Canonical Allele Identifier: CA353251743

Gene: CACNA1D

Linked Data

• MyVariant Identifiers: chr3:g.53835419A>T (hg19) ; chr3:g.53801392A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801392A>T , CM000665.2:g.53801392A>T	GRCh38
NC_000003.11:g.53835419A>T , CM000665.1:g.53835419A>T	GRCh37
NC_000003.10:g.53810459A>T	NCBI36
NG_032999.1:g.311344A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5435A>T	ENSP00000418014.2:p.Asp1812Val
ENST00000636633.2:n.2374A>T
ENST00000636999.2:n.810A>T
ENST00000288139.11:c.5435A>T MANE Plus Clinical	ENSP00000288139.3:p.Asp1812Val
ENST00000350061.11:c.5375A>T MANE Select	ENSP00000288133.5:p.Asp1792Val
ENST00000422281.7:c.5330A>T	ENSP00000409174.2:p.Asp1777Val
ENST00000636448.1:c.1496A>T
ENST00000636570.1:c.5330A>T	ENSP00000490183.1:p.Asp1777Val
ENST00000636629.1:n.731A>T
ENST00000636633.1:n.2374A>T
ENST00000636999.1:n.802A>T
ENST00000637424.1:c.5402A>T	ENSP00000489769.1:p.Asp1801Val
ENST00000637844.1:n.129A>T
ENST00000288139.8:c.5435A>T	ENSP00000288139.3:p.Asp1812Val
ENST00000350061.9:c.5375A>T	ENSP00000288133.5:p.Asp1792Val
ENST00000422281.6:c.5330A>T	ENSP00000409174.2:p.Asp1777Val
ENST00000481478.1:c.4454A>T	ENSP00000418014.1:p.Asp1485Val
NM_000720.3:c.5435A>T	NP_000711.1:p.Asp1812Val
NM_001128839.2:c.5330A>T	NP_001122311.1:p.Asp1777Val
NM_001128840.2:c.5375A>T	NP_001122312.1:p.Asp1792Val
XM_005265448.2:c.5330A>T	XP_005265505.1:p.Asp1777Val
XM_011534094.1:c.5630A>T	XP_011532396.1:p.Asp1877Val
XM_011534095.1:c.5519A>T	XP_011532397.1:p.Asp1840Val
XM_011534096.1:c.5441A>T	XP_011532398.1:p.Asp1814Val
XM_011534097.1:c.5093A>T	XP_011532399.1:p.Asp1698Val
XM_011534098.1:c.5093A>T	XP_011532400.1:p.Asp1698Val
XM_011534099.1:c.4718A>T	XP_011532401.1:p.Asp1573Val
XM_011534100.1:c.5525A>T	XP_011532402.1:p.Asp1842Val
XM_005265448.3:c.5330A>T	XP_005265505.1:p.Asp1777Val
XM_011534094.2:c.5630A>T	XP_011532396.1:p.Asp1877Val
XM_011534096.2:c.5441A>T	XP_011532398.1:p.Asp1814Val
XM_011534097.2:c.5093A>T	XP_011532399.1:p.Asp1698Val
XM_011534099.2:c.4718A>T	XP_011532401.1:p.Asp1573Val
XM_011534100.2:c.5525A>T	XP_011532402.1:p.Asp1842Val
XM_017007137.1:c.5630A>T	XP_016862626.1:p.Asp1877Val
XM_017007138.1:c.5627A>T	XP_016862627.1:p.Asp1876Val
XM_017007139.1:c.5630A>T	XP_016862628.1:p.Asp1877Val
XM_017007140.1:c.5570A>T	XP_016862629.1:p.Asp1857Val
XM_017007141.1:c.5570A>T	XP_016862630.1:p.Asp1857Val
XM_017007142.1:c.5546A>T	XP_016862631.1:p.Asp1849Val
XM_017007143.1:c.5546A>T	XP_016862632.1:p.Asp1849Val
XM_017007144.1:c.5546A>T	XP_016862633.1:p.Asp1849Val
XM_017007145.1:c.5501A>T	XP_016862634.1:p.Asp1834Val
NM_001128840.3:c.5375A>T MANE Select	NP_001122312.1:p.Asp1792Val
NM_000720.4:c.5435A>T MANE Plus Clinical	NP_000711.1:p.Asp1812Val
NM_001128839.3:c.5330A>T	NP_001122311.1:p.Asp1777Val