Canonical Allele Identifier: CA353250671

Gene: CACNA1D

Linked Data

• MyVariant Identifiers: chr3:g.53835269A>C (hg19) ; chr3:g.53801242A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801242A>C , CM000665.2:g.53801242A>C	GRCh38
NC_000003.11:g.53835269A>C , CM000665.1:g.53835269A>C	GRCh37
NC_000003.10:g.53810309A>C	NCBI36
NG_032999.1:g.311194A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5285A>C	ENSP00000418014.2:p.Asn1762Thr
ENST00000636633.2:n.2224A>C
ENST00000636999.2:n.660A>C
ENST00000288139.11:c.5285A>C MANE Plus Clinical	ENSP00000288139.3:p.Asn1762Thr
ENST00000350061.11:c.5225A>C MANE Select	ENSP00000288133.5:p.Asn1742Thr
ENST00000422281.7:c.5180A>C	ENSP00000409174.2:p.Asn1727Thr
ENST00000636448.1:c.1346A>C
ENST00000636570.1:c.5180A>C	ENSP00000490183.1:p.Asn1727Thr
ENST00000636629.1:n.581A>C
ENST00000636633.1:n.2224A>C
ENST00000636999.1:n.652A>C
ENST00000637424.1:c.5252A>C	ENSP00000489769.1:p.Asn1751Thr
ENST00000288139.8:c.5285A>C	ENSP00000288139.3:p.Asn1762Thr
ENST00000350061.9:c.5225A>C	ENSP00000288133.5:p.Asn1742Thr
ENST00000422281.6:c.5180A>C	ENSP00000409174.2:p.Asn1727Thr
ENST00000481478.1:c.4304A>C	ENSP00000418014.1:p.Asn1435Thr
NM_000720.3:c.5285A>C	NP_000711.1:p.Asn1762Thr
NM_001128839.2:c.5180A>C	NP_001122311.1:p.Asn1727Thr
NM_001128840.2:c.5225A>C	NP_001122312.1:p.Asn1742Thr
XM_005265448.2:c.5180A>C	XP_005265505.1:p.Asn1727Thr
XM_011534094.1:c.5480A>C	XP_011532396.1:p.Asn1827Thr
XM_011534095.1:c.5369A>C	XP_011532397.1:p.Asn1790Thr
XM_011534096.1:c.5291A>C	XP_011532398.1:p.Asn1764Thr
XM_011534097.1:c.4943A>C	XP_011532399.1:p.Asn1648Thr
XM_011534098.1:c.4943A>C	XP_011532400.1:p.Asn1648Thr
XM_011534099.1:c.4568A>C	XP_011532401.1:p.Asn1523Thr
XM_011534100.1:c.5375A>C	XP_011532402.1:p.Asn1792Thr
XM_005265448.3:c.5180A>C	XP_005265505.1:p.Asn1727Thr
XM_011534094.2:c.5480A>C	XP_011532396.1:p.Asn1827Thr
XM_011534096.2:c.5291A>C	XP_011532398.1:p.Asn1764Thr
XM_011534097.2:c.4943A>C	XP_011532399.1:p.Asn1648Thr
XM_011534099.2:c.4568A>C	XP_011532401.1:p.Asn1523Thr
XM_011534100.2:c.5375A>C	XP_011532402.1:p.Asn1792Thr
XM_017007137.1:c.5480A>C	XP_016862626.1:p.Asn1827Thr
XM_017007138.1:c.5477A>C	XP_016862627.1:p.Asn1826Thr
XM_017007139.1:c.5480A>C	XP_016862628.1:p.Asn1827Thr
XM_017007140.1:c.5420A>C	XP_016862629.1:p.Asn1807Thr
XM_017007141.1:c.5420A>C	XP_016862630.1:p.Asn1807Thr
XM_017007142.1:c.5396A>C	XP_016862631.1:p.Asn1799Thr
XM_017007143.1:c.5396A>C	XP_016862632.1:p.Asn1799Thr
XM_017007144.1:c.5396A>C	XP_016862633.1:p.Asn1799Thr
XM_017007145.1:c.5351A>C	XP_016862634.1:p.Asn1784Thr
NM_001128840.3:c.5225A>C MANE Select	NP_001122312.1:p.Asn1742Thr
NM_000720.4:c.5285A>C MANE Plus Clinical	NP_000711.1:p.Asn1762Thr
NM_001128839.3:c.5180A>C	NP_001122311.1:p.Asn1727Thr