Canonical Allele Identifier: CA353251800

Gene: CACNA1D

Linked Data

• MyVariant Identifiers: chr3:g.53835432G>T (hg19) ; chr3:g.53801405G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5448G>T	ENSP00000418014.2:p.Gln1816His
ENST00000636633.2:n.2387G>T
ENST00000636999.2:n.823G>T
ENST00000288139.11:c.5448G>T MANE Plus Clinical	ENSP00000288139.3:p.Gln1816His
ENST00000350061.11:c.5388G>T MANE Select	ENSP00000288133.5:p.Gln1796His
ENST00000422281.7:c.5343G>T	ENSP00000409174.2:p.Gln1781His
ENST00000636448.1:c.1509G>T
ENST00000636570.1:c.5343G>T	ENSP00000490183.1:p.Gln1781His
ENST00000636629.1:n.744G>T
ENST00000636633.1:n.2387G>T
ENST00000636999.1:n.815G>T
ENST00000637424.1:c.5415G>T	ENSP00000489769.1:p.Gln1805His
ENST00000637844.1:n.142G>T
ENST00000288139.8:c.5448G>T	ENSP00000288139.3:p.Gln1816His
ENST00000350061.9:c.5388G>T	ENSP00000288133.5:p.Gln1796His
ENST00000422281.6:c.5343G>T	ENSP00000409174.2:p.Gln1781His
ENST00000481478.1:c.4467G>T	ENSP00000418014.1:p.Gln1489His
NM_000720.3:c.5448G>T	NP_000711.1:p.Gln1816His
NM_001128839.2:c.5343G>T	NP_001122311.1:p.Gln1781His
NM_001128840.2:c.5388G>T	NP_001122312.1:p.Gln1796His
XM_005265448.2:c.5343G>T	XP_005265505.1:p.Gln1781His
XM_011534094.1:c.5643G>T	XP_011532396.1:p.Gln1881His
XM_011534095.1:c.5532G>T	XP_011532397.1:p.Gln1844His
XM_011534096.1:c.5454G>T	XP_011532398.1:p.Gln1818His
XM_011534097.1:c.5106G>T	XP_011532399.1:p.Gln1702His
XM_011534098.1:c.5106G>T	XP_011532400.1:p.Gln1702His
XM_011534099.1:c.4731G>T	XP_011532401.1:p.Gln1577His
XM_011534100.1:c.5538G>T	XP_011532402.1:p.Gln1846His
XM_005265448.3:c.5343G>T	XP_005265505.1:p.Gln1781His
XM_011534094.2:c.5643G>T	XP_011532396.1:p.Gln1881His
XM_011534096.2:c.5454G>T	XP_011532398.1:p.Gln1818His
XM_011534097.2:c.5106G>T	XP_011532399.1:p.Gln1702His
XM_011534099.2:c.4731G>T	XP_011532401.1:p.Gln1577His
XM_011534100.2:c.5538G>T	XP_011532402.1:p.Gln1846His
XM_017007137.1:c.5643G>T	XP_016862626.1:p.Gln1881His
XM_017007138.1:c.5640G>T	XP_016862627.1:p.Gln1880His
XM_017007139.1:c.5643G>T	XP_016862628.1:p.Gln1881His
XM_017007140.1:c.5583G>T	XP_016862629.1:p.Gln1861His
XM_017007141.1:c.5583G>T	XP_016862630.1:p.Gln1861His
XM_017007142.1:c.5559G>T	XP_016862631.1:p.Gln1853His
XM_017007143.1:c.5559G>T	XP_016862632.1:p.Gln1853His
XM_017007144.1:c.5559G>T	XP_016862633.1:p.Gln1853His
XM_017007145.1:c.5514G>T	XP_016862634.1:p.Gln1838His
NM_001128840.3:c.5388G>T MANE Select	NP_001122312.1:p.Gln1796His
NM_000720.4:c.5448G>T MANE Plus Clinical	NP_000711.1:p.Gln1816His
NM_001128839.3:c.5343G>T	NP_001122311.1:p.Gln1781His