Canonical Allele Identifier: CA433896146

Gene: CACNA1D

Linked Data

• MyVariant Identifiers: chr3:g.53835297C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801270C>T , CM000665.2:g.53801270C>T	GRCh38
NC_000003.11:g.53835297C>T , CM000665.1:g.53835297C>T	GRCh37
NC_000003.10:g.53810337C>T	NCBI36
NG_032999.1:g.311222C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5313C>T	ENSP00000418014.2:p.Pro1771=
ENST00000636633.2:n.2252C>T
ENST00000636999.2:n.688C>T
ENST00000288139.11:c.5313C>T MANE Plus Clinical	ENSP00000288139.3:p.Pro1771=
ENST00000350061.11:c.5253C>T MANE Select	ENSP00000288133.5:p.Pro1751=
ENST00000422281.7:c.5208C>T	ENSP00000409174.2:p.Pro1736=
ENST00000636448.1:c.1374C>T
ENST00000636570.1:c.5208C>T	ENSP00000490183.1:p.Pro1736=
ENST00000636629.1:n.609C>T
ENST00000636633.1:n.2252C>T
ENST00000636999.1:n.680C>T
ENST00000637424.1:c.5280C>T	ENSP00000489769.1:p.Pro1760=
ENST00000637844.1:n.7C>T
ENST00000288139.8:c.5313C>T	ENSP00000288139.3:p.Pro1771=
ENST00000350061.9:c.5253C>T	ENSP00000288133.5:p.Pro1751=
ENST00000422281.6:c.5208C>T	ENSP00000409174.2:p.Pro1736=
ENST00000481478.1:c.4332C>T	ENSP00000418014.1:p.Pro1444=
NM_000720.3:c.5313C>T	NP_000711.1:p.Pro1771=
NM_001128839.2:c.5208C>T	NP_001122311.1:p.Pro1736=
NM_001128840.2:c.5253C>T	NP_001122312.1:p.Pro1751=
XM_005265448.2:c.5208C>T	XP_005265505.1:p.Pro1736=
XM_011534094.1:c.5508C>T	XP_011532396.1:p.Pro1836=
XM_011534095.1:c.5397C>T	XP_011532397.1:p.Pro1799=
XM_011534096.1:c.5319C>T	XP_011532398.1:p.Pro1773=
XM_011534097.1:c.4971C>T	XP_011532399.1:p.Pro1657=
XM_011534098.1:c.4971C>T	XP_011532400.1:p.Pro1657=
XM_011534099.1:c.4596C>T	XP_011532401.1:p.Pro1532=
XM_011534100.1:c.5403C>T	XP_011532402.1:p.Pro1801=
XM_005265448.3:c.5208C>T	XP_005265505.1:p.Pro1736=
XM_011534094.2:c.5508C>T	XP_011532396.1:p.Pro1836=
XM_011534096.2:c.5319C>T	XP_011532398.1:p.Pro1773=
XM_011534097.2:c.4971C>T	XP_011532399.1:p.Pro1657=
XM_011534099.2:c.4596C>T	XP_011532401.1:p.Pro1532=
XM_011534100.2:c.5403C>T	XP_011532402.1:p.Pro1801=
XM_017007137.1:c.5508C>T	XP_016862626.1:p.Pro1836=
XM_017007138.1:c.5505C>T	XP_016862627.1:p.Pro1835=
XM_017007139.1:c.5508C>T	XP_016862628.1:p.Pro1836=
XM_017007140.1:c.5448C>T	XP_016862629.1:p.Pro1816=
XM_017007141.1:c.5448C>T	XP_016862630.1:p.Pro1816=
XM_017007142.1:c.5424C>T	XP_016862631.1:p.Pro1808=
XM_017007143.1:c.5424C>T	XP_016862632.1:p.Pro1808=
XM_017007144.1:c.5424C>T	XP_016862633.1:p.Pro1808=
XM_017007145.1:c.5379C>T	XP_016862634.1:p.Pro1793=
NM_001128840.3:c.5253C>T MANE Select	NP_001122312.1:p.Pro1751=
NM_000720.4:c.5313C>T MANE Plus Clinical	NP_000711.1:p.Pro1771=
NM_001128839.3:c.5208C>T	NP_001122311.1:p.Pro1736=