Canonical Allele Identifier: CA433804144

Gene: CACNA1D

Linked Data

• MyVariant Identifiers: chr3:g.53835429T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801402T>C , CM000665.2:g.53801402T>C	GRCh38
NC_000003.11:g.53835429T>C , CM000665.1:g.53835429T>C	GRCh37
NC_000003.10:g.53810469T>C	NCBI36
NG_032999.1:g.311354T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5445T>C	ENSP00000418014.2:p.Pro1815=
ENST00000636633.2:n.2384T>C
ENST00000636999.2:n.820T>C
ENST00000288139.11:c.5445T>C MANE Plus Clinical	ENSP00000288139.3:p.Pro1815=
ENST00000350061.11:c.5385T>C MANE Select	ENSP00000288133.5:p.Pro1795=
ENST00000422281.7:c.5340T>C	ENSP00000409174.2:p.Pro1780=
ENST00000636448.1:c.1506T>C
ENST00000636570.1:c.5340T>C	ENSP00000490183.1:p.Pro1780=
ENST00000636629.1:n.741T>C
ENST00000636633.1:n.2384T>C
ENST00000636999.1:n.812T>C
ENST00000637424.1:c.5412T>C	ENSP00000489769.1:p.Pro1804=
ENST00000637844.1:n.139T>C
ENST00000288139.8:c.5445T>C	ENSP00000288139.3:p.Pro1815=
ENST00000350061.9:c.5385T>C	ENSP00000288133.5:p.Pro1795=
ENST00000422281.6:c.5340T>C	ENSP00000409174.2:p.Pro1780=
ENST00000481478.1:c.4464T>C	ENSP00000418014.1:p.Pro1488=
NM_000720.3:c.5445T>C	NP_000711.1:p.Pro1815=
NM_001128839.2:c.5340T>C	NP_001122311.1:p.Pro1780=
NM_001128840.2:c.5385T>C	NP_001122312.1:p.Pro1795=
XM_005265448.2:c.5340T>C	XP_005265505.1:p.Pro1780=
XM_011534094.1:c.5640T>C	XP_011532396.1:p.Pro1880=
XM_011534095.1:c.5529T>C	XP_011532397.1:p.Pro1843=
XM_011534096.1:c.5451T>C	XP_011532398.1:p.Pro1817=
XM_011534097.1:c.5103T>C	XP_011532399.1:p.Pro1701=
XM_011534098.1:c.5103T>C	XP_011532400.1:p.Pro1701=
XM_011534099.1:c.4728T>C	XP_011532401.1:p.Pro1576=
XM_011534100.1:c.5535T>C	XP_011532402.1:p.Pro1845=
XM_005265448.3:c.5340T>C	XP_005265505.1:p.Pro1780=
XM_011534094.2:c.5640T>C	XP_011532396.1:p.Pro1880=
XM_011534096.2:c.5451T>C	XP_011532398.1:p.Pro1817=
XM_011534097.2:c.5103T>C	XP_011532399.1:p.Pro1701=
XM_011534099.2:c.4728T>C	XP_011532401.1:p.Pro1576=
XM_011534100.2:c.5535T>C	XP_011532402.1:p.Pro1845=
XM_017007137.1:c.5640T>C	XP_016862626.1:p.Pro1880=
XM_017007138.1:c.5637T>C	XP_016862627.1:p.Pro1879=
XM_017007139.1:c.5640T>C	XP_016862628.1:p.Pro1880=
XM_017007140.1:c.5580T>C	XP_016862629.1:p.Pro1860=
XM_017007141.1:c.5580T>C	XP_016862630.1:p.Pro1860=
XM_017007142.1:c.5556T>C	XP_016862631.1:p.Pro1852=
XM_017007143.1:c.5556T>C	XP_016862632.1:p.Pro1852=
XM_017007144.1:c.5556T>C	XP_016862633.1:p.Pro1852=
XM_017007145.1:c.5511T>C	XP_016862634.1:p.Pro1837=
NM_001128840.3:c.5385T>C MANE Select	NP_001122312.1:p.Pro1795=
NM_000720.4:c.5445T>C MANE Plus Clinical	NP_000711.1:p.Pro1815=
NM_001128839.3:c.5340T>C	NP_001122311.1:p.Pro1780=