Canonical Allele Identifier: CA1365484167

Gene: CACNA1D

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801220T= , CM000665.2:g.53801220T=	GRCh38
NC_000003.11:g.53835247T= , CM000665.1:g.53835247T=	GRCh37
NC_000003.10:g.53810287T=	NCBI36
NG_032999.1:g.311172T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5263T=	ENSP00000418014.2:p.Ser1755=
ENST00000636633.2:n.2202T=
ENST00000636999.2:n.638T=
ENST00000288139.11:c.5263T= MANE Plus Clinical	ENSP00000288139.3:p.Ser1755=
ENST00000350061.11:c.5203T= MANE Select	ENSP00000288133.5:p.Ser1735=
ENST00000422281.7:c.5158T=	ENSP00000409174.2:p.Ser1720=
ENST00000636448.1:c.1324T=
ENST00000636570.1:c.5158T=	ENSP00000490183.1:p.Ser1720=
ENST00000636629.1:n.559T=
ENST00000636633.1:n.2202T=
ENST00000636999.1:n.630T=
ENST00000637424.1:c.5230T=	ENSP00000489769.1:p.Ser1744=
ENST00000288139.8:c.5263T=	ENSP00000288139.3:p.Ser1755=
ENST00000350061.9:c.5203T=	ENSP00000288133.5:p.Ser1735=
ENST00000422281.6:c.5158T=	ENSP00000409174.2:p.Ser1720=
ENST00000481478.1:c.4282T=	ENSP00000418014.1:p.Ser1428=
NM_000720.3:c.5263T=	NP_000711.1:p.Ser1755=
NM_001128839.2:c.5158T=	NP_001122311.1:p.Ser1720=
NM_001128840.2:c.5203T=	NP_001122312.1:p.Ser1735=
XM_005265448.2:c.5158T=	XP_005265505.1:p.Ser1720=
XM_011534094.1:c.5458T=	XP_011532396.1:p.Ser1820=
XM_011534095.1:c.5347T=	XP_011532397.1:p.Ser1783=
XM_011534096.1:c.5269T=	XP_011532398.1:p.Ser1757=
XM_011534097.1:c.4921T=	XP_011532399.1:p.Ser1641=
XM_011534098.1:c.4921T=	XP_011532400.1:p.Ser1641=
XM_011534099.1:c.4546T=	XP_011532401.1:p.Ser1516=
XM_011534100.1:c.5353T=	XP_011532402.1:p.Ser1785=
XM_005265448.3:c.5158T=	XP_005265505.1:p.Ser1720=
XM_011534094.2:c.5458T=	XP_011532396.1:p.Ser1820=
XM_011534096.2:c.5269T=	XP_011532398.1:p.Ser1757=
XM_011534097.2:c.4921T=	XP_011532399.1:p.Ser1641=
XM_011534099.2:c.4546T=	XP_011532401.1:p.Ser1516=
XM_011534100.2:c.5353T=	XP_011532402.1:p.Ser1785=
XM_017007137.1:c.5458T=	XP_016862626.1:p.Ser1820=
XM_017007138.1:c.5455T=	XP_016862627.1:p.Ser1819=
XM_017007139.1:c.5458T=	XP_016862628.1:p.Ser1820=
XM_017007140.1:c.5398T=	XP_016862629.1:p.Ser1800=
XM_017007141.1:c.5398T=	XP_016862630.1:p.Ser1800=
XM_017007142.1:c.5374T=	XP_016862631.1:p.Ser1792=
XM_017007143.1:c.5374T=	XP_016862632.1:p.Ser1792=
XM_017007144.1:c.5374T=	XP_016862633.1:p.Ser1792=
XM_017007145.1:c.5329T=	XP_016862634.1:p.Ser1777=
NM_001128840.3:c.5203T= MANE Select	NP_001122312.1:p.Ser1735=
NM_000720.4:c.5263T= MANE Plus Clinical	NP_000711.1:p.Ser1755=
NM_001128839.3:c.5158T=	NP_001122311.1:p.Ser1720=