Canonical Allele Identifier: CA1365484202

Gene: CACNA1D

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801323G= , CM000665.2:g.53801323G=	GRCh38
NC_000003.11:g.53835350G= , CM000665.1:g.53835350G=	GRCh37
NC_000003.10:g.53810390G=	NCBI36
NG_032999.1:g.311275G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5366G=	ENSP00000418014.2:p.Gly1789=
ENST00000636633.2:n.2305G=
ENST00000636999.2:n.741G=
ENST00000288139.11:c.5366G= MANE Plus Clinical	ENSP00000288139.3:p.Gly1789=
ENST00000350061.11:c.5306G= MANE Select	ENSP00000288133.5:p.Gly1769=
ENST00000422281.7:c.5261G=	ENSP00000409174.2:p.Gly1754=
ENST00000636448.1:c.1427G=
ENST00000636570.1:c.5261G=	ENSP00000490183.1:p.Gly1754=
ENST00000636629.1:n.662G=
ENST00000636633.1:n.2305G=
ENST00000636999.1:n.733G=
ENST00000637424.1:c.5333G=	ENSP00000489769.1:p.Gly1778=
ENST00000637844.1:n.60G=
ENST00000288139.8:c.5366G=	ENSP00000288139.3:p.Gly1789=
ENST00000350061.9:c.5306G=	ENSP00000288133.5:p.Gly1769=
ENST00000422281.6:c.5261G=	ENSP00000409174.2:p.Gly1754=
ENST00000481478.1:c.4385G=	ENSP00000418014.1:p.Gly1462=
NM_000720.3:c.5366G=	NP_000711.1:p.Gly1789=
NM_001128839.2:c.5261G=	NP_001122311.1:p.Gly1754=
NM_001128840.2:c.5306G=	NP_001122312.1:p.Gly1769=
XM_005265448.2:c.5261G=	XP_005265505.1:p.Gly1754=
XM_011534094.1:c.5561G=	XP_011532396.1:p.Gly1854=
XM_011534095.1:c.5450G=	XP_011532397.1:p.Gly1817=
XM_011534096.1:c.5372G=	XP_011532398.1:p.Gly1791=
XM_011534097.1:c.5024G=	XP_011532399.1:p.Gly1675=
XM_011534098.1:c.5024G=	XP_011532400.1:p.Gly1675=
XM_011534099.1:c.4649G=	XP_011532401.1:p.Gly1550=
XM_011534100.1:c.5456G=	XP_011532402.1:p.Gly1819=
XM_005265448.3:c.5261G=	XP_005265505.1:p.Gly1754=
XM_011534094.2:c.5561G=	XP_011532396.1:p.Gly1854=
XM_011534096.2:c.5372G=	XP_011532398.1:p.Gly1791=
XM_011534097.2:c.5024G=	XP_011532399.1:p.Gly1675=
XM_011534099.2:c.4649G=	XP_011532401.1:p.Gly1550=
XM_011534100.2:c.5456G=	XP_011532402.1:p.Gly1819=
XM_017007137.1:c.5561G=	XP_016862626.1:p.Gly1854=
XM_017007138.1:c.5558G=	XP_016862627.1:p.Gly1853=
XM_017007139.1:c.5561G=	XP_016862628.1:p.Gly1854=
XM_017007140.1:c.5501G=	XP_016862629.1:p.Gly1834=
XM_017007141.1:c.5501G=	XP_016862630.1:p.Gly1834=
XM_017007142.1:c.5477G=	XP_016862631.1:p.Gly1826=
XM_017007143.1:c.5477G=	XP_016862632.1:p.Gly1826=
XM_017007144.1:c.5477G=	XP_016862633.1:p.Gly1826=
XM_017007145.1:c.5432G=	XP_016862634.1:p.Gly1811=
NM_001128840.3:c.5306G= MANE Select	NP_001122312.1:p.Gly1769=
NM_000720.4:c.5366G= MANE Plus Clinical	NP_000711.1:p.Gly1789=
NM_001128839.3:c.5261G=	NP_001122311.1:p.Gly1754=