Canonical Allele Identifier: CA353250039

Gene: CACNA1D

Linked Data

• gnomAD v4: 3-53801151-C-T
• MyVariant Identifiers: chr3:g.53835178C>T (hg19) ; chr3:g.53801151C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801151C>T , CM000665.2:g.53801151C>T	GRCh38
NC_000003.11:g.53835178C>T , CM000665.1:g.53835178C>T	GRCh37
NC_000003.10:g.53810218C>T	NCBI36
NG_032999.1:g.311103C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5194C>T	ENSP00000418014.2:p.His1732Tyr
ENST00000636633.2:n.2194-61C>T
ENST00000636999.2:n.569C>T
ENST00000288139.11:c.5194C>T MANE Plus Clinical	ENSP00000288139.3:p.His1732Tyr
ENST00000350061.11:c.5134C>T MANE Select	ENSP00000288133.5:p.His1712Tyr
ENST00000422281.7:c.5089C>T	ENSP00000409174.2:p.His1697Tyr
ENST00000636448.1:c.1316-61C>T
ENST00000636570.1:c.5089C>T	ENSP00000490183.1:p.His1697Tyr
ENST00000636629.1:n.490C>T
ENST00000636633.1:n.2194-61C>T
ENST00000636999.1:n.561C>T
ENST00000637424.1:c.5161C>T	ENSP00000489769.1:p.His1721Tyr
ENST00000288139.8:c.5194C>T	ENSP00000288139.3:p.His1732Tyr
ENST00000350061.9:c.5134C>T	ENSP00000288133.5:p.His1712Tyr
ENST00000422281.6:c.5089C>T	ENSP00000409174.2:p.His1697Tyr
ENST00000481478.1:c.4213C>T	ENSP00000418014.1:p.His1405Tyr
NM_000720.3:c.5194C>T	NP_000711.1:p.His1732Tyr
NM_001128839.2:c.5089C>T	NP_001122311.1:p.His1697Tyr
NM_001128840.2:c.5134C>T	NP_001122312.1:p.His1712Tyr
XM_005265448.2:c.5089C>T	XP_005265505.1:p.His1697Tyr
XM_011534094.1:c.5389C>T	XP_011532396.1:p.His1797Tyr
XM_011534095.1:c.5278C>T	XP_011532397.1:p.His1760Tyr
XM_011534096.1:c.5200C>T	XP_011532398.1:p.His1734Tyr
XM_011534097.1:c.4852C>T	XP_011532399.1:p.His1618Tyr
XM_011534098.1:c.4852C>T	XP_011532400.1:p.His1618Tyr
XM_011534099.1:c.4477C>T	XP_011532401.1:p.His1493Tyr
XM_011534100.1:c.5284C>T	XP_011532402.1:p.His1762Tyr
XM_005265448.3:c.5089C>T	XP_005265505.1:p.His1697Tyr
XM_011534094.2:c.5389C>T	XP_011532396.1:p.His1797Tyr
XM_011534096.2:c.5200C>T	XP_011532398.1:p.His1734Tyr
XM_011534097.2:c.4852C>T	XP_011532399.1:p.His1618Tyr
XM_011534099.2:c.4477C>T	XP_011532401.1:p.His1493Tyr
XM_011534100.2:c.5284C>T	XP_011532402.1:p.His1762Tyr
XM_017007137.1:c.5389C>T	XP_016862626.1:p.His1797Tyr
XM_017007138.1:c.5386C>T	XP_016862627.1:p.His1796Tyr
XM_017007139.1:c.5389C>T	XP_016862628.1:p.His1797Tyr
XM_017007140.1:c.5329C>T	XP_016862629.1:p.His1777Tyr
XM_017007141.1:c.5329C>T	XP_016862630.1:p.His1777Tyr
XM_017007142.1:c.5305C>T	XP_016862631.1:p.His1769Tyr
XM_017007143.1:c.5305C>T	XP_016862632.1:p.His1769Tyr
XM_017007144.1:c.5305C>T	XP_016862633.1:p.His1769Tyr
XM_017007145.1:c.5260C>T	XP_016862634.1:p.His1754Tyr
NM_001128840.3:c.5134C>T MANE Select	NP_001122312.1:p.His1712Tyr
NM_000720.4:c.5194C>T MANE Plus Clinical	NP_000711.1:p.His1732Tyr
NM_001128839.3:c.5089C>T	NP_001122311.1:p.His1697Tyr