Canonical Allele Identifier: CA2616918823
Gene: ACAD8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134262753_134262755del , CM000673.2:g.134262753_134262755del GRCh38
NC_000011.9:g.134132647_134132649del , CM000673.1:g.134132647_134132649del GRCh37
NC_000011.8:g.133637857_133637859del NCBI36
NG_015842.1:g.14214_14216del , LRG_448:g.14214_14216del

Transcript Alleles

HGVS Amino-acid Change
ENST00000281182.9:c.1195+131_1195+133del MANE Select ENSP00000281182.5:n.1195+131_1195+133del
ENST00000281182.8:c.1195+131_1195+133del ENSP00000281182.4:n.1195+131_1195+133del
ENST00000374752.6:c.814+131_814+133del ENSP00000363884.4:n.814+131_814+133del
ENST00000524502.2:n.196-17_196-15del
ENST00000526026.5:c.*885-17_*885-15del ENSP00000431532.1:n.*885-17_*885-15del
ENST00000531338.5:n.1570_1572del
ENST00000533387.5:n.2254+131_2254+133del
NM_014384.2:c.1195+131_1195+133del , LRG_448t1:c.1195+131_1195+133del NP_055199.1:n.1195+131_1195+133del
XM_005271501.2:c.1196-17_1196-15del XP_005271558.1:n.1196-17_1196-15del
XM_011542750.1:c.1195+131_1195+133del XP_011541052.1:n.1195+131_1195+133del
XR_947819.1:n.1259+131_1259+133del
XR_947820.1:n.1778_1780del
XR_947822.1:n.1089+131_1089+133del
XR_947823.1:n.1245+131_1245+133del
XM_005271505.4:c.*1460+131_*1460+133del XP_005271562.1:n.*1460+131_*1460+133del
XM_011542750.3:c.1195+131_1195+133del XP_011541052.1:n.1195+131_1195+133del
XM_017017542.2:c.1195+131_1195+133del XP_016873031.1:n.1195+131_1195+133del
XM_017017543.2:c.1196-17_1196-15del XP_016873032.1:n.1196-17_1196-15del
XM_017017544.2:c.*164+131_*164+133del XP_016873033.1:n.*164+131_*164+133del
XM_017017545.2:c.*538_*540del XP_016873034.1:n.*538_*540del
XM_017017546.2:c.901+131_901+133del XP_016873035.1:n.901+131_901+133del
XM_017017547.2:c.901+131_901+133del XP_016873036.1:n.901+131_901+133del
XM_017017548.2:c.*1832-17_*1832-15del XP_016873037.1:n.*1832-17_*1832-15del
XM_017017549.2:c.*1605+131_*1605+133del XP_016873038.1:n.*1605+131_*1605+133del
XM_024448437.1:c.*473_*475del XP_024304205.1:n.*473_*475del
XM_024448438.1:c.814+131_814+133del XP_024304206.1:n.814+131_814+133del
NM_014384.3:c.1195+131_1195+133del MANE Select NP_055199.1:n.1195+131_1195+133del