Canonical Allele Identifier: CA353251865

Gene: CACNA1D

Linked Data

• COSMIC: COSM4119342 ; COSM4119343
• MyVariant Identifiers: chr3:g.53835443G>C (hg19) ; chr3:g.53801416G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801416G>C , CM000665.2:g.53801416G>C	GRCh38
NC_000003.11:g.53835443G>C , CM000665.1:g.53835443G>C	GRCh37
NC_000003.10:g.53810483G>C	NCBI36
NG_032999.1:g.311368G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5459G>C	ENSP00000418014.2:p.Ser1820Thr
ENST00000636633.2:n.2398G>C
ENST00000636999.2:n.834G>C
ENST00000288139.11:c.5459G>C MANE Plus Clinical	ENSP00000288139.3:p.Ser1820Thr
ENST00000350061.11:c.5399G>C MANE Select	ENSP00000288133.5:p.Ser1800Thr
ENST00000422281.7:c.5354G>C	ENSP00000409174.2:p.Ser1785Thr
ENST00000636448.1:c.1520G>C
ENST00000636570.1:c.5354G>C	ENSP00000490183.1:p.Ser1785Thr
ENST00000636629.1:n.755G>C
ENST00000636633.1:n.2398G>C
ENST00000636999.1:n.826G>C
ENST00000637424.1:c.5426G>C	ENSP00000489769.1:p.Ser1809Thr
ENST00000637844.1:n.153G>C
ENST00000288139.8:c.5459G>C	ENSP00000288139.3:p.Ser1820Thr
ENST00000350061.9:c.5399G>C	ENSP00000288133.5:p.Ser1800Thr
ENST00000422281.6:c.5354G>C	ENSP00000409174.2:p.Ser1785Thr
ENST00000481478.1:c.4478G>C	ENSP00000418014.1:p.Ser1493Thr
NM_000720.3:c.5459G>C	NP_000711.1:p.Ser1820Thr
NM_001128839.2:c.5354G>C	NP_001122311.1:p.Ser1785Thr
NM_001128840.2:c.5399G>C	NP_001122312.1:p.Ser1800Thr
XM_005265448.2:c.5354G>C	XP_005265505.1:p.Ser1785Thr
XM_011534094.1:c.5654G>C	XP_011532396.1:p.Ser1885Thr
XM_011534095.1:c.5543G>C	XP_011532397.1:p.Ser1848Thr
XM_011534096.1:c.5465G>C	XP_011532398.1:p.Ser1822Thr
XM_011534097.1:c.5117G>C	XP_011532399.1:p.Ser1706Thr
XM_011534098.1:c.5117G>C	XP_011532400.1:p.Ser1706Thr
XM_011534099.1:c.4742G>C	XP_011532401.1:p.Ser1581Thr
XM_011534100.1:c.5549G>C	XP_011532402.1:p.Ser1850Thr
XM_005265448.3:c.5354G>C	XP_005265505.1:p.Ser1785Thr
XM_011534094.2:c.5654G>C	XP_011532396.1:p.Ser1885Thr
XM_011534096.2:c.5465G>C	XP_011532398.1:p.Ser1822Thr
XM_011534097.2:c.5117G>C	XP_011532399.1:p.Ser1706Thr
XM_011534099.2:c.4742G>C	XP_011532401.1:p.Ser1581Thr
XM_011534100.2:c.5549G>C	XP_011532402.1:p.Ser1850Thr
XM_017007137.1:c.5654G>C	XP_016862626.1:p.Ser1885Thr
XM_017007138.1:c.5651G>C	XP_016862627.1:p.Ser1884Thr
XM_017007139.1:c.5654G>C	XP_016862628.1:p.Ser1885Thr
XM_017007140.1:c.5594G>C	XP_016862629.1:p.Ser1865Thr
XM_017007141.1:c.5594G>C	XP_016862630.1:p.Ser1865Thr
XM_017007142.1:c.5570G>C	XP_016862631.1:p.Ser1857Thr
XM_017007143.1:c.5570G>C	XP_016862632.1:p.Ser1857Thr
XM_017007144.1:c.5570G>C	XP_016862633.1:p.Ser1857Thr
XM_017007145.1:c.5525G>C	XP_016862634.1:p.Ser1842Thr
NM_001128840.3:c.5399G>C MANE Select	NP_001122312.1:p.Ser1800Thr
NM_000720.4:c.5459G>C MANE Plus Clinical	NP_000711.1:p.Ser1820Thr
NM_001128839.3:c.5354G>C	NP_001122311.1:p.Ser1785Thr