Canonical Allele Identifier: CA353250012

Gene: CACNA1D

Linked Data

• MyVariant Identifiers: chr3:g.53835172C>A (hg19) ; chr3:g.53801145C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801145C>A , CM000665.2:g.53801145C>A	GRCh38
NC_000003.11:g.53835172C>A , CM000665.1:g.53835172C>A	GRCh37
NC_000003.10:g.53810212C>A	NCBI36
NG_032999.1:g.311097C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5188C>A	ENSP00000418014.2:p.Pro1730Thr
ENST00000636633.2:n.2194-67C>A
ENST00000636999.2:n.563C>A
ENST00000288139.11:c.5188C>A MANE Plus Clinical	ENSP00000288139.3:p.Pro1730Thr
ENST00000350061.11:c.5128C>A MANE Select	ENSP00000288133.5:p.Pro1710Thr
ENST00000422281.7:c.5083C>A	ENSP00000409174.2:p.Pro1695Thr
ENST00000636448.1:c.1316-67C>A
ENST00000636570.1:c.5083C>A	ENSP00000490183.1:p.Pro1695Thr
ENST00000636629.1:n.484C>A
ENST00000636633.1:n.2194-67C>A
ENST00000636999.1:n.555C>A
ENST00000637424.1:c.5155C>A	ENSP00000489769.1:p.Pro1719Thr
ENST00000288139.8:c.5188C>A	ENSP00000288139.3:p.Pro1730Thr
ENST00000350061.9:c.5128C>A	ENSP00000288133.5:p.Pro1710Thr
ENST00000422281.6:c.5083C>A	ENSP00000409174.2:p.Pro1695Thr
ENST00000481478.1:c.4207C>A	ENSP00000418014.1:p.Pro1403Thr
NM_000720.3:c.5188C>A	NP_000711.1:p.Pro1730Thr
NM_001128839.2:c.5083C>A	NP_001122311.1:p.Pro1695Thr
NM_001128840.2:c.5128C>A	NP_001122312.1:p.Pro1710Thr
XM_005265448.2:c.5083C>A	XP_005265505.1:p.Pro1695Thr
XM_011534094.1:c.5383C>A	XP_011532396.1:p.Pro1795Thr
XM_011534095.1:c.5272C>A	XP_011532397.1:p.Pro1758Thr
XM_011534096.1:c.5194C>A	XP_011532398.1:p.Pro1732Thr
XM_011534097.1:c.4846C>A	XP_011532399.1:p.Pro1616Thr
XM_011534098.1:c.4846C>A	XP_011532400.1:p.Pro1616Thr
XM_011534099.1:c.4471C>A	XP_011532401.1:p.Pro1491Thr
XM_011534100.1:c.5278C>A	XP_011532402.1:p.Pro1760Thr
XM_005265448.3:c.5083C>A	XP_005265505.1:p.Pro1695Thr
XM_011534094.2:c.5383C>A	XP_011532396.1:p.Pro1795Thr
XM_011534096.2:c.5194C>A	XP_011532398.1:p.Pro1732Thr
XM_011534097.2:c.4846C>A	XP_011532399.1:p.Pro1616Thr
XM_011534099.2:c.4471C>A	XP_011532401.1:p.Pro1491Thr
XM_011534100.2:c.5278C>A	XP_011532402.1:p.Pro1760Thr
XM_017007137.1:c.5383C>A	XP_016862626.1:p.Pro1795Thr
XM_017007138.1:c.5380C>A	XP_016862627.1:p.Pro1794Thr
XM_017007139.1:c.5383C>A	XP_016862628.1:p.Pro1795Thr
XM_017007140.1:c.5323C>A	XP_016862629.1:p.Pro1775Thr
XM_017007141.1:c.5323C>A	XP_016862630.1:p.Pro1775Thr
XM_017007142.1:c.5299C>A	XP_016862631.1:p.Pro1767Thr
XM_017007143.1:c.5299C>A	XP_016862632.1:p.Pro1767Thr
XM_017007144.1:c.5299C>A	XP_016862633.1:p.Pro1767Thr
XM_017007145.1:c.5254C>A	XP_016862634.1:p.Pro1752Thr
NM_001128840.3:c.5128C>A MANE Select	NP_001122312.1:p.Pro1710Thr
NM_000720.4:c.5188C>A MANE Plus Clinical	NP_000711.1:p.Pro1730Thr
NM_001128839.3:c.5083C>A	NP_001122311.1:p.Pro1695Thr