Canonical Allele Identifier: CA404340107

Gene: CACNA1A

Linked Data

• MyVariant Identifiers: chr19:g.13373642T>G (hg19) ; chr19:g.13262828T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13262828T>G , CM000681.2:g.13262828T>G	GRCh38
NC_000019.9:g.13373642T>G , CM000681.1:g.13373642T>G	GRCh37
NC_000019.8:g.13234642T>G	NCBI36
NG_011569.1:g.248633A>C , LRG_7:g.248633A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360228.11:c.3995A>C MANE Select	ENSP00000353362.5:p.Asn1332Thr
ENST00000573710.7:c.4001A>C	ENSP00000460092.3:p.Asn1334Thr
ENST00000635727.1:c.3998A>C	ENSP00000490001.1:p.Asn1333Thr
ENST00000635895.1:c.3998A>C	ENSP00000490323.1:p.Asn1333Thr
ENST00000635917.1:n.487A>C
ENST00000636012.1:c.3998A>C	ENSP00000490223.1:p.Asn1333Thr
ENST00000636389.1:c.3998A>C	ENSP00000489992.1:p.Asn1333Thr
ENST00000636549.1:c.3998A>C	ENSP00000490578.1:p.Asn1333Thr
ENST00000636816.1:n.683A>C
ENST00000637004.1:n.461A>C
ENST00000637276.1:c.3998A>C	ENSP00000489777.1:p.Asn1333Thr
ENST00000637432.1:c.4007A>C	ENSP00000490617.1:p.Asn1336Thr
ENST00000637692.1:n.317A>C
ENST00000637736.1:c.3857A>C	ENSP00000489861.1:p.Asn1286Thr
ENST00000637769.1:c.3998A>C	ENSP00000489778.1:p.Asn1333Thr
ENST00000637927.1:c.4001A>C	ENSP00000489715.1:p.Asn1334Thr
ENST00000638009.2:c.3998A>C	ENSP00000489913.1:p.Asn1333Thr
ENST00000638029.1:c.4007A>C	ENSP00000489829.1:p.Asn1336Thr
ENST00000664864.1:c.4193A>C	ENSP00000499449.1:p.Asn1398Thr
ENST00000360228.9:c.3995A>C	ENSP00000353362.5:p.Asn1332Thr
ENST00000573710.6:c.3998A>C	ENSP00000460092.2:p.Asn1333Thr
ENST00000585802.5:c.53A>C	ENSP00000465598.1:p.Asn18Thr
ENST00000590205.1:n.74A>C
ENST00000614285.4:c.4007A>C	ENSP00000479983.1:p.Asn1336Thr
NM_000068.3:c.4007A>C	NP_000059.3:p.Asn1336Thr
NM_001127221.1:c.3998A>C , LRG_7t1:c.3998A>C	NP_001120693.1:p.Asn1333Thr
NM_001127222.1:c.3995A>C	NP_001120694.1:p.Asn1332Thr
NM_001174080.1:c.3998A>C	NP_001167551.1:p.Asn1333Thr
NM_023035.2:c.4007A>C	NP_075461.2:p.Asn1336Thr
NM_000068.4:c.4007A>C	NP_000059.3:p.Asn1336Thr
NM_001127222.2:c.3995A>C MANE Select	NP_001120694.1:p.Asn1332Thr
NM_001174080.2:c.3998A>C	NP_001167551.1:p.Asn1333Thr
NM_023035.3:c.4007A>C	NP_075461.2:p.Asn1336Thr
NM_001127221.2:c.3998A>C	NP_001120693.1:p.Asn1333Thr