Canonical Allele Identifier: CA433896010

Gene: CACNA1D

Linked Data

• MyVariant Identifiers: chr3:g.53835225G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801198G>C , CM000665.2:g.53801198G>C	GRCh38
NC_000003.11:g.53835225G>C , CM000665.1:g.53835225G>C	GRCh37
NC_000003.10:g.53810265G>C	NCBI36
NG_032999.1:g.311150G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5241G>C	ENSP00000418014.2:p.Pro1747=
ENST00000636633.2:n.2194-14G>C
ENST00000636999.2:n.616G>C
ENST00000288139.11:c.5241G>C MANE Plus Clinical	ENSP00000288139.3:p.Pro1747=
ENST00000350061.11:c.5181G>C MANE Select	ENSP00000288133.5:p.Pro1727=
ENST00000422281.7:c.5136G>C	ENSP00000409174.2:p.Pro1712=
ENST00000636448.1:c.1316-14G>C
ENST00000636570.1:c.5136G>C	ENSP00000490183.1:p.Pro1712=
ENST00000636629.1:n.537G>C
ENST00000636633.1:n.2194-14G>C
ENST00000636999.1:n.608G>C
ENST00000637424.1:c.5208G>C	ENSP00000489769.1:p.Pro1736=
ENST00000288139.8:c.5241G>C	ENSP00000288139.3:p.Pro1747=
ENST00000350061.9:c.5181G>C	ENSP00000288133.5:p.Pro1727=
ENST00000422281.6:c.5136G>C	ENSP00000409174.2:p.Pro1712=
ENST00000481478.1:c.4260G>C	ENSP00000418014.1:p.Pro1420=
NM_000720.3:c.5241G>C	NP_000711.1:p.Pro1747=
NM_001128839.2:c.5136G>C	NP_001122311.1:p.Pro1712=
NM_001128840.2:c.5181G>C	NP_001122312.1:p.Pro1727=
XM_005265448.2:c.5136G>C	XP_005265505.1:p.Pro1712=
XM_011534094.1:c.5436G>C	XP_011532396.1:p.Pro1812=
XM_011534095.1:c.5325G>C	XP_011532397.1:p.Pro1775=
XM_011534096.1:c.5247G>C	XP_011532398.1:p.Pro1749=
XM_011534097.1:c.4899G>C	XP_011532399.1:p.Pro1633=
XM_011534098.1:c.4899G>C	XP_011532400.1:p.Pro1633=
XM_011534099.1:c.4524G>C	XP_011532401.1:p.Pro1508=
XM_011534100.1:c.5331G>C	XP_011532402.1:p.Pro1777=
XM_005265448.3:c.5136G>C	XP_005265505.1:p.Pro1712=
XM_011534094.2:c.5436G>C	XP_011532396.1:p.Pro1812=
XM_011534096.2:c.5247G>C	XP_011532398.1:p.Pro1749=
XM_011534097.2:c.4899G>C	XP_011532399.1:p.Pro1633=
XM_011534099.2:c.4524G>C	XP_011532401.1:p.Pro1508=
XM_011534100.2:c.5331G>C	XP_011532402.1:p.Pro1777=
XM_017007137.1:c.5436G>C	XP_016862626.1:p.Pro1812=
XM_017007138.1:c.5433G>C	XP_016862627.1:p.Pro1811=
XM_017007139.1:c.5436G>C	XP_016862628.1:p.Pro1812=
XM_017007140.1:c.5376G>C	XP_016862629.1:p.Pro1792=
XM_017007141.1:c.5376G>C	XP_016862630.1:p.Pro1792=
XM_017007142.1:c.5352G>C	XP_016862631.1:p.Pro1784=
XM_017007143.1:c.5352G>C	XP_016862632.1:p.Pro1784=
XM_017007144.1:c.5352G>C	XP_016862633.1:p.Pro1784=
XM_017007145.1:c.5307G>C	XP_016862634.1:p.Pro1769=
NM_001128840.3:c.5181G>C MANE Select	NP_001122312.1:p.Pro1727=
NM_000720.4:c.5241G>C MANE Plus Clinical	NP_000711.1:p.Pro1747=
NM_001128839.3:c.5136G>C	NP_001122311.1:p.Pro1712=