Canonical Allele Identifier: CA353250582

Gene: CACNA1D

Linked Data

• MyVariant Identifiers: chr3:g.53835251T>C (hg19) ; chr3:g.53801224T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801224T>C , CM000665.2:g.53801224T>C	GRCh38
NC_000003.11:g.53835251T>C , CM000665.1:g.53835251T>C	GRCh37
NC_000003.10:g.53810291T>C	NCBI36
NG_032999.1:g.311176T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5267T>C	ENSP00000418014.2:p.Val1756Ala
ENST00000636633.2:n.2206T>C
ENST00000636999.2:n.642T>C
ENST00000288139.11:c.5267T>C MANE Plus Clinical	ENSP00000288139.3:p.Val1756Ala
ENST00000350061.11:c.5207T>C MANE Select	ENSP00000288133.5:p.Val1736Ala
ENST00000422281.7:c.5162T>C	ENSP00000409174.2:p.Val1721Ala
ENST00000636448.1:c.1328T>C
ENST00000636570.1:c.5162T>C	ENSP00000490183.1:p.Val1721Ala
ENST00000636629.1:n.563T>C
ENST00000636633.1:n.2206T>C
ENST00000636999.1:n.634T>C
ENST00000637424.1:c.5234T>C	ENSP00000489769.1:p.Val1745Ala
ENST00000288139.8:c.5267T>C	ENSP00000288139.3:p.Val1756Ala
ENST00000350061.9:c.5207T>C	ENSP00000288133.5:p.Val1736Ala
ENST00000422281.6:c.5162T>C	ENSP00000409174.2:p.Val1721Ala
ENST00000481478.1:c.4286T>C	ENSP00000418014.1:p.Val1429Ala
NM_000720.3:c.5267T>C	NP_000711.1:p.Val1756Ala
NM_001128839.2:c.5162T>C	NP_001122311.1:p.Val1721Ala
NM_001128840.2:c.5207T>C	NP_001122312.1:p.Val1736Ala
XM_005265448.2:c.5162T>C	XP_005265505.1:p.Val1721Ala
XM_011534094.1:c.5462T>C	XP_011532396.1:p.Val1821Ala
XM_011534095.1:c.5351T>C	XP_011532397.1:p.Val1784Ala
XM_011534096.1:c.5273T>C	XP_011532398.1:p.Val1758Ala
XM_011534097.1:c.4925T>C	XP_011532399.1:p.Val1642Ala
XM_011534098.1:c.4925T>C	XP_011532400.1:p.Val1642Ala
XM_011534099.1:c.4550T>C	XP_011532401.1:p.Val1517Ala
XM_011534100.1:c.5357T>C	XP_011532402.1:p.Val1786Ala
XM_005265448.3:c.5162T>C	XP_005265505.1:p.Val1721Ala
XM_011534094.2:c.5462T>C	XP_011532396.1:p.Val1821Ala
XM_011534096.2:c.5273T>C	XP_011532398.1:p.Val1758Ala
XM_011534097.2:c.4925T>C	XP_011532399.1:p.Val1642Ala
XM_011534099.2:c.4550T>C	XP_011532401.1:p.Val1517Ala
XM_011534100.2:c.5357T>C	XP_011532402.1:p.Val1786Ala
XM_017007137.1:c.5462T>C	XP_016862626.1:p.Val1821Ala
XM_017007138.1:c.5459T>C	XP_016862627.1:p.Val1820Ala
XM_017007139.1:c.5462T>C	XP_016862628.1:p.Val1821Ala
XM_017007140.1:c.5402T>C	XP_016862629.1:p.Val1801Ala
XM_017007141.1:c.5402T>C	XP_016862630.1:p.Val1801Ala
XM_017007142.1:c.5378T>C	XP_016862631.1:p.Val1793Ala
XM_017007143.1:c.5378T>C	XP_016862632.1:p.Val1793Ala
XM_017007144.1:c.5378T>C	XP_016862633.1:p.Val1793Ala
XM_017007145.1:c.5333T>C	XP_016862634.1:p.Val1778Ala
NM_001128840.3:c.5207T>C MANE Select	NP_001122312.1:p.Val1736Ala
NM_000720.4:c.5267T>C MANE Plus Clinical	NP_000711.1:p.Val1756Ala
NM_001128839.3:c.5162T>C	NP_001122311.1:p.Val1721Ala