Canonical Allele Identifier: CA353251806

Gene: CACNA1D

Linked Data

• COSMIC: COSM1047315 ; COSM1593926
• MyVariant Identifiers: chr3:g.53835434G>T (hg19) ; chr3:g.53801407G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801407G>T , CM000665.2:g.53801407G>T	GRCh38
NC_000003.11:g.53835434G>T , CM000665.1:g.53835434G>T	GRCh37
NC_000003.10:g.53810474G>T	NCBI36
NG_032999.1:g.311359G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5450G>T	ENSP00000418014.2:p.Arg1817Ile
ENST00000636633.2:n.2389G>T
ENST00000636999.2:n.825G>T
ENST00000288139.11:c.5450G>T MANE Plus Clinical	ENSP00000288139.3:p.Arg1817Ile
ENST00000350061.11:c.5390G>T MANE Select	ENSP00000288133.5:p.Arg1797Ile
ENST00000422281.7:c.5345G>T	ENSP00000409174.2:p.Arg1782Ile
ENST00000636448.1:c.1511G>T
ENST00000636570.1:c.5345G>T	ENSP00000490183.1:p.Arg1782Ile
ENST00000636629.1:n.746G>T
ENST00000636633.1:n.2389G>T
ENST00000636999.1:n.817G>T
ENST00000637424.1:c.5417G>T	ENSP00000489769.1:p.Arg1806Ile
ENST00000637844.1:n.144G>T
ENST00000288139.8:c.5450G>T	ENSP00000288139.3:p.Arg1817Ile
ENST00000350061.9:c.5390G>T	ENSP00000288133.5:p.Arg1797Ile
ENST00000422281.6:c.5345G>T	ENSP00000409174.2:p.Arg1782Ile
ENST00000481478.1:c.4469G>T	ENSP00000418014.1:p.Arg1490Ile
NM_000720.3:c.5450G>T	NP_000711.1:p.Arg1817Ile
NM_001128839.2:c.5345G>T	NP_001122311.1:p.Arg1782Ile
NM_001128840.2:c.5390G>T	NP_001122312.1:p.Arg1797Ile
XM_005265448.2:c.5345G>T	XP_005265505.1:p.Arg1782Ile
XM_011534094.1:c.5645G>T	XP_011532396.1:p.Arg1882Ile
XM_011534095.1:c.5534G>T	XP_011532397.1:p.Arg1845Ile
XM_011534096.1:c.5456G>T	XP_011532398.1:p.Arg1819Ile
XM_011534097.1:c.5108G>T	XP_011532399.1:p.Arg1703Ile
XM_011534098.1:c.5108G>T	XP_011532400.1:p.Arg1703Ile
XM_011534099.1:c.4733G>T	XP_011532401.1:p.Arg1578Ile
XM_011534100.1:c.5540G>T	XP_011532402.1:p.Arg1847Ile
XM_005265448.3:c.5345G>T	XP_005265505.1:p.Arg1782Ile
XM_011534094.2:c.5645G>T	XP_011532396.1:p.Arg1882Ile
XM_011534096.2:c.5456G>T	XP_011532398.1:p.Arg1819Ile
XM_011534097.2:c.5108G>T	XP_011532399.1:p.Arg1703Ile
XM_011534099.2:c.4733G>T	XP_011532401.1:p.Arg1578Ile
XM_011534100.2:c.5540G>T	XP_011532402.1:p.Arg1847Ile
XM_017007137.1:c.5645G>T	XP_016862626.1:p.Arg1882Ile
XM_017007138.1:c.5642G>T	XP_016862627.1:p.Arg1881Ile
XM_017007139.1:c.5645G>T	XP_016862628.1:p.Arg1882Ile
XM_017007140.1:c.5585G>T	XP_016862629.1:p.Arg1862Ile
XM_017007141.1:c.5585G>T	XP_016862630.1:p.Arg1862Ile
XM_017007142.1:c.5561G>T	XP_016862631.1:p.Arg1854Ile
XM_017007143.1:c.5561G>T	XP_016862632.1:p.Arg1854Ile
XM_017007144.1:c.5561G>T	XP_016862633.1:p.Arg1854Ile
XM_017007145.1:c.5516G>T	XP_016862634.1:p.Arg1839Ile
NM_001128840.3:c.5390G>T MANE Select	NP_001122312.1:p.Arg1797Ile
NM_000720.4:c.5450G>T MANE Plus Clinical	NP_000711.1:p.Arg1817Ile
NM_001128839.3:c.5345G>T	NP_001122311.1:p.Arg1782Ile