Canonical Allele Identifier: CA433895912

Gene: CACNA1D

Linked Data

• MyVariant Identifiers: chr3:g.53835187A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801160A>C , CM000665.2:g.53801160A>C	GRCh38
NC_000003.11:g.53835187A>C , CM000665.1:g.53835187A>C	GRCh37
NC_000003.10:g.53810227A>C	NCBI36
NG_032999.1:g.311112A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5203A>C	ENSP00000418014.2:p.Arg1735=
ENST00000636633.2:n.2194-52A>C
ENST00000636999.2:n.578A>C
ENST00000288139.11:c.5203A>C MANE Plus Clinical	ENSP00000288139.3:p.Arg1735=
ENST00000350061.11:c.5143A>C MANE Select	ENSP00000288133.5:p.Arg1715=
ENST00000422281.7:c.5098A>C	ENSP00000409174.2:p.Arg1700=
ENST00000636448.1:c.1316-52A>C
ENST00000636570.1:c.5098A>C	ENSP00000490183.1:p.Arg1700=
ENST00000636629.1:n.499A>C
ENST00000636633.1:n.2194-52A>C
ENST00000636999.1:n.570A>C
ENST00000637424.1:c.5170A>C	ENSP00000489769.1:p.Arg1724=
ENST00000288139.8:c.5203A>C	ENSP00000288139.3:p.Arg1735=
ENST00000350061.9:c.5143A>C	ENSP00000288133.5:p.Arg1715=
ENST00000422281.6:c.5098A>C	ENSP00000409174.2:p.Arg1700=
ENST00000481478.1:c.4222A>C	ENSP00000418014.1:p.Arg1408=
NM_000720.3:c.5203A>C	NP_000711.1:p.Arg1735=
NM_001128839.2:c.5098A>C	NP_001122311.1:p.Arg1700=
NM_001128840.2:c.5143A>C	NP_001122312.1:p.Arg1715=
XM_005265448.2:c.5098A>C	XP_005265505.1:p.Arg1700=
XM_011534094.1:c.5398A>C	XP_011532396.1:p.Arg1800=
XM_011534095.1:c.5287A>C	XP_011532397.1:p.Arg1763=
XM_011534096.1:c.5209A>C	XP_011532398.1:p.Arg1737=
XM_011534097.1:c.4861A>C	XP_011532399.1:p.Arg1621=
XM_011534098.1:c.4861A>C	XP_011532400.1:p.Arg1621=
XM_011534099.1:c.4486A>C	XP_011532401.1:p.Arg1496=
XM_011534100.1:c.5293A>C	XP_011532402.1:p.Arg1765=
XM_005265448.3:c.5098A>C	XP_005265505.1:p.Arg1700=
XM_011534094.2:c.5398A>C	XP_011532396.1:p.Arg1800=
XM_011534096.2:c.5209A>C	XP_011532398.1:p.Arg1737=
XM_011534097.2:c.4861A>C	XP_011532399.1:p.Arg1621=
XM_011534099.2:c.4486A>C	XP_011532401.1:p.Arg1496=
XM_011534100.2:c.5293A>C	XP_011532402.1:p.Arg1765=
XM_017007137.1:c.5398A>C	XP_016862626.1:p.Arg1800=
XM_017007138.1:c.5395A>C	XP_016862627.1:p.Arg1799=
XM_017007139.1:c.5398A>C	XP_016862628.1:p.Arg1800=
XM_017007140.1:c.5338A>C	XP_016862629.1:p.Arg1780=
XM_017007141.1:c.5338A>C	XP_016862630.1:p.Arg1780=
XM_017007142.1:c.5314A>C	XP_016862631.1:p.Arg1772=
XM_017007143.1:c.5314A>C	XP_016862632.1:p.Arg1772=
XM_017007144.1:c.5314A>C	XP_016862633.1:p.Arg1772=
XM_017007145.1:c.5269A>C	XP_016862634.1:p.Arg1757=
NM_001128840.3:c.5143A>C MANE Select	NP_001122312.1:p.Arg1715=
NM_000720.4:c.5203A>C MANE Plus Clinical	NP_000711.1:p.Arg1735=
NM_001128839.3:c.5098A>C	NP_001122311.1:p.Arg1700=