Canonical Allele Identifier: CA908235991

Gene: CACNA1D

Linked Data

• dbSNP Id: rs1276967725
• MyVariant Identifiers: chr3:g.53835481T>A (hg19) ; chr3:g.53801454T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801454T>A , CM000665.2:g.53801454T>A	GRCh38
NC_000003.11:g.53835481T>A , CM000665.1:g.53835481T>A	GRCh37
NC_000003.10:g.53810521T>A	NCBI36
NG_032999.1:g.311406T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5468+29T>A	ENSP00000418014.2:n.5468+29T>A
ENST00000636633.2:n.2407+29T>A
ENST00000636999.2:n.843+29T>A
ENST00000288139.11:c.5468+29T>A MANE Plus Clinical	ENSP00000288139.3:n.5468+29T>A
ENST00000350061.11:c.5408+29T>A MANE Select	ENSP00000288133.5:n.5408+29T>A
ENST00000422281.7:c.5363+29T>A	ENSP00000409174.2:n.5363+29T>A
ENST00000636448.1:c.1529+29T>A
ENST00000636570.1:c.5363+29T>A	ENSP00000490183.1:n.5363+29T>A
ENST00000636629.1:n.764+29T>A
ENST00000636633.1:n.2407+29T>A
ENST00000636999.1:n.835+29T>A
ENST00000637424.1:c.5435+29T>A	ENSP00000489769.1:n.5435+29T>A
ENST00000637844.1:n.162+29T>A
ENST00000288139.8:c.5468+29T>A	ENSP00000288139.3:n.5468+29T>A
ENST00000350061.9:c.5408+29T>A	ENSP00000288133.5:n.5408+29T>A
ENST00000422281.6:c.5363+29T>A	ENSP00000409174.2:n.5363+29T>A
ENST00000481478.1:c.4487+29T>A	ENSP00000418014.1:n.4487+29T>A
NM_000720.3:c.5468+29T>A	NP_000711.1:n.5468+29T>A
NM_001128839.2:c.5363+29T>A	NP_001122311.1:n.5363+29T>A
NM_001128840.2:c.5408+29T>A	NP_001122312.1:n.5408+29T>A
XM_005265448.2:c.5363+29T>A	XP_005265505.1:n.5363+29T>A
XM_011534094.1:c.5663+29T>A	XP_011532396.1:n.5663+29T>A
XM_011534095.1:c.5552+29T>A	XP_011532397.1:n.5552+29T>A
XM_011534096.1:c.5474+29T>A	XP_011532398.1:n.5474+29T>A
XM_011534097.1:c.5126+29T>A	XP_011532399.1:n.5126+29T>A
XM_011534098.1:c.5126+29T>A	XP_011532400.1:n.5126+29T>A
XM_011534099.1:c.4751+29T>A	XP_011532401.1:n.4751+29T>A
XM_011534100.1:c.5558+29T>A	XP_011532402.1:n.5558+29T>A
XM_005265448.3:c.5363+29T>A	XP_005265505.1:n.5363+29T>A
XM_011534094.2:c.5663+29T>A	XP_011532396.1:n.5663+29T>A
XM_011534096.2:c.5474+29T>A	XP_011532398.1:n.5474+29T>A
XM_011534097.2:c.5126+29T>A	XP_011532399.1:n.5126+29T>A
XM_011534099.2:c.4751+29T>A	XP_011532401.1:n.4751+29T>A
XM_011534100.2:c.5558+29T>A	XP_011532402.1:n.5558+29T>A
XM_017007137.1:c.5663+29T>A	XP_016862626.1:n.5663+29T>A
XM_017007138.1:c.5660+29T>A	XP_016862627.1:n.5660+29T>A
XM_017007139.1:c.5663+29T>A	XP_016862628.1:n.5663+29T>A
XM_017007140.1:c.5603+29T>A	XP_016862629.1:n.5603+29T>A
XM_017007141.1:c.5603+29T>A	XP_016862630.1:n.5603+29T>A
XM_017007142.1:c.5579+29T>A	XP_016862631.1:n.5579+29T>A
XM_017007143.1:c.5579+29T>A	XP_016862632.1:n.5579+29T>A
XM_017007144.1:c.5579+29T>A	XP_016862633.1:n.5579+29T>A
XM_017007145.1:c.5534+29T>A	XP_016862634.1:n.5534+29T>A
NM_001128840.3:c.5408+29T>A MANE Select	NP_001122312.1:n.5408+29T>A
NM_000720.4:c.5468+29T>A MANE Plus Clinical	NP_000711.1:n.5468+29T>A
NM_001128839.3:c.5363+29T>A	NP_001122311.1:n.5363+29T>A