Canonical Allele Identifier: CA353250512

Gene: CACNA1D

Linked Data

• gnomAD v4: 3-53801215-G-A
• COSMIC: COSM5865074 ; COSM5865075
• MyVariant Identifiers: chr3:g.53835242G>A (hg19) ; chr3:g.53801215G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801215G>A , CM000665.2:g.53801215G>A	GRCh38
NC_000003.11:g.53835242G>A , CM000665.1:g.53835242G>A	GRCh37
NC_000003.10:g.53810282G>A	NCBI36
NG_032999.1:g.311167G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5258G>A	ENSP00000418014.2:p.Gly1753Glu
ENST00000636633.2:n.2197G>A
ENST00000636999.2:n.633G>A
ENST00000288139.11:c.5258G>A MANE Plus Clinical	ENSP00000288139.3:p.Gly1753Glu
ENST00000350061.11:c.5198G>A MANE Select	ENSP00000288133.5:p.Gly1733Glu
ENST00000422281.7:c.5153G>A	ENSP00000409174.2:p.Gly1718Glu
ENST00000636448.1:c.1319G>A
ENST00000636570.1:c.5153G>A	ENSP00000490183.1:p.Gly1718Glu
ENST00000636629.1:n.554G>A
ENST00000636633.1:n.2197G>A
ENST00000636999.1:n.625G>A
ENST00000637424.1:c.5225G>A	ENSP00000489769.1:p.Gly1742Glu
ENST00000288139.8:c.5258G>A	ENSP00000288139.3:p.Gly1753Glu
ENST00000350061.9:c.5198G>A	ENSP00000288133.5:p.Gly1733Glu
ENST00000422281.6:c.5153G>A	ENSP00000409174.2:p.Gly1718Glu
ENST00000481478.1:c.4277G>A	ENSP00000418014.1:p.Gly1426Glu
NM_000720.3:c.5258G>A	NP_000711.1:p.Gly1753Glu
NM_001128839.2:c.5153G>A	NP_001122311.1:p.Gly1718Glu
NM_001128840.2:c.5198G>A	NP_001122312.1:p.Gly1733Glu
XM_005265448.2:c.5153G>A	XP_005265505.1:p.Gly1718Glu
XM_011534094.1:c.5453G>A	XP_011532396.1:p.Gly1818Glu
XM_011534095.1:c.5342G>A	XP_011532397.1:p.Gly1781Glu
XM_011534096.1:c.5264G>A	XP_011532398.1:p.Gly1755Glu
XM_011534097.1:c.4916G>A	XP_011532399.1:p.Gly1639Glu
XM_011534098.1:c.4916G>A	XP_011532400.1:p.Gly1639Glu
XM_011534099.1:c.4541G>A	XP_011532401.1:p.Gly1514Glu
XM_011534100.1:c.5348G>A	XP_011532402.1:p.Gly1783Glu
XM_005265448.3:c.5153G>A	XP_005265505.1:p.Gly1718Glu
XM_011534094.2:c.5453G>A	XP_011532396.1:p.Gly1818Glu
XM_011534096.2:c.5264G>A	XP_011532398.1:p.Gly1755Glu
XM_011534097.2:c.4916G>A	XP_011532399.1:p.Gly1639Glu
XM_011534099.2:c.4541G>A	XP_011532401.1:p.Gly1514Glu
XM_011534100.2:c.5348G>A	XP_011532402.1:p.Gly1783Glu
XM_017007137.1:c.5453G>A	XP_016862626.1:p.Gly1818Glu
XM_017007138.1:c.5450G>A	XP_016862627.1:p.Gly1817Glu
XM_017007139.1:c.5453G>A	XP_016862628.1:p.Gly1818Glu
XM_017007140.1:c.5393G>A	XP_016862629.1:p.Gly1798Glu
XM_017007141.1:c.5393G>A	XP_016862630.1:p.Gly1798Glu
XM_017007142.1:c.5369G>A	XP_016862631.1:p.Gly1790Glu
XM_017007143.1:c.5369G>A	XP_016862632.1:p.Gly1790Glu
XM_017007144.1:c.5369G>A	XP_016862633.1:p.Gly1790Glu
XM_017007145.1:c.5324G>A	XP_016862634.1:p.Gly1775Glu
NM_001128840.3:c.5198G>A MANE Select	NP_001122312.1:p.Gly1733Glu
NM_000720.4:c.5258G>A MANE Plus Clinical	NP_000711.1:p.Gly1753Glu
NM_001128839.3:c.5153G>A	NP_001122311.1:p.Gly1718Glu