Canonical Allele Identifier: CA1365484178

Gene: CACNA1D

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801253A= , CM000665.2:g.53801253A=	GRCh38
NC_000003.11:g.53835280A= , CM000665.1:g.53835280A=	GRCh37
NC_000003.10:g.53810320A=	NCBI36
NG_032999.1:g.311205A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5296A=	ENSP00000418014.2:p.Ile1766=
ENST00000636633.2:n.2235A=
ENST00000636999.2:n.671A=
ENST00000288139.11:c.5296A= MANE Plus Clinical	ENSP00000288139.3:p.Ile1766=
ENST00000350061.11:c.5236A= MANE Select	ENSP00000288133.5:p.Ile1746=
ENST00000422281.7:c.5191A=	ENSP00000409174.2:p.Ile1731=
ENST00000636448.1:c.1357A=
ENST00000636570.1:c.5191A=	ENSP00000490183.1:p.Ile1731=
ENST00000636629.1:n.592A=
ENST00000636633.1:n.2235A=
ENST00000636999.1:n.663A=
ENST00000637424.1:c.5263A=	ENSP00000489769.1:p.Ile1755=
ENST00000288139.8:c.5296A=	ENSP00000288139.3:p.Ile1766=
ENST00000350061.9:c.5236A=	ENSP00000288133.5:p.Ile1746=
ENST00000422281.6:c.5191A=	ENSP00000409174.2:p.Ile1731=
ENST00000481478.1:c.4315A=	ENSP00000418014.1:p.Ile1439=
NM_000720.3:c.5296A=	NP_000711.1:p.Ile1766=
NM_001128839.2:c.5191A=	NP_001122311.1:p.Ile1731=
NM_001128840.2:c.5236A=	NP_001122312.1:p.Ile1746=
XM_005265448.2:c.5191A=	XP_005265505.1:p.Ile1731=
XM_011534094.1:c.5491A=	XP_011532396.1:p.Ile1831=
XM_011534095.1:c.5380A=	XP_011532397.1:p.Ile1794=
XM_011534096.1:c.5302A=	XP_011532398.1:p.Ile1768=
XM_011534097.1:c.4954A=	XP_011532399.1:p.Ile1652=
XM_011534098.1:c.4954A=	XP_011532400.1:p.Ile1652=
XM_011534099.1:c.4579A=	XP_011532401.1:p.Ile1527=
XM_011534100.1:c.5386A=	XP_011532402.1:p.Ile1796=
XM_005265448.3:c.5191A=	XP_005265505.1:p.Ile1731=
XM_011534094.2:c.5491A=	XP_011532396.1:p.Ile1831=
XM_011534096.2:c.5302A=	XP_011532398.1:p.Ile1768=
XM_011534097.2:c.4954A=	XP_011532399.1:p.Ile1652=
XM_011534099.2:c.4579A=	XP_011532401.1:p.Ile1527=
XM_011534100.2:c.5386A=	XP_011532402.1:p.Ile1796=
XM_017007137.1:c.5491A=	XP_016862626.1:p.Ile1831=
XM_017007138.1:c.5488A=	XP_016862627.1:p.Ile1830=
XM_017007139.1:c.5491A=	XP_016862628.1:p.Ile1831=
XM_017007140.1:c.5431A=	XP_016862629.1:p.Ile1811=
XM_017007141.1:c.5431A=	XP_016862630.1:p.Ile1811=
XM_017007142.1:c.5407A=	XP_016862631.1:p.Ile1803=
XM_017007143.1:c.5407A=	XP_016862632.1:p.Ile1803=
XM_017007144.1:c.5407A=	XP_016862633.1:p.Ile1803=
XM_017007145.1:c.5362A=	XP_016862634.1:p.Ile1788=
NM_001128840.3:c.5236A= MANE Select	NP_001122312.1:p.Ile1746=
NM_000720.4:c.5296A= MANE Plus Clinical	NP_000711.1:p.Ile1766=
NM_001128839.3:c.5191A=	NP_001122311.1:p.Ile1731=