Canonical Allele Identifier: CA353383995

Gene: CACNA1D

Linked Data

• MyVariant Identifiers: chr3:g.53707743A>G (hg19) ; chr3:g.53673716A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53673716A>G , CM000665.2:g.53673716A>G	GRCh38
NC_000003.11:g.53707743A>G , CM000665.1:g.53707743A>G	GRCh37
NC_000003.10:g.53682783A>G	NCBI36
NG_032999.1:g.183668A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000481478.2:c.1220+590A>G	ENSP00000418014.2:n.1220+590A>G
ENST00000636627.2:c.1120A>G	ENSP00000490889.2:p.Asn374Asp
ENST00000288139.11:c.1120A>G MANE Plus Clinical	ENSP00000288139.3:p.Asn374Asp
ENST00000350061.11:c.1220+590A>G MANE Select	ENSP00000288133.5:n.1220+590A>G
ENST00000422281.7:c.1220+590A>G	ENSP00000409174.2:n.1220+590A>G
ENST00000498251.2:n.66+590A>G
ENST00000636570.1:c.1120A>G	ENSP00000490183.1:p.Asn374Asp
ENST00000636627.1:c.360A>G
ENST00000636938.1:c.1120A>G	ENSP00000490039.1:p.Asn374Asp
ENST00000637424.1:c.1192A>G	ENSP00000489769.1:p.Asn398Asp
ENST00000640483.1:c.1093A>G	ENSP00000491921.1:p.Asn365Asp
ENST00000288139.8:c.1120A>G	ENSP00000288139.3:p.Asn374Asp
ENST00000350061.9:c.1220+590A>G	ENSP00000288133.5:n.1220+590A>G
ENST00000422281.6:c.1220+590A>G	ENSP00000409174.2:n.1220+590A>G
ENST00000464429.1:n.162A>G
ENST00000481085.5:c.177A>G
ENST00000481478.1:c.239+590A>G	ENSP00000418014.1:n.239+590A>G
ENST00000498251.1:n.66+590A>G
NM_000720.3:c.1120A>G	NP_000711.1:p.Asn374Asp
NM_001128839.2:c.1220+590A>G	NP_001122311.1:n.1220+590A>G
NM_001128840.2:c.1220+590A>G	NP_001122312.1:n.1220+590A>G
XM_005265448.2:c.1120A>G	XP_005265505.1:p.Asn374Asp
XM_011534094.1:c.1331+590A>G	XP_011532396.1:n.1331+590A>G
XM_011534095.1:c.1120A>G	XP_011532397.1:p.Asn374Asp
XM_011534096.1:c.1231A>G	XP_011532398.1:p.Asn411Asp
XM_011534097.1:c.694A>G	XP_011532399.1:p.Asn232Asp
XM_011534098.1:c.694A>G	XP_011532400.1:p.Asn232Asp
XM_011534099.1:c.319A>G	XP_011532401.1:p.Asn107Asp
XM_011534100.1:c.1231A>G	XP_011532402.1:p.Asn411Asp
XM_005265448.3:c.1120A>G	XP_005265505.1:p.Asn374Asp
XM_011534094.2:c.1331+590A>G	XP_011532396.1:n.1331+590A>G
XM_011534096.2:c.1231A>G	XP_011532398.1:p.Asn411Asp
XM_011534097.2:c.694A>G	XP_011532399.1:p.Asn232Asp
XM_011534099.2:c.319A>G	XP_011532401.1:p.Asn107Asp
XM_011534100.2:c.1231A>G	XP_011532402.1:p.Asn411Asp
XM_017007137.1:c.1231A>G	XP_016862626.1:p.Asn411Asp
XM_017007138.1:c.1231A>G	XP_016862627.1:p.Asn411Asp
XM_017007139.1:c.1231A>G	XP_016862628.1:p.Asn411Asp
XM_017007140.1:c.1231A>G	XP_016862629.1:p.Asn411Asp
XM_017007141.1:c.1331+590A>G	XP_016862630.1:n.1331+590A>G
XM_017007142.1:c.1231A>G	XP_016862631.1:p.Asn411Asp
XM_017007143.1:c.1231A>G	XP_016862632.1:p.Asn411Asp
XM_017007144.1:c.1331+590A>G	XP_016862633.1:n.1331+590A>G
XM_017007145.1:c.1231A>G	XP_016862634.1:p.Asn411Asp
NM_001128840.3:c.1220+590A>G MANE Select	NP_001122312.1:n.1220+590A>G
NM_000720.4:c.1120A>G MANE Plus Clinical	NP_000711.1:p.Asn374Asp
NM_001128839.3:c.1220+590A>G	NP_001122311.1:n.1220+590A>G