Canonical Allele Identifier: CA1365484181

Gene: CACNA1D

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801265G= , CM000665.2:g.53801265G=	GRCh38
NC_000003.11:g.53835292G= , CM000665.1:g.53835292G=	GRCh37
NC_000003.10:g.53810332G=	NCBI36
NG_032999.1:g.311217G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5308G=	ENSP00000418014.2:p.Val1770=
ENST00000636633.2:n.2247G=
ENST00000636999.2:n.683G=
ENST00000288139.11:c.5308G= MANE Plus Clinical	ENSP00000288139.3:p.Val1770=
ENST00000350061.11:c.5248G= MANE Select	ENSP00000288133.5:p.Val1750=
ENST00000422281.7:c.5203G=	ENSP00000409174.2:p.Val1735=
ENST00000636448.1:c.1369G=
ENST00000636570.1:c.5203G=	ENSP00000490183.1:p.Val1735=
ENST00000636629.1:n.604G=
ENST00000636633.1:n.2247G=
ENST00000636999.1:n.675G=
ENST00000637424.1:c.5275G=	ENSP00000489769.1:p.Val1759=
ENST00000637844.1:n.2G=
ENST00000288139.8:c.5308G=	ENSP00000288139.3:p.Val1770=
ENST00000350061.9:c.5248G=	ENSP00000288133.5:p.Val1750=
ENST00000422281.6:c.5203G=	ENSP00000409174.2:p.Val1735=
ENST00000481478.1:c.4327G=	ENSP00000418014.1:p.Val1443=
NM_000720.3:c.5308G=	NP_000711.1:p.Val1770=
NM_001128839.2:c.5203G=	NP_001122311.1:p.Val1735=
NM_001128840.2:c.5248G=	NP_001122312.1:p.Val1750=
XM_005265448.2:c.5203G=	XP_005265505.1:p.Val1735=
XM_011534094.1:c.5503G=	XP_011532396.1:p.Val1835=
XM_011534095.1:c.5392G=	XP_011532397.1:p.Val1798=
XM_011534096.1:c.5314G=	XP_011532398.1:p.Val1772=
XM_011534097.1:c.4966G=	XP_011532399.1:p.Val1656=
XM_011534098.1:c.4966G=	XP_011532400.1:p.Val1656=
XM_011534099.1:c.4591G=	XP_011532401.1:p.Val1531=
XM_011534100.1:c.5398G=	XP_011532402.1:p.Val1800=
XM_005265448.3:c.5203G=	XP_005265505.1:p.Val1735=
XM_011534094.2:c.5503G=	XP_011532396.1:p.Val1835=
XM_011534096.2:c.5314G=	XP_011532398.1:p.Val1772=
XM_011534097.2:c.4966G=	XP_011532399.1:p.Val1656=
XM_011534099.2:c.4591G=	XP_011532401.1:p.Val1531=
XM_011534100.2:c.5398G=	XP_011532402.1:p.Val1800=
XM_017007137.1:c.5503G=	XP_016862626.1:p.Val1835=
XM_017007138.1:c.5500G=	XP_016862627.1:p.Val1834=
XM_017007139.1:c.5503G=	XP_016862628.1:p.Val1835=
XM_017007140.1:c.5443G=	XP_016862629.1:p.Val1815=
XM_017007141.1:c.5443G=	XP_016862630.1:p.Val1815=
XM_017007142.1:c.5419G=	XP_016862631.1:p.Val1807=
XM_017007143.1:c.5419G=	XP_016862632.1:p.Val1807=
XM_017007144.1:c.5419G=	XP_016862633.1:p.Val1807=
XM_017007145.1:c.5374G=	XP_016862634.1:p.Val1792=
NM_001128840.3:c.5248G= MANE Select	NP_001122312.1:p.Val1750=
NM_000720.4:c.5308G= MANE Plus Clinical	NP_000711.1:p.Val1770=
NM_001128839.3:c.5203G=	NP_001122311.1:p.Val1735=