Canonical Allele Identifier: CA353250092

Gene: CACNA1D

Linked Data

• MyVariant Identifiers: chr3:g.53835187A>T (hg19) ; chr3:g.53801160A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5203A>T	ENSP00000418014.2:p.Arg1735Trp
ENST00000636633.2:n.2194-52A>T
ENST00000636999.2:n.578A>T
ENST00000288139.11:c.5203A>T MANE Plus Clinical	ENSP00000288139.3:p.Arg1735Trp
ENST00000350061.11:c.5143A>T MANE Select	ENSP00000288133.5:p.Arg1715Trp
ENST00000422281.7:c.5098A>T	ENSP00000409174.2:p.Arg1700Trp
ENST00000636448.1:c.1316-52A>T
ENST00000636570.1:c.5098A>T	ENSP00000490183.1:p.Arg1700Trp
ENST00000636629.1:n.499A>T
ENST00000636633.1:n.2194-52A>T
ENST00000636999.1:n.570A>T
ENST00000637424.1:c.5170A>T	ENSP00000489769.1:p.Arg1724Trp
ENST00000288139.8:c.5203A>T	ENSP00000288139.3:p.Arg1735Trp
ENST00000350061.9:c.5143A>T	ENSP00000288133.5:p.Arg1715Trp
ENST00000422281.6:c.5098A>T	ENSP00000409174.2:p.Arg1700Trp
ENST00000481478.1:c.4222A>T	ENSP00000418014.1:p.Arg1408Trp
NM_000720.3:c.5203A>T	NP_000711.1:p.Arg1735Trp
NM_001128839.2:c.5098A>T	NP_001122311.1:p.Arg1700Trp
NM_001128840.2:c.5143A>T	NP_001122312.1:p.Arg1715Trp
XM_005265448.2:c.5098A>T	XP_005265505.1:p.Arg1700Trp
XM_011534094.1:c.5398A>T	XP_011532396.1:p.Arg1800Trp
XM_011534095.1:c.5287A>T	XP_011532397.1:p.Arg1763Trp
XM_011534096.1:c.5209A>T	XP_011532398.1:p.Arg1737Trp
XM_011534097.1:c.4861A>T	XP_011532399.1:p.Arg1621Trp
XM_011534098.1:c.4861A>T	XP_011532400.1:p.Arg1621Trp
XM_011534099.1:c.4486A>T	XP_011532401.1:p.Arg1496Trp
XM_011534100.1:c.5293A>T	XP_011532402.1:p.Arg1765Trp
XM_005265448.3:c.5098A>T	XP_005265505.1:p.Arg1700Trp
XM_011534094.2:c.5398A>T	XP_011532396.1:p.Arg1800Trp
XM_011534096.2:c.5209A>T	XP_011532398.1:p.Arg1737Trp
XM_011534097.2:c.4861A>T	XP_011532399.1:p.Arg1621Trp
XM_011534099.2:c.4486A>T	XP_011532401.1:p.Arg1496Trp
XM_011534100.2:c.5293A>T	XP_011532402.1:p.Arg1765Trp
XM_017007137.1:c.5398A>T	XP_016862626.1:p.Arg1800Trp
XM_017007138.1:c.5395A>T	XP_016862627.1:p.Arg1799Trp
XM_017007139.1:c.5398A>T	XP_016862628.1:p.Arg1800Trp
XM_017007140.1:c.5338A>T	XP_016862629.1:p.Arg1780Trp
XM_017007141.1:c.5338A>T	XP_016862630.1:p.Arg1780Trp
XM_017007142.1:c.5314A>T	XP_016862631.1:p.Arg1772Trp
XM_017007143.1:c.5314A>T	XP_016862632.1:p.Arg1772Trp
XM_017007144.1:c.5314A>T	XP_016862633.1:p.Arg1772Trp
XM_017007145.1:c.5269A>T	XP_016862634.1:p.Arg1757Trp
NM_001128840.3:c.5143A>T MANE Select	NP_001122312.1:p.Arg1715Trp
NM_000720.4:c.5203A>T MANE Plus Clinical	NP_000711.1:p.Arg1735Trp
NM_001128839.3:c.5098A>T	NP_001122311.1:p.Arg1700Trp