Canonical Allele Identifier: CA353251535

Gene: CACNA1D

Linked Data

• ClinVar Variation Id: 1491291
• ClinVar RCV Id: RCV001986421
• dbSNP Id: rs2106780761
• gnomAD v4: 3-53801349-G-A
• MyVariant Identifiers: chr3:g.53835376G>A (hg19) ; chr3:g.53801349G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801349G>A , CM000665.2:g.53801349G>A	GRCh38
NC_000003.11:g.53835376G>A , CM000665.1:g.53835376G>A	GRCh37
NC_000003.10:g.53810416G>A	NCBI36
NG_032999.1:g.311301G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5392G>A	ENSP00000418014.2:p.Glu1798Lys
ENST00000636633.2:n.2331G>A
ENST00000636999.2:n.767G>A
ENST00000288139.11:c.5392G>A MANE Plus Clinical	ENSP00000288139.3:p.Glu1798Lys
ENST00000350061.11:c.5332G>A MANE Select	ENSP00000288133.5:p.Glu1778Lys
ENST00000422281.7:c.5287G>A	ENSP00000409174.2:p.Glu1763Lys
ENST00000636448.1:c.1453G>A
ENST00000636570.1:c.5287G>A	ENSP00000490183.1:p.Glu1763Lys
ENST00000636629.1:n.688G>A
ENST00000636633.1:n.2331G>A
ENST00000636999.1:n.759G>A
ENST00000637424.1:c.5359G>A	ENSP00000489769.1:p.Glu1787Lys
ENST00000637844.1:n.86G>A
ENST00000288139.8:c.5392G>A	ENSP00000288139.3:p.Glu1798Lys
ENST00000350061.9:c.5332G>A	ENSP00000288133.5:p.Glu1778Lys
ENST00000422281.6:c.5287G>A	ENSP00000409174.2:p.Glu1763Lys
ENST00000481478.1:c.4411G>A	ENSP00000418014.1:p.Glu1471Lys
NM_000720.3:c.5392G>A	NP_000711.1:p.Glu1798Lys
NM_001128839.2:c.5287G>A	NP_001122311.1:p.Glu1763Lys
NM_001128840.2:c.5332G>A	NP_001122312.1:p.Glu1778Lys
XM_005265448.2:c.5287G>A	XP_005265505.1:p.Glu1763Lys
XM_011534094.1:c.5587G>A	XP_011532396.1:p.Glu1863Lys
XM_011534095.1:c.5476G>A	XP_011532397.1:p.Glu1826Lys
XM_011534096.1:c.5398G>A	XP_011532398.1:p.Glu1800Lys
XM_011534097.1:c.5050G>A	XP_011532399.1:p.Glu1684Lys
XM_011534098.1:c.5050G>A	XP_011532400.1:p.Glu1684Lys
XM_011534099.1:c.4675G>A	XP_011532401.1:p.Glu1559Lys
XM_011534100.1:c.5482G>A	XP_011532402.1:p.Glu1828Lys
XM_005265448.3:c.5287G>A	XP_005265505.1:p.Glu1763Lys
XM_011534094.2:c.5587G>A	XP_011532396.1:p.Glu1863Lys
XM_011534096.2:c.5398G>A	XP_011532398.1:p.Glu1800Lys
XM_011534097.2:c.5050G>A	XP_011532399.1:p.Glu1684Lys
XM_011534099.2:c.4675G>A	XP_011532401.1:p.Glu1559Lys
XM_011534100.2:c.5482G>A	XP_011532402.1:p.Glu1828Lys
XM_017007137.1:c.5587G>A	XP_016862626.1:p.Glu1863Lys
XM_017007138.1:c.5584G>A	XP_016862627.1:p.Glu1862Lys
XM_017007139.1:c.5587G>A	XP_016862628.1:p.Glu1863Lys
XM_017007140.1:c.5527G>A	XP_016862629.1:p.Glu1843Lys
XM_017007141.1:c.5527G>A	XP_016862630.1:p.Glu1843Lys
XM_017007142.1:c.5503G>A	XP_016862631.1:p.Glu1835Lys
XM_017007143.1:c.5503G>A	XP_016862632.1:p.Glu1835Lys
XM_017007144.1:c.5503G>A	XP_016862633.1:p.Glu1835Lys
XM_017007145.1:c.5458G>A	XP_016862634.1:p.Glu1820Lys
NM_001128840.3:c.5332G>A MANE Select	NP_001122312.1:p.Glu1778Lys
NM_000720.4:c.5392G>A MANE Plus Clinical	NP_000711.1:p.Glu1798Lys
NM_001128839.3:c.5287G>A	NP_001122311.1:p.Glu1763Lys