Canonical Allele Identifier: CA433804147

Gene: CACNA1D

Linked Data

• MyVariant Identifiers: chr3:g.53835432G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801405G>A , CM000665.2:g.53801405G>A	GRCh38
NC_000003.11:g.53835432G>A , CM000665.1:g.53835432G>A	GRCh37
NC_000003.10:g.53810472G>A	NCBI36
NG_032999.1:g.311357G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5448G>A	ENSP00000418014.2:p.Gln1816=
ENST00000636633.2:n.2387G>A
ENST00000636999.2:n.823G>A
ENST00000288139.11:c.5448G>A MANE Plus Clinical	ENSP00000288139.3:p.Gln1816=
ENST00000350061.11:c.5388G>A MANE Select	ENSP00000288133.5:p.Gln1796=
ENST00000422281.7:c.5343G>A	ENSP00000409174.2:p.Gln1781=
ENST00000636448.1:c.1509G>A
ENST00000636570.1:c.5343G>A	ENSP00000490183.1:p.Gln1781=
ENST00000636629.1:n.744G>A
ENST00000636633.1:n.2387G>A
ENST00000636999.1:n.815G>A
ENST00000637424.1:c.5415G>A	ENSP00000489769.1:p.Gln1805=
ENST00000637844.1:n.142G>A
ENST00000288139.8:c.5448G>A	ENSP00000288139.3:p.Gln1816=
ENST00000350061.9:c.5388G>A	ENSP00000288133.5:p.Gln1796=
ENST00000422281.6:c.5343G>A	ENSP00000409174.2:p.Gln1781=
ENST00000481478.1:c.4467G>A	ENSP00000418014.1:p.Gln1489=
NM_000720.3:c.5448G>A	NP_000711.1:p.Gln1816=
NM_001128839.2:c.5343G>A	NP_001122311.1:p.Gln1781=
NM_001128840.2:c.5388G>A	NP_001122312.1:p.Gln1796=
XM_005265448.2:c.5343G>A	XP_005265505.1:p.Gln1781=
XM_011534094.1:c.5643G>A	XP_011532396.1:p.Gln1881=
XM_011534095.1:c.5532G>A	XP_011532397.1:p.Gln1844=
XM_011534096.1:c.5454G>A	XP_011532398.1:p.Gln1818=
XM_011534097.1:c.5106G>A	XP_011532399.1:p.Gln1702=
XM_011534098.1:c.5106G>A	XP_011532400.1:p.Gln1702=
XM_011534099.1:c.4731G>A	XP_011532401.1:p.Gln1577=
XM_011534100.1:c.5538G>A	XP_011532402.1:p.Gln1846=
XM_005265448.3:c.5343G>A	XP_005265505.1:p.Gln1781=
XM_011534094.2:c.5643G>A	XP_011532396.1:p.Gln1881=
XM_011534096.2:c.5454G>A	XP_011532398.1:p.Gln1818=
XM_011534097.2:c.5106G>A	XP_011532399.1:p.Gln1702=
XM_011534099.2:c.4731G>A	XP_011532401.1:p.Gln1577=
XM_011534100.2:c.5538G>A	XP_011532402.1:p.Gln1846=
XM_017007137.1:c.5643G>A	XP_016862626.1:p.Gln1881=
XM_017007138.1:c.5640G>A	XP_016862627.1:p.Gln1880=
XM_017007139.1:c.5643G>A	XP_016862628.1:p.Gln1881=
XM_017007140.1:c.5583G>A	XP_016862629.1:p.Gln1861=
XM_017007141.1:c.5583G>A	XP_016862630.1:p.Gln1861=
XM_017007142.1:c.5559G>A	XP_016862631.1:p.Gln1853=
XM_017007143.1:c.5559G>A	XP_016862632.1:p.Gln1853=
XM_017007144.1:c.5559G>A	XP_016862633.1:p.Gln1853=
XM_017007145.1:c.5514G>A	XP_016862634.1:p.Gln1838=
NM_001128840.3:c.5388G>A MANE Select	NP_001122312.1:p.Gln1796=
NM_000720.4:c.5448G>A MANE Plus Clinical	NP_000711.1:p.Gln1816=
NM_001128839.3:c.5343G>A	NP_001122311.1:p.Gln1781=