Canonical Allele Identifier: CA2794211405

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262934_134262935dup , CM000673.2:g.134262934_134262935dup	GRCh38
NC_000011.9:g.134132828_134132829dup , CM000673.1:g.134132828_134132829dup	GRCh37
NC_000011.8:g.133638038_133638039dup	NCBI36
NG_015842.1:g.14395_14396dup , LRG_448:g.14395_14396dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1195+312_1195+313dup MANE Select	ENSP00000281182.5:n.1195+312_1195+313dup
ENST00000281182.8:c.1195+312_1195+313dup	ENSP00000281182.4:n.1195+312_1195+313dup
ENST00000374752.6:c.814+312_814+313dup	ENSP00000363884.4:n.814+312_814+313dup
ENST00000524502.2:n.360_361dup
ENST00000526026.5:c.*1049_*1050dup	ENSP00000431532.1:n.*1049_*1050dup
ENST00000531338.5:n.1751_1752dup
ENST00000533387.5:n.2254+312_2254+313dup
NM_014384.2:c.1195+312_1195+313dup , LRG_448t1:c.1195+312_1195+313dup	NP_055199.1:n.1195+312_1195+313dup
XM_005271501.2:c.*55_*56dup	XP_005271558.1:n.*55_*56dup
XM_011542750.1:c.1195+312_1195+313dup	XP_011541052.1:n.1195+312_1195+313dup
XR_947819.1:n.1259+312_1259+313dup
XR_947820.1:n.1959_1960dup
XR_947822.1:n.1089+312_1089+313dup
XR_947823.1:n.1245+312_1245+313dup
XM_005271505.4:c.*1460+312_*1460+313dup	XP_005271562.1:n.*1460+312_*1460+313dup
XM_011542750.3:c.1195+312_1195+313dup	XP_011541052.1:n.1195+312_1195+313dup
XM_017017542.2:c.1195+312_1195+313dup	XP_016873031.1:n.1195+312_1195+313dup
XM_017017543.2:c.*55_*56dup	XP_016873032.1:n.*55_*56dup
XM_017017544.2:c.*164+312_*164+313dup	XP_016873033.1:n.*164+312_*164+313dup
XM_017017545.2:c.*719_*720dup	XP_016873034.1:n.*719_*720dup
XM_017017546.2:c.901+312_901+313dup	XP_016873035.1:n.901+312_901+313dup
XM_017017547.2:c.901+312_901+313dup	XP_016873036.1:n.901+312_901+313dup
XM_017017548.2:c.*1996_*1997dup	XP_016873037.1:n.*1996_*1997dup
XM_017017549.2:c.*1605+312_*1605+313dup	XP_016873038.1:n.*1605+312_*1605+313dup
XM_024448437.1:c.*654_*655dup	XP_024304205.1:n.*654_*655dup
XM_024448438.1:c.814+312_814+313dup	XP_024304206.1:n.814+312_814+313dup
NM_014384.3:c.1195+312_1195+313dup MANE Select	NP_055199.1:n.1195+312_1195+313dup