Canonical Allele Identifier: CA2455109

Gene: CACNA1D

Linked Data

• ClinVar Variation Id: 1381677
• ClinVar RCV Id: RCV001922028
• dbSNP Id: rs555675934
• ExAC: 3:53835421 C / T
• gnomAD v2: 3-53835421-C-T
• gnomAD v3: 3-53801394-C-T
• gnomAD v4: 3-53801394-C-T
• MyVariant Identifiers: chr3:g.53835421C>T (hg19) ; chr3:g.53801394C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801394C>T , CM000665.2:g.53801394C>T	GRCh38
NC_000003.11:g.53835421C>T , CM000665.1:g.53835421C>T	GRCh37
NC_000003.10:g.53810461C>T	NCBI36
NG_032999.1:g.311346C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5437C>T	ENSP00000418014.2:p.Arg1813Trp
ENST00000636633.2:n.2376C>T
ENST00000636999.2:n.812C>T
ENST00000288139.11:c.5437C>T MANE Plus Clinical	ENSP00000288139.3:p.Arg1813Trp
ENST00000350061.11:c.5377C>T MANE Select	ENSP00000288133.5:p.Arg1793Trp
ENST00000422281.7:c.5332C>T	ENSP00000409174.2:p.Arg1778Trp
ENST00000636448.1:c.1498C>T
ENST00000636570.1:c.5332C>T	ENSP00000490183.1:p.Arg1778Trp
ENST00000636629.1:n.733C>T
ENST00000636633.1:n.2376C>T
ENST00000636999.1:n.804C>T
ENST00000637424.1:c.5404C>T	ENSP00000489769.1:p.Arg1802Trp
ENST00000637844.1:n.131C>T
ENST00000288139.8:c.5437C>T	ENSP00000288139.3:p.Arg1813Trp
ENST00000350061.9:c.5377C>T	ENSP00000288133.5:p.Arg1793Trp
ENST00000422281.6:c.5332C>T	ENSP00000409174.2:p.Arg1778Trp
ENST00000481478.1:c.4456C>T	ENSP00000418014.1:p.Arg1486Trp
NM_000720.3:c.5437C>T	NP_000711.1:p.Arg1813Trp
NM_001128839.2:c.5332C>T	NP_001122311.1:p.Arg1778Trp
NM_001128840.2:c.5377C>T	NP_001122312.1:p.Arg1793Trp
XM_005265448.2:c.5332C>T	XP_005265505.1:p.Arg1778Trp
XM_011534094.1:c.5632C>T	XP_011532396.1:p.Arg1878Trp
XM_011534095.1:c.5521C>T	XP_011532397.1:p.Arg1841Trp
XM_011534096.1:c.5443C>T	XP_011532398.1:p.Arg1815Trp
XM_011534097.1:c.5095C>T	XP_011532399.1:p.Arg1699Trp
XM_011534098.1:c.5095C>T	XP_011532400.1:p.Arg1699Trp
XM_011534099.1:c.4720C>T	XP_011532401.1:p.Arg1574Trp
XM_011534100.1:c.5527C>T	XP_011532402.1:p.Arg1843Trp
XM_005265448.3:c.5332C>T	XP_005265505.1:p.Arg1778Trp
XM_011534094.2:c.5632C>T	XP_011532396.1:p.Arg1878Trp
XM_011534096.2:c.5443C>T	XP_011532398.1:p.Arg1815Trp
XM_011534097.2:c.5095C>T	XP_011532399.1:p.Arg1699Trp
XM_011534099.2:c.4720C>T	XP_011532401.1:p.Arg1574Trp
XM_011534100.2:c.5527C>T	XP_011532402.1:p.Arg1843Trp
XM_017007137.1:c.5632C>T	XP_016862626.1:p.Arg1878Trp
XM_017007138.1:c.5629C>T	XP_016862627.1:p.Arg1877Trp
XM_017007139.1:c.5632C>T	XP_016862628.1:p.Arg1878Trp
XM_017007140.1:c.5572C>T	XP_016862629.1:p.Arg1858Trp
XM_017007141.1:c.5572C>T	XP_016862630.1:p.Arg1858Trp
XM_017007142.1:c.5548C>T	XP_016862631.1:p.Arg1850Trp
XM_017007143.1:c.5548C>T	XP_016862632.1:p.Arg1850Trp
XM_017007144.1:c.5548C>T	XP_016862633.1:p.Arg1850Trp
XM_017007145.1:c.5503C>T	XP_016862634.1:p.Arg1835Trp
NM_001128840.3:c.5377C>T MANE Select	NP_001122312.1:p.Arg1793Trp
NM_000720.4:c.5437C>T MANE Plus Clinical	NP_000711.1:p.Arg1813Trp
NM_001128839.3:c.5332C>T	NP_001122311.1:p.Arg1778Trp