Canonical Allele Identifier: CA908255373
Gene: CACNA1D HGNC NCBI
CHDH HGNC NCBI

Linked Data

dbSNP Id: rs1325822581

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53813308_53813310dup , CM000665.2:g.53813308_53813310dup GRCh38
NC_000003.11:g.53847335_53847337dup , CM000665.1:g.53847335_53847337dup GRCh37
NC_000003.10:g.53822375_53822377dup NCBI36
NG_032999.1:g.323260_323262dup

Transcript Alleles

HGVS Amino-acid change
ENST00000636581.2:n.3777_3779dup (CACNA1D)
ENST00000636633.2:n.5387_5389dup (CACNA1D)
ENST00000636999.2:n.3823_3825dup (CACNA1D)
ENST00000288139.11:c.*1902_*1904dup (CACNA1D) MANE Plus Clinical ENSP00000288139.3:n.*1902_*1904dup
ENST00000315251.11:c.*4467_*4469dup (CHDH) MANE Select ENSP00000319851.5:n.*4467_*4469dup
ENST00000350061.11:c.*1902_*1904dup (CACNA1D) MANE Select ENSP00000288133.5:n.*1902_*1904dup
ENST00000636999.1:n.3815_3817dup (CACNA1D)
ENST00000288139.8:c.*1902_*1904dup (CACNA1D) ENSP00000288139.3:n.*1902_*1904dup
ENST00000315251.10:c.*4467_*4469dup (CHDH) ENSP00000319851.5:n.*4467_*4469dup
XM_006713250.4:c.*4467_*4469dup (CHDH) XP_006713313.1:n.*4467_*4469dup
XM_006713251.4:c.*4467_*4469dup (CHDH) XP_006713314.1:n.*4467_*4469dup
XM_006713252.4:c.*4879_*4881dup (CHDH) XP_006713315.1:n.*4879_*4881dup
XM_011533938.3:c.*4467_*4469dup (CHDH) XP_011532240.1:n.*4467_*4469dup
XM_011533939.3:c.*4467_*4469dup (CHDH) XP_011532241.1:n.*4467_*4469dup
XM_017006797.2:c.*4467_*4469dup (CHDH) XP_016862286.1:n.*4467_*4469dup
XM_017006798.2:c.*4467_*4469dup (CHDH) XP_016862287.1:n.*4467_*4469dup
XM_017006799.2:c.*4879_*4881dup (CHDH) XP_016862288.1:n.*4879_*4881dup
XR_002959545.1:n.4351-255_4351-253dup (CHDH)
NM_001128840.3:c.*1902_*1904dup (CACNA1D) MANE Select NP_001122312.1:n.*1902_*1904dup
NM_018397.5:c.*4467_*4469dup (CHDH) MANE Select NP_060867.2:n.*4467_*4469dup
NM_000720.4:c.*1902_*1904dup (CACNA1D) MANE Plus Clinical NP_000711.1:n.*1902_*1904dup
NM_001128839.3:c.*1902_*1904dup (CACNA1D) NP_001122311.1:n.*1902_*1904dup