Canonical Allele Identifier: CA433895861

Gene: CACNA1D

Linked Data

• MyVariant Identifiers: chr3:g.53835165C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801138C>A , CM000665.2:g.53801138C>A	GRCh38
NC_000003.11:g.53835165C>A , CM000665.1:g.53835165C>A	GRCh37
NC_000003.10:g.53810205C>A	NCBI36
NG_032999.1:g.311090C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5181C>A	ENSP00000418014.2:p.Thr1727=
ENST00000636633.2:n.2194-74C>A
ENST00000636999.2:n.556C>A
ENST00000288139.11:c.5181C>A MANE Plus Clinical	ENSP00000288139.3:p.Thr1727=
ENST00000350061.11:c.5121C>A MANE Select	ENSP00000288133.5:p.Thr1707=
ENST00000422281.7:c.5076C>A	ENSP00000409174.2:p.Thr1692=
ENST00000636448.1:c.1316-74C>A
ENST00000636570.1:c.5076C>A	ENSP00000490183.1:p.Thr1692=
ENST00000636629.1:n.477C>A
ENST00000636633.1:n.2194-74C>A
ENST00000636999.1:n.548C>A
ENST00000637424.1:c.5148C>A	ENSP00000489769.1:p.Thr1716=
ENST00000288139.8:c.5181C>A	ENSP00000288139.3:p.Thr1727=
ENST00000350061.9:c.5121C>A	ENSP00000288133.5:p.Thr1707=
ENST00000422281.6:c.5076C>A	ENSP00000409174.2:p.Thr1692=
ENST00000481478.1:c.4200C>A	ENSP00000418014.1:p.Thr1400=
NM_000720.3:c.5181C>A	NP_000711.1:p.Thr1727=
NM_001128839.2:c.5076C>A	NP_001122311.1:p.Thr1692=
NM_001128840.2:c.5121C>A	NP_001122312.1:p.Thr1707=
XM_005265448.2:c.5076C>A	XP_005265505.1:p.Thr1692=
XM_011534094.1:c.5376C>A	XP_011532396.1:p.Thr1792=
XM_011534095.1:c.5265C>A	XP_011532397.1:p.Thr1755=
XM_011534096.1:c.5187C>A	XP_011532398.1:p.Thr1729=
XM_011534097.1:c.4839C>A	XP_011532399.1:p.Thr1613=
XM_011534098.1:c.4839C>A	XP_011532400.1:p.Thr1613=
XM_011534099.1:c.4464C>A	XP_011532401.1:p.Thr1488=
XM_011534100.1:c.5271C>A	XP_011532402.1:p.Thr1757=
XM_005265448.3:c.5076C>A	XP_005265505.1:p.Thr1692=
XM_011534094.2:c.5376C>A	XP_011532396.1:p.Thr1792=
XM_011534096.2:c.5187C>A	XP_011532398.1:p.Thr1729=
XM_011534097.2:c.4839C>A	XP_011532399.1:p.Thr1613=
XM_011534099.2:c.4464C>A	XP_011532401.1:p.Thr1488=
XM_011534100.2:c.5271C>A	XP_011532402.1:p.Thr1757=
XM_017007137.1:c.5376C>A	XP_016862626.1:p.Thr1792=
XM_017007138.1:c.5373C>A	XP_016862627.1:p.Thr1791=
XM_017007139.1:c.5376C>A	XP_016862628.1:p.Thr1792=
XM_017007140.1:c.5316C>A	XP_016862629.1:p.Thr1772=
XM_017007141.1:c.5316C>A	XP_016862630.1:p.Thr1772=
XM_017007142.1:c.5292C>A	XP_016862631.1:p.Thr1764=
XM_017007143.1:c.5292C>A	XP_016862632.1:p.Thr1764=
XM_017007144.1:c.5292C>A	XP_016862633.1:p.Thr1764=
XM_017007145.1:c.5247C>A	XP_016862634.1:p.Thr1749=
NM_001128840.3:c.5121C>A MANE Select	NP_001122312.1:p.Thr1707=
NM_000720.4:c.5181C>A MANE Plus Clinical	NP_000711.1:p.Thr1727=
NM_001128839.3:c.5076C>A	NP_001122311.1:p.Thr1692=