p.Gly677Val
ENST00000636012.1:c.2030G>T	ENSP00000490223.1:p.Gly677Val
ENST00000636389.1:c.2030G>T	ENSP00000489992.1:p.Gly677Val
ENST00000636549.1:c.2030G>T	ENSP00000490578.1:p.Gly677Val
ENST00000637276.1:c.2030G>T	ENSP00000489777.1:p.Gly677Val
ENST00000637432.1:c.2030G>T	ENSP00000490617.1:p.Gly677Val
ENST00000637736.1:c.1889G>T	ENSP00000489861.1:p.Gly630Val
ENST00000637769.1:c.2030G>T	ENSP00000489778.1:p.Gly677Val
ENST00000637927.1:c.2033G>T	ENSP00000489715.1:p.Gly678Val
ENST00000638009.2:c.2030G>T	ENSP00000489913.1:p.Gly677Val
ENST00000638029.1:c.2030G>T	ENSP00000489829.1:p.Gly677Val
ENST00000664864.1:c.2225G>T	ENSP00000499449.1:p.Gly742Val
ENST00000360228.9:c.2027G>T	ENSP00000353362.5:p.Gly676Val
ENST00000573710.6:c.2030G>T	ENSP00000460092.2:p.Gly677Val
ENST00000614285.4:c.2030G>T	ENSP00000479983.1:p.Gly677Val
NM_000068.3:c.2030G>T	NP_000059.3:p.Gly677Val
NM_001127221.1:c.2030G>T , LRG_7t1:c.2030G>T	NP_001120693.1:p.Gly677Val
NM_001127222.1:c.2027G>T	NP_001120694.1:p.Gly676Val
NM_001174080.1:c.2030G>T	NP_001167551.1:p.Gly677Val
NM_023035.2:c.2030G>T	NP_075461.2:p.Gly677Val
NM_000068.4:c.2030G>T	NP_000059.3:p.Gly677Val
NM_001127222.2:c.2027G>T MANE Select	NP_001120694.1:p.Gly676Val
NM_001174080.2:c.2030G>T	NP_001167551.1:p.Gly677Val
NM_023035.3:c.2030G>T	NP_075461.2:p.Gly677Val
NM_001127221.2:c.2030G>T	NP_001120693.1:p.Gly677Val