Canonical Allele Identifier: CA2455097

Gene: CACNA1D

Linked Data

• ClinVar Variation Id: 2801900
• ClinVar RCV Id: RCV003676393
• dbSNP Id: rs199874790
• ExAC: 3:53835340 G / A
• gnomAD v2: 3-53835340-G-A
• gnomAD v3: 3-53801313-G-A
• gnomAD v4: 3-53801313-G-A
• MyVariant Identifiers: chr3:g.53835340G>A (hg19) ; chr3:g.53801313G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801313G>A , CM000665.2:g.53801313G>A	GRCh38
NC_000003.11:g.53835340G>A , CM000665.1:g.53835340G>A	GRCh37
NC_000003.10:g.53810380G>A	NCBI36
NG_032999.1:g.311265G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5356G>A	ENSP00000418014.2:p.Ala1786Thr
ENST00000636633.2:n.2295G>A
ENST00000636999.2:n.731G>A
ENST00000288139.11:c.5356G>A MANE Plus Clinical	ENSP00000288139.3:p.Ala1786Thr
ENST00000350061.11:c.5296G>A MANE Select	ENSP00000288133.5:p.Ala1766Thr
ENST00000422281.7:c.5251G>A	ENSP00000409174.2:p.Ala1751Thr
ENST00000636448.1:c.1417G>A
ENST00000636570.1:c.5251G>A	ENSP00000490183.1:p.Ala1751Thr
ENST00000636629.1:n.652G>A
ENST00000636633.1:n.2295G>A
ENST00000636999.1:n.723G>A
ENST00000637424.1:c.5323G>A	ENSP00000489769.1:p.Ala1775Thr
ENST00000637844.1:n.50G>A
ENST00000288139.8:c.5356G>A	ENSP00000288139.3:p.Ala1786Thr
ENST00000350061.9:c.5296G>A	ENSP00000288133.5:p.Ala1766Thr
ENST00000422281.6:c.5251G>A	ENSP00000409174.2:p.Ala1751Thr
ENST00000481478.1:c.4375G>A	ENSP00000418014.1:p.Ala1459Thr
NM_000720.3:c.5356G>A	NP_000711.1:p.Ala1786Thr
NM_001128839.2:c.5251G>A	NP_001122311.1:p.Ala1751Thr
NM_001128840.2:c.5296G>A	NP_001122312.1:p.Ala1766Thr
XM_005265448.2:c.5251G>A	XP_005265505.1:p.Ala1751Thr
XM_011534094.1:c.5551G>A	XP_011532396.1:p.Ala1851Thr
XM_011534095.1:c.5440G>A	XP_011532397.1:p.Ala1814Thr
XM_011534096.1:c.5362G>A	XP_011532398.1:p.Ala1788Thr
XM_011534097.1:c.5014G>A	XP_011532399.1:p.Ala1672Thr
XM_011534098.1:c.5014G>A	XP_011532400.1:p.Ala1672Thr
XM_011534099.1:c.4639G>A	XP_011532401.1:p.Ala1547Thr
XM_011534100.1:c.5446G>A	XP_011532402.1:p.Ala1816Thr
XM_005265448.3:c.5251G>A	XP_005265505.1:p.Ala1751Thr
XM_011534094.2:c.5551G>A	XP_011532396.1:p.Ala1851Thr
XM_011534096.2:c.5362G>A	XP_011532398.1:p.Ala1788Thr
XM_011534097.2:c.5014G>A	XP_011532399.1:p.Ala1672Thr
XM_011534099.2:c.4639G>A	XP_011532401.1:p.Ala1547Thr
XM_011534100.2:c.5446G>A	XP_011532402.1:p.Ala1816Thr
XM_017007137.1:c.5551G>A	XP_016862626.1:p.Ala1851Thr
XM_017007138.1:c.5548G>A	XP_016862627.1:p.Ala1850Thr
XM_017007139.1:c.5551G>A	XP_016862628.1:p.Ala1851Thr
XM_017007140.1:c.5491G>A	XP_016862629.1:p.Ala1831Thr
XM_017007141.1:c.5491G>A	XP_016862630.1:p.Ala1831Thr
XM_017007142.1:c.5467G>A	XP_016862631.1:p.Ala1823Thr
XM_017007143.1:c.5467G>A	XP_016862632.1:p.Ala1823Thr
XM_017007144.1:c.5467G>A	XP_016862633.1:p.Ala1823Thr
XM_017007145.1:c.5422G>A	XP_016862634.1:p.Ala1808Thr
NM_001128840.3:c.5296G>A MANE Select	NP_001122312.1:p.Ala1766Thr
NM_000720.4:c.5356G>A MANE Plus Clinical	NP_000711.1:p.Ala1786Thr
NM_001128839.3:c.5251G>A	NP_001122311.1:p.Ala1751Thr