Canonical Allele Identifier: CA353249968

Gene: CACNA1D

Linked Data

• MyVariant Identifiers: chr3:g.53835160A>T (hg19) ; chr3:g.53801133A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801133A>T , CM000665.2:g.53801133A>T	GRCh38
NC_000003.11:g.53835160A>T , CM000665.1:g.53835160A>T	GRCh37
NC_000003.10:g.53810200A>T	NCBI36
NG_032999.1:g.311085A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5176A>T	ENSP00000418014.2:p.Thr1726Ser
ENST00000636633.2:n.2194-79A>T
ENST00000636999.2:n.551A>T
ENST00000288139.11:c.5176A>T MANE Plus Clinical	ENSP00000288139.3:p.Thr1726Ser
ENST00000350061.11:c.5116A>T MANE Select	ENSP00000288133.5:p.Thr1706Ser
ENST00000422281.7:c.5071A>T	ENSP00000409174.2:p.Thr1691Ser
ENST00000636448.1:c.1316-79A>T
ENST00000636570.1:c.5071A>T	ENSP00000490183.1:p.Thr1691Ser
ENST00000636629.1:n.472A>T
ENST00000636633.1:n.2194-79A>T
ENST00000636999.1:n.543A>T
ENST00000637424.1:c.5143A>T	ENSP00000489769.1:p.Thr1715Ser
ENST00000288139.8:c.5176A>T	ENSP00000288139.3:p.Thr1726Ser
ENST00000350061.9:c.5116A>T	ENSP00000288133.5:p.Thr1706Ser
ENST00000422281.6:c.5071A>T	ENSP00000409174.2:p.Thr1691Ser
ENST00000481478.1:c.4195A>T	ENSP00000418014.1:p.Thr1399Ser
NM_000720.3:c.5176A>T	NP_000711.1:p.Thr1726Ser
NM_001128839.2:c.5071A>T	NP_001122311.1:p.Thr1691Ser
NM_001128840.2:c.5116A>T	NP_001122312.1:p.Thr1706Ser
XM_005265448.2:c.5071A>T	XP_005265505.1:p.Thr1691Ser
XM_011534094.1:c.5371A>T	XP_011532396.1:p.Thr1791Ser
XM_011534095.1:c.5260A>T	XP_011532397.1:p.Thr1754Ser
XM_011534096.1:c.5182A>T	XP_011532398.1:p.Thr1728Ser
XM_011534097.1:c.4834A>T	XP_011532399.1:p.Thr1612Ser
XM_011534098.1:c.4834A>T	XP_011532400.1:p.Thr1612Ser
XM_011534099.1:c.4459A>T	XP_011532401.1:p.Thr1487Ser
XM_011534100.1:c.5266A>T	XP_011532402.1:p.Thr1756Ser
XM_005265448.3:c.5071A>T	XP_005265505.1:p.Thr1691Ser
XM_011534094.2:c.5371A>T	XP_011532396.1:p.Thr1791Ser
XM_011534096.2:c.5182A>T	XP_011532398.1:p.Thr1728Ser
XM_011534097.2:c.4834A>T	XP_011532399.1:p.Thr1612Ser
XM_011534099.2:c.4459A>T	XP_011532401.1:p.Thr1487Ser
XM_011534100.2:c.5266A>T	XP_011532402.1:p.Thr1756Ser
XM_017007137.1:c.5371A>T	XP_016862626.1:p.Thr1791Ser
XM_017007138.1:c.5368A>T	XP_016862627.1:p.Thr1790Ser
XM_017007139.1:c.5371A>T	XP_016862628.1:p.Thr1791Ser
XM_017007140.1:c.5311A>T	XP_016862629.1:p.Thr1771Ser
XM_017007141.1:c.5311A>T	XP_016862630.1:p.Thr1771Ser
XM_017007142.1:c.5287A>T	XP_016862631.1:p.Thr1763Ser
XM_017007143.1:c.5287A>T	XP_016862632.1:p.Thr1763Ser
XM_017007144.1:c.5287A>T	XP_016862633.1:p.Thr1763Ser
XM_017007145.1:c.5242A>T	XP_016862634.1:p.Thr1748Ser
NM_001128840.3:c.5116A>T MANE Select	NP_001122312.1:p.Thr1706Ser
NM_000720.4:c.5176A>T MANE Plus Clinical	NP_000711.1:p.Thr1726Ser
NM_001128839.3:c.5071A>T	NP_001122311.1:p.Thr1691Ser