Canonical Allele Identifier: CA2010875257

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262957_134262959delinsCAG , CM000673.2:g.134262957_134262959delinsCAG	GRCh38
NC_000011.9:g.134132851_134132853delinsCAG , CM000673.1:g.134132851_134132853delinsCAG	GRCh37
NC_000011.8:g.133638061_133638063delinsCAG	NCBI36
NG_015842.1:g.14418_14420delinsCAG , LRG_448:g.14418_14420delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1195+335_1195+337delinsCAG MANE Select	ENSP00000281182.5:n.1195+335_1195+337delinsCAG
ENST00000281182.8:c.1195+335_1195+337delinsCAG	ENSP00000281182.4:n.1195+335_1195+337delinsCAG
ENST00000374752.6:c.814+335_814+337delinsCAG	ENSP00000363884.4:n.814+335_814+337delinsCAG
ENST00000524502.2:n.383_385delinsCAG
ENST00000531338.5:n.1774_1776delinsCAG
ENST00000533387.5:n.2254+335_2254+337delinsCAG
NM_014384.2:c.1195+335_1195+337delinsCAG , LRG_448t1:c.1195+335_1195+337delinsCAG	NP_055199.1:n.1195+335_1195+337delinsCAG
XM_005271501.2:c.*78_*80delinsCAG	XP_005271558.1:n.*78_*80delinsCAG
XM_011542750.1:c.1195+335_1195+337delinsCAG	XP_011541052.1:n.1195+335_1195+337delinsCAG
XR_947819.1:n.1259+335_1259+337delinsCAG
XR_947820.1:n.1982_1984delinsCAG
XR_947822.1:n.1089+335_1089+337delinsCAG
XR_947823.1:n.1245+335_1245+337delinsCAG
XM_005271505.4:c.*1460+335_*1460+337delinsCAG	XP_005271562.1:n.*1460+335_*1460+337delinsCAG
XM_011542750.3:c.1195+335_1195+337delinsCAG	XP_011541052.1:n.1195+335_1195+337delinsCAG
XM_017017542.2:c.1195+335_1195+337delinsCAG	XP_016873031.1:n.1195+335_1195+337delinsCAG
XM_017017543.2:c.*78_*80delinsCAG	XP_016873032.1:n.*78_*80delinsCAG
XM_017017544.2:c.*164+335_*164+337delinsCAG	XP_016873033.1:n.*164+335_*164+337delinsCAG
XM_017017545.2:c.*742_*744delinsCAG	XP_016873034.1:n.*742_*744delinsCAG
XM_017017546.2:c.901+335_901+337delinsCAG	XP_016873035.1:n.901+335_901+337delinsCAG
XM_017017547.2:c.901+335_901+337delinsCAG	XP_016873036.1:n.901+335_901+337delinsCAG
XM_017017548.2:c.*2019_*2021delinsCAG	XP_016873037.1:n.*2019_*2021delinsCAG
XM_017017549.2:c.*1605+335_*1605+337delinsCAG	XP_016873038.1:n.*1605+335_*1605+337delinsCAG
XM_024448437.1:c.*677_*679delinsCAG	XP_024304205.1:n.*677_*679delinsCAG
XM_024448438.1:c.814+335_814+337delinsCAG	XP_024304206.1:n.814+335_814+337delinsCAG
NM_014384.3:c.1195+335_1195+337delinsCAG MANE Select	NP_055199.1:n.1195+335_1195+337delinsCAG