Canonical Allele Identifier: CA1365489048
Gene: CACNA1D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53811349C= , CM000665.2:g.53811349C= GRCh38
NC_000003.11:g.53845376C= , CM000665.1:g.53845376C= GRCh37
NC_000003.10:g.53820416C= NCBI36
NG_032999.1:g.321301C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000481478.2:c.6489C= ENSP00000418014.2:p.Asp2163=
ENST00000636581.2:n.1818C=
ENST00000636633.2:n.3428C=
ENST00000636999.2:n.1864C=
ENST00000288139.11:c.6489C= MANE Plus Clinical ENSP00000288139.3:p.Asp2163=
ENST00000350061.11:c.6429C= MANE Select ENSP00000288133.5:p.Asp2143=
ENST00000422281.7:c.6357C= ENSP00000409174.2:p.Asp2119=
ENST00000636448.1:c.2550C=
ENST00000636570.1:c.6384C= ENSP00000490183.1:p.Asp2128=
ENST00000636581.1:n.1818C=
ENST00000636633.1:n.3428C=
ENST00000636999.1:n.1856C=
ENST00000637424.1:c.6456C= ENSP00000489769.1:p.Asp2152=
ENST00000288139.8:c.6489C= ENSP00000288139.3:p.Asp2163=
ENST00000350061.9:c.6429C= ENSP00000288133.5:p.Asp2143=
ENST00000422281.6:c.6357C= ENSP00000409174.2:p.Asp2119=
ENST00000481478.1:c.5508C= ENSP00000418014.1:p.Asp1836=
NM_000720.3:c.6489C= NP_000711.1:p.Asp2163=
NM_001128839.2:c.6357C= NP_001122311.1:p.Asp2119=
NM_001128840.2:c.6429C= NP_001122312.1:p.Asp2143=
XM_005265448.2:c.6384C= XP_005265505.1:p.Asp2128=
XM_011534094.1:c.6684C= XP_011532396.1:p.Asp2228=
XM_011534095.1:c.6573C= XP_011532397.1:p.Asp2191=
XM_011534096.1:c.6495C= XP_011532398.1:p.Asp2165=
XM_011534097.1:c.6147C= XP_011532399.1:p.Asp2049=
XM_011534098.1:c.6147C= XP_011532400.1:p.Asp2049=
XM_011534099.1:c.5772C= XP_011532401.1:p.Asp1924=
XM_011534100.1:c.6579C= XP_011532402.1:p.Asp2193=
XM_005265448.3:c.6384C= XP_005265505.1:p.Asp2128=
XM_011534094.2:c.6684C= XP_011532396.1:p.Asp2228=
XM_011534096.2:c.6495C= XP_011532398.1:p.Asp2165=
XM_011534097.2:c.6147C= XP_011532399.1:p.Asp2049=
XM_011534099.2:c.5772C= XP_011532401.1:p.Asp1924=
XM_011534100.2:c.6579C= XP_011532402.1:p.Asp2193=
XM_017007137.1:c.6684C= XP_016862626.1:p.Asp2228=
XM_017007138.1:c.6681C= XP_016862627.1:p.Asp2227=
XM_017007139.1:c.6657C= XP_016862628.1:p.Asp2219=
XM_017007140.1:c.6624C= XP_016862629.1:p.Asp2208=
XM_017007141.1:c.6624C= XP_016862630.1:p.Asp2208=
XM_017007142.1:c.6600C= XP_016862631.1:p.Asp2200=
XM_017007143.1:c.6600C= XP_016862632.1:p.Asp2200=
XM_017007144.1:c.6600C= XP_016862633.1:p.Asp2200=
XM_017007145.1:c.6555C= XP_016862634.1:p.Asp2185=
NM_001128840.3:c.6429C= MANE Select NP_001122312.1:p.Asp2143=
NM_000720.4:c.6489C= MANE Plus Clinical NP_000711.1:p.Asp2163=
NM_001128839.3:c.6357C= NP_001122311.1:p.Asp2119=