Canonical Allele Identifier: CA353250022

Gene: CACNA1D

Linked Data

• MyVariant Identifiers: chr3:g.53835173C>G (hg19) ; chr3:g.53801146C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801146C>G , CM000665.2:g.53801146C>G	GRCh38
NC_000003.11:g.53835173C>G , CM000665.1:g.53835173C>G	GRCh37
NC_000003.10:g.53810213C>G	NCBI36
NG_032999.1:g.311098C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5189C>G	ENSP00000418014.2:p.Pro1730Arg
ENST00000636633.2:n.2194-66C>G
ENST00000636999.2:n.564C>G
ENST00000288139.11:c.5189C>G MANE Plus Clinical	ENSP00000288139.3:p.Pro1730Arg
ENST00000350061.11:c.5129C>G MANE Select	ENSP00000288133.5:p.Pro1710Arg
ENST00000422281.7:c.5084C>G	ENSP00000409174.2:p.Pro1695Arg
ENST00000636448.1:c.1316-66C>G
ENST00000636570.1:c.5084C>G	ENSP00000490183.1:p.Pro1695Arg
ENST00000636629.1:n.485C>G
ENST00000636633.1:n.2194-66C>G
ENST00000636999.1:n.556C>G
ENST00000637424.1:c.5156C>G	ENSP00000489769.1:p.Pro1719Arg
ENST00000288139.8:c.5189C>G	ENSP00000288139.3:p.Pro1730Arg
ENST00000350061.9:c.5129C>G	ENSP00000288133.5:p.Pro1710Arg
ENST00000422281.6:c.5084C>G	ENSP00000409174.2:p.Pro1695Arg
ENST00000481478.1:c.4208C>G	ENSP00000418014.1:p.Pro1403Arg
NM_000720.3:c.5189C>G	NP_000711.1:p.Pro1730Arg
NM_001128839.2:c.5084C>G	NP_001122311.1:p.Pro1695Arg
NM_001128840.2:c.5129C>G	NP_001122312.1:p.Pro1710Arg
XM_005265448.2:c.5084C>G	XP_005265505.1:p.Pro1695Arg
XM_011534094.1:c.5384C>G	XP_011532396.1:p.Pro1795Arg
XM_011534095.1:c.5273C>G	XP_011532397.1:p.Pro1758Arg
XM_011534096.1:c.5195C>G	XP_011532398.1:p.Pro1732Arg
XM_011534097.1:c.4847C>G	XP_011532399.1:p.Pro1616Arg
XM_011534098.1:c.4847C>G	XP_011532400.1:p.Pro1616Arg
XM_011534099.1:c.4472C>G	XP_011532401.1:p.Pro1491Arg
XM_011534100.1:c.5279C>G	XP_011532402.1:p.Pro1760Arg
XM_005265448.3:c.5084C>G	XP_005265505.1:p.Pro1695Arg
XM_011534094.2:c.5384C>G	XP_011532396.1:p.Pro1795Arg
XM_011534096.2:c.5195C>G	XP_011532398.1:p.Pro1732Arg
XM_011534097.2:c.4847C>G	XP_011532399.1:p.Pro1616Arg
XM_011534099.2:c.4472C>G	XP_011532401.1:p.Pro1491Arg
XM_011534100.2:c.5279C>G	XP_011532402.1:p.Pro1760Arg
XM_017007137.1:c.5384C>G	XP_016862626.1:p.Pro1795Arg
XM_017007138.1:c.5381C>G	XP_016862627.1:p.Pro1794Arg
XM_017007139.1:c.5384C>G	XP_016862628.1:p.Pro1795Arg
XM_017007140.1:c.5324C>G	XP_016862629.1:p.Pro1775Arg
XM_017007141.1:c.5324C>G	XP_016862630.1:p.Pro1775Arg
XM_017007142.1:c.5300C>G	XP_016862631.1:p.Pro1767Arg
XM_017007143.1:c.5300C>G	XP_016862632.1:p.Pro1767Arg
XM_017007144.1:c.5300C>G	XP_016862633.1:p.Pro1767Arg
XM_017007145.1:c.5255C>G	XP_016862634.1:p.Pro1752Arg
NM_001128840.3:c.5129C>G MANE Select	NP_001122312.1:p.Pro1710Arg
NM_000720.4:c.5189C>G MANE Plus Clinical	NP_000711.1:p.Pro1730Arg
NM_001128839.3:c.5084C>G	NP_001122311.1:p.Pro1695Arg