Canonical Allele Identifier: CA353250889

Gene: CACNA1D

Linked Data

• MyVariant Identifiers: chr3:g.53835316C>G (hg19) ; chr3:g.53801289C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801289C>G , CM000665.2:g.53801289C>G	GRCh38
NC_000003.11:g.53835316C>G , CM000665.1:g.53835316C>G	GRCh37
NC_000003.10:g.53810356C>G	NCBI36
NG_032999.1:g.311241C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5332C>G	ENSP00000418014.2:p.Leu1778Val
ENST00000636633.2:n.2271C>G
ENST00000636999.2:n.707C>G
ENST00000288139.11:c.5332C>G MANE Plus Clinical	ENSP00000288139.3:p.Leu1778Val
ENST00000350061.11:c.5272C>G MANE Select	ENSP00000288133.5:p.Leu1758Val
ENST00000422281.7:c.5227C>G	ENSP00000409174.2:p.Leu1743Val
ENST00000636448.1:c.1393C>G
ENST00000636570.1:c.5227C>G	ENSP00000490183.1:p.Leu1743Val
ENST00000636629.1:n.628C>G
ENST00000636633.1:n.2271C>G
ENST00000636999.1:n.699C>G
ENST00000637424.1:c.5299C>G	ENSP00000489769.1:p.Leu1767Val
ENST00000637844.1:n.26C>G
ENST00000288139.8:c.5332C>G	ENSP00000288139.3:p.Leu1778Val
ENST00000350061.9:c.5272C>G	ENSP00000288133.5:p.Leu1758Val
ENST00000422281.6:c.5227C>G	ENSP00000409174.2:p.Leu1743Val
ENST00000481478.1:c.4351C>G	ENSP00000418014.1:p.Leu1451Val
NM_000720.3:c.5332C>G	NP_000711.1:p.Leu1778Val
NM_001128839.2:c.5227C>G	NP_001122311.1:p.Leu1743Val
NM_001128840.2:c.5272C>G	NP_001122312.1:p.Leu1758Val
XM_005265448.2:c.5227C>G	XP_005265505.1:p.Leu1743Val
XM_011534094.1:c.5527C>G	XP_011532396.1:p.Leu1843Val
XM_011534095.1:c.5416C>G	XP_011532397.1:p.Leu1806Val
XM_011534096.1:c.5338C>G	XP_011532398.1:p.Leu1780Val
XM_011534097.1:c.4990C>G	XP_011532399.1:p.Leu1664Val
XM_011534098.1:c.4990C>G	XP_011532400.1:p.Leu1664Val
XM_011534099.1:c.4615C>G	XP_011532401.1:p.Leu1539Val
XM_011534100.1:c.5422C>G	XP_011532402.1:p.Leu1808Val
XM_005265448.3:c.5227C>G	XP_005265505.1:p.Leu1743Val
XM_011534094.2:c.5527C>G	XP_011532396.1:p.Leu1843Val
XM_011534096.2:c.5338C>G	XP_011532398.1:p.Leu1780Val
XM_011534097.2:c.4990C>G	XP_011532399.1:p.Leu1664Val
XM_011534099.2:c.4615C>G	XP_011532401.1:p.Leu1539Val
XM_011534100.2:c.5422C>G	XP_011532402.1:p.Leu1808Val
XM_017007137.1:c.5527C>G	XP_016862626.1:p.Leu1843Val
XM_017007138.1:c.5524C>G	XP_016862627.1:p.Leu1842Val
XM_017007139.1:c.5527C>G	XP_016862628.1:p.Leu1843Val
XM_017007140.1:c.5467C>G	XP_016862629.1:p.Leu1823Val
XM_017007141.1:c.5467C>G	XP_016862630.1:p.Leu1823Val
XM_017007142.1:c.5443C>G	XP_016862631.1:p.Leu1815Val
XM_017007143.1:c.5443C>G	XP_016862632.1:p.Leu1815Val
XM_017007144.1:c.5443C>G	XP_016862633.1:p.Leu1815Val
XM_017007145.1:c.5398C>G	XP_016862634.1:p.Leu1800Val
NM_001128840.3:c.5272C>G MANE Select	NP_001122312.1:p.Leu1758Val
NM_000720.4:c.5332C>G MANE Plus Clinical	NP_000711.1:p.Leu1778Val
NM_001128839.3:c.5227C>G	NP_001122311.1:p.Leu1743Val