Canonical Allele Identifier: CA2010875166

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262887_134262891delinsTAATG , CM000673.2:g.134262887_134262891delinsTAATG	GRCh38
NC_000011.9:g.134132781_134132785delinsTAATG , CM000673.1:g.134132781_134132785delinsTAATG	GRCh37
NC_000011.8:g.133637991_133637995delinsTAATG	NCBI36
NG_015842.1:g.14348_14352delinsTAATG , LRG_448:g.14348_14352delinsTAATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1195+265_1195+269delinsTAATG MANE Select	ENSP00000281182.5:n.1195+265_1195+269delinsTAATG
ENST00000281182.8:c.1195+265_1195+269delinsTAATG	ENSP00000281182.4:n.1195+265_1195+269delinsTAATG
ENST00000374752.6:c.814+265_814+269delinsTAATG	ENSP00000363884.4:n.814+265_814+269delinsTAATG
ENST00000524502.2:n.313_317delinsTAATG
ENST00000526026.5:c.*1002_*1006delinsTAATG	ENSP00000431532.1:n.*1002_*1006delinsTAATG
ENST00000531338.5:n.1704_1708delinsTAATG
ENST00000533387.5:n.2254+265_2254+269delinsTAATG
NM_014384.2:c.1195+265_1195+269delinsTAATG , LRG_448t1:c.1195+265_1195+269delinsTAATG	NP_055199.1:n.1195+265_1195+269delinsTAATG
XM_005271501.2:c.*8_*12delinsTAATG	XP_005271558.1:n.*8_*12delinsTAATG
XM_011542750.1:c.1195+265_1195+269delinsTAATG	XP_011541052.1:n.1195+265_1195+269delinsTAATG
XR_947819.1:n.1259+265_1259+269delinsTAATG
XR_947820.1:n.1912_1916delinsTAATG
XR_947822.1:n.1089+265_1089+269delinsTAATG
XR_947823.1:n.1245+265_1245+269delinsTAATG
XM_005271505.4:c.*1460+265_*1460+269delinsTAATG	XP_005271562.1:n.*1460+265_*1460+269delinsTAATG
XM_011542750.3:c.1195+265_1195+269delinsTAATG	XP_011541052.1:n.1195+265_1195+269delinsTAATG
XM_017017542.2:c.1195+265_1195+269delinsTAATG	XP_016873031.1:n.1195+265_1195+269delinsTAATG
XM_017017543.2:c.*8_*12delinsTAATG	XP_016873032.1:n.*8_*12delinsTAATG
XM_017017544.2:c.*164+265_*164+269delinsTAATG	XP_016873033.1:n.*164+265_*164+269delinsTAATG
XM_017017545.2:c.*672_*676delinsTAATG	XP_016873034.1:n.*672_*676delinsTAATG
XM_017017546.2:c.901+265_901+269delinsTAATG	XP_016873035.1:n.901+265_901+269delinsTAATG
XM_017017547.2:c.901+265_901+269delinsTAATG	XP_016873036.1:n.901+265_901+269delinsTAATG
XM_017017548.2:c.*1949_*1953delinsTAATG	XP_016873037.1:n.*1949_*1953delinsTAATG
XM_017017549.2:c.*1605+265_*1605+269delinsTAATG	XP_016873038.1:n.*1605+265_*1605+269delinsTAATG
XM_024448437.1:c.*607_*611delinsTAATG	XP_024304205.1:n.*607_*611delinsTAATG
XM_024448438.1:c.814+265_814+269delinsTAATG	XP_024304206.1:n.814+265_814+269delinsTAATG
NM_014384.3:c.1195+265_1195+269delinsTAATG MANE Select	NP_055199.1:n.1195+265_1195+269delinsTAATG