Canonical Allele Identifier: CA353259382

Gene: CACNA1D

Linked Data

• MyVariant Identifiers: chr3:g.53845326G>C (hg19) ; chr3:g.53811299G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53811299G>C , CM000665.2:g.53811299G>C	GRCh38
NC_000003.11:g.53845326G>C , CM000665.1:g.53845326G>C	GRCh37
NC_000003.10:g.53820366G>C	NCBI36
NG_032999.1:g.321251G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.6439G>C	ENSP00000418014.2:p.Asp2147His
ENST00000636581.2:n.1768G>C
ENST00000636633.2:n.3378G>C
ENST00000636999.2:n.1814G>C
ENST00000288139.11:c.6439G>C MANE Plus Clinical	ENSP00000288139.3:p.Asp2147His
ENST00000350061.11:c.6379G>C MANE Select	ENSP00000288133.5:p.Asp2127His
ENST00000422281.7:c.6307G>C	ENSP00000409174.2:p.Asp2103His
ENST00000636448.1:c.2500G>C
ENST00000636570.1:c.6334G>C	ENSP00000490183.1:p.Asp2112His
ENST00000636581.1:n.1768G>C
ENST00000636633.1:n.3378G>C
ENST00000636999.1:n.1806G>C
ENST00000637424.1:c.6406G>C	ENSP00000489769.1:p.Asp2136His
ENST00000288139.8:c.6439G>C	ENSP00000288139.3:p.Asp2147His
ENST00000350061.9:c.6379G>C	ENSP00000288133.5:p.Asp2127His
ENST00000422281.6:c.6307G>C	ENSP00000409174.2:p.Asp2103His
ENST00000481478.1:c.5458G>C	ENSP00000418014.1:p.Asp1820His
NM_000720.3:c.6439G>C	NP_000711.1:p.Asp2147His
NM_001128839.2:c.6307G>C	NP_001122311.1:p.Asp2103His
NM_001128840.2:c.6379G>C	NP_001122312.1:p.Asp2127His
XM_005265448.2:c.6334G>C	XP_005265505.1:p.Asp2112His
XM_011534094.1:c.6634G>C	XP_011532396.1:p.Asp2212His
XM_011534095.1:c.6523G>C	XP_011532397.1:p.Asp2175His
XM_011534096.1:c.6445G>C	XP_011532398.1:p.Asp2149His
XM_011534097.1:c.6097G>C	XP_011532399.1:p.Asp2033His
XM_011534098.1:c.6097G>C	XP_011532400.1:p.Asp2033His
XM_011534099.1:c.5722G>C	XP_011532401.1:p.Asp1908His
XM_011534100.1:c.6529G>C	XP_011532402.1:p.Asp2177His
XM_005265448.3:c.6334G>C	XP_005265505.1:p.Asp2112His
XM_011534094.2:c.6634G>C	XP_011532396.1:p.Asp2212His
XM_011534096.2:c.6445G>C	XP_011532398.1:p.Asp2149His
XM_011534097.2:c.6097G>C	XP_011532399.1:p.Asp2033His
XM_011534099.2:c.5722G>C	XP_011532401.1:p.Asp1908His
XM_011534100.2:c.6529G>C	XP_011532402.1:p.Asp2177His
XM_017007137.1:c.6634G>C	XP_016862626.1:p.Asp2212His
XM_017007138.1:c.6631G>C	XP_016862627.1:p.Asp2211His
XM_017007139.1:c.6607G>C	XP_016862628.1:p.Asp2203His
XM_017007140.1:c.6574G>C	XP_016862629.1:p.Asp2192His
XM_017007141.1:c.6574G>C	XP_016862630.1:p.Asp2192His
XM_017007142.1:c.6550G>C	XP_016862631.1:p.Asp2184His
XM_017007143.1:c.6550G>C	XP_016862632.1:p.Asp2184His
XM_017007144.1:c.6550G>C	XP_016862633.1:p.Asp2184His
XM_017007145.1:c.6505G>C	XP_016862634.1:p.Asp2169His
NM_001128840.3:c.6379G>C MANE Select	NP_001122312.1:p.Asp2127His
NM_000720.4:c.6439G>C MANE Plus Clinical	NP_000711.1:p.Asp2147His
NM_001128839.3:c.6307G>C	NP_001122311.1:p.Asp2103His