Canonical Allele Identifier: CA1365465427

Gene: CACNA1D

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53758384C>A , CM000665.2:g.53758384C>A	GRCh38
NC_000003.11:g.53792411C>A , CM000665.1:g.53792411C>A	GRCh37
NC_000003.10:g.53767451C>A	NCBI36
NG_032999.1:g.268336C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.3847-4167C>A	ENSP00000418014.2:n.3847-4167C>A
ENST00000636627.2:c.3847-4167C>A	ENSP00000490889.2:n.3847-4167C>A
ENST00000288139.11:c.3847-3614C>A MANE Plus Clinical	ENSP00000288139.3:n.3847-3614C>A
ENST00000350061.11:c.3787-3614C>A MANE Select	ENSP00000288133.5:n.3787-3614C>A
ENST00000422281.7:c.3787-3614C>A	ENSP00000409174.2:n.3787-3614C>A
ENST00000636448.1:c.62-4167C>A
ENST00000636570.1:c.3787-3614C>A	ENSP00000490183.1:n.3787-3614C>A
ENST00000636627.1:c.3087-4167C>A
ENST00000636723.1:c.667+4702C>A
ENST00000636938.1:c.3787-3614C>A	ENSP00000490039.1:n.3787-3614C>A
ENST00000637081.1:n.32-3614C>A
ENST00000637424.1:c.3859-3614C>A	ENSP00000489769.1:n.3859-3614C>A
ENST00000638120.1:c.361-3614C>A	ENSP00000489790.1:n.361-3614C>A
ENST00000638129.1:c.366+4702C>A	ENSP00000490523.1:n.366+4702C>A
ENST00000640483.1:c.3820-4167C>A	ENSP00000491921.1:n.3820-4167C>A
ENST00000645528.2:c.975-4167C>A
ENST00000288139.8:c.3847-3614C>A	ENSP00000288139.3:n.3847-3614C>A
ENST00000350061.9:c.3787-3614C>A	ENSP00000288133.5:n.3787-3614C>A
ENST00000422281.6:c.3787-3614C>A	ENSP00000409174.2:n.3787-3614C>A
ENST00000481478.1:c.2866-4167C>A	ENSP00000418014.1:n.2866-4167C>A
NM_000720.3:c.3847-3614C>A	NP_000711.1:n.3847-3614C>A
NM_001128839.2:c.3787-3614C>A	NP_001122311.1:n.3787-3614C>A
NM_001128840.2:c.3787-3614C>A	NP_001122312.1:n.3787-3614C>A
XM_005265448.2:c.3787-3614C>A	XP_005265505.1:n.3787-3614C>A
XM_011534094.1:c.3958-3614C>A	XP_011532396.1:n.3958-3614C>A
XM_011534095.1:c.3847-3614C>A	XP_011532397.1:n.3847-3614C>A
XM_011534096.1:c.3898-3614C>A	XP_011532398.1:n.3898-3614C>A
XM_011534097.1:c.3421-3614C>A	XP_011532399.1:n.3421-3614C>A
XM_011534098.1:c.3421-3614C>A	XP_011532400.1:n.3421-3614C>A
XM_011534099.1:c.3046-3614C>A	XP_011532401.1:n.3046-3614C>A
XM_011534100.1:c.3898-3614C>A	XP_011532402.1:n.3898-3614C>A
XM_005265448.3:c.3787-3614C>A	XP_005265505.1:n.3787-3614C>A
XM_011534094.2:c.3958-3614C>A	XP_011532396.1:n.3958-3614C>A
XM_011534096.2:c.3898-3614C>A	XP_011532398.1:n.3898-3614C>A
XM_011534097.2:c.3421-3614C>A	XP_011532399.1:n.3421-3614C>A
XM_011534099.2:c.3046-3614C>A	XP_011532401.1:n.3046-3614C>A
XM_011534100.2:c.3898-3614C>A	XP_011532402.1:n.3898-3614C>A
XM_017007137.1:c.3958-3614C>A	XP_016862626.1:n.3958-3614C>A
XM_017007138.1:c.3955-3614C>A	XP_016862627.1:n.3955-3614C>A
XM_017007139.1:c.3958-3614C>A	XP_016862628.1:n.3958-3614C>A
XM_017007140.1:c.3898-3614C>A	XP_016862629.1:n.3898-3614C>A
XM_017007141.1:c.3898-3614C>A	XP_016862630.1:n.3898-3614C>A
XM_017007142.1:c.3958-3614C>A	XP_016862631.1:n.3958-3614C>A
XM_017007143.1:c.3958-4167C>A	XP_016862632.1:n.3958-4167C>A
XM_017007144.1:c.3958-4167C>A	XP_016862633.1:n.3958-4167C>A
XM_017007145.1:c.3958-3614C>A	XP_016862634.1:n.3958-3614C>A
NM_001128840.3:c.3787-3614C>A MANE Select	NP_001122312.1:n.3787-3614C>A
NM_000720.4:c.3847-3614C>A MANE Plus Clinical	NP_000711.1:n.3847-3614C>A
NM_001128839.3:c.3787-3614C>A	NP_001122311.1:n.3787-3614C>A