Canonical Allele Identifier: CA1365484254

Gene: CACNA1D

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53801457_53801460delinsTGTG , CM000665.2:g.53801457_53801460delinsTGTG	GRCh38
NC_000003.11:g.53835484_53835487delinsTGTG , CM000665.1:g.53835484_53835487delinsTGTG	GRCh37
NC_000003.10:g.53810524_53810527delinsTGTG	NCBI36
NG_032999.1:g.311409_311412delinsTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481478.2:c.5468+32_5468+35delinsTGTG	ENSP00000418014.2:n.5468+32_5468+35delinsTGTG
ENST00000636633.2:n.2407+32_2407+35delinsTGTG
ENST00000636999.2:n.843+32_843+35delinsTGTG
ENST00000288139.11:c.5468+32_5468+35delinsTGTG MANE Plus Clinical	ENSP00000288139.3:n.5468+32_5468+35delinsTGTG
ENST00000350061.11:c.5408+32_5408+35delinsTGTG MANE Select	ENSP00000288133.5:n.5408+32_5408+35delinsTGTG
ENST00000422281.7:c.5363+32_5363+35delinsTGTG	ENSP00000409174.2:n.5363+32_5363+35delinsTGTG
ENST00000636448.1:c.1529+32_1529+35delinsTGTG
ENST00000636570.1:c.5363+32_5363+35delinsTGTG	ENSP00000490183.1:n.5363+32_5363+35delinsTGTG
ENST00000636629.1:n.764+32_764+35delinsTGTG
ENST00000636633.1:n.2407+32_2407+35delinsTGTG
ENST00000636999.1:n.835+32_835+35delinsTGTG
ENST00000637424.1:c.5435+32_5435+35delinsTGTG	ENSP00000489769.1:n.5435+32_5435+35delinsTGTG
ENST00000637844.1:n.162+32_162+35delinsTGTG
ENST00000288139.8:c.5468+32_5468+35delinsTGTG	ENSP00000288139.3:n.5468+32_5468+35delinsTGTG
ENST00000350061.9:c.5408+32_5408+35delinsTGTG	ENSP00000288133.5:n.5408+32_5408+35delinsTGTG
ENST00000422281.6:c.5363+32_5363+35delinsTGTG	ENSP00000409174.2:n.5363+32_5363+35delinsTGTG
ENST00000481478.1:c.4487+32_4487+35delinsTGTG	ENSP00000418014.1:n.4487+32_4487+35delinsTGTG
NM_000720.3:c.5468+32_5468+35delinsTGTG	NP_000711.1:n.5468+32_5468+35delinsTGTG
NM_001128839.2:c.5363+32_5363+35delinsTGTG	NP_001122311.1:n.5363+32_5363+35delinsTGTG
NM_001128840.2:c.5408+32_5408+35delinsTGTG	NP_001122312.1:n.5408+32_5408+35delinsTGTG
XM_005265448.2:c.5363+32_5363+35delinsTGTG	XP_005265505.1:n.5363+32_5363+35delinsTGTG
XM_011534094.1:c.5663+32_5663+35delinsTGTG	XP_011532396.1:n.5663+32_5663+35delinsTGTG
XM_011534095.1:c.5552+32_5552+35delinsTGTG	XP_011532397.1:n.5552+32_5552+35delinsTGTG
XM_011534096.1:c.5474+32_5474+35delinsTGTG	XP_011532398.1:n.5474+32_5474+35delinsTGTG
XM_011534097.1:c.5126+32_5126+35delinsTGTG	XP_011532399.1:n.5126+32_5126+35delinsTGTG
XM_011534098.1:c.5126+32_5126+35delinsTGTG	XP_011532400.1:n.5126+32_5126+35delinsTGTG
XM_011534099.1:c.4751+32_4751+35delinsTGTG	XP_011532401.1:n.4751+32_4751+35delinsTGTG
XM_011534100.1:c.5558+32_5558+35delinsTGTG	XP_011532402.1:n.5558+32_5558+35delinsTGTG
XM_005265448.3:c.5363+32_5363+35delinsTGTG	XP_005265505.1:n.5363+32_5363+35delinsTGTG
XM_011534094.2:c.5663+32_5663+35delinsTGTG	XP_011532396.1:n.5663+32_5663+35delinsTGTG
XM_011534096.2:c.5474+32_5474+35delinsTGTG	XP_011532398.1:n.5474+32_5474+35delinsTGTG
XM_011534097.2:c.5126+32_5126+35delinsTGTG	XP_011532399.1:n.5126+32_5126+35delinsTGTG
XM_011534099.2:c.4751+32_4751+35delinsTGTG	XP_011532401.1:n.4751+32_4751+35delinsTGTG
XM_011534100.2:c.5558+32_5558+35delinsTGTG	XP_011532402.1:n.5558+32_5558+35delinsTGTG
XM_017007137.1:c.5663+32_5663+35delinsTGTG	XP_016862626.1:n.5663+32_5663+35delinsTGTG
XM_017007138.1:c.5660+32_5660+35delinsTGTG	XP_016862627.1:n.5660+32_5660+35delinsTGTG
XM_017007139.1:c.5663+32_5663+35delinsTGTG	XP_016862628.1:n.5663+32_5663+35delinsTGTG
XM_017007140.1:c.5603+32_5603+35delinsTGTG	XP_016862629.1:n.5603+32_5603+35delinsTGTG
XM_017007141.1:c.5603+32_5603+35delinsTGTG	XP_016862630.1:n.5603+32_5603+35delinsTGTG
XM_017007142.1:c.5579+32_5579+35delinsTGTG	XP_016862631.1:n.5579+32_5579+35delinsTGTG
XM_017007143.1:c.5579+32_5579+35delinsTGTG	XP_016862632.1:n.5579+32_5579+35delinsTGTG
XM_017007144.1:c.5579+32_5579+35delinsTGTG	XP_016862633.1:n.5579+32_5579+35delinsTGTG
XM_017007145.1:c.5534+32_5534+35delinsTGTG	XP_016862634.1:n.5534+32_5534+35delinsTGTG
NM_001128840.3:c.5408+32_5408+35delinsTGTG MANE Select	NP_001122312.1:n.5408+32_5408+35delinsTGTG
NM_000720.4:c.5468+32_5468+35delinsTGTG MANE Plus Clinical	NP_000711.1:n.5468+32_5468+35delinsTGTG
NM_001128839.3:c.5363+32_5363+35delinsTGTG	NP_001122311.1:n.5363+32_5363+35delinsTGTG