Canonical Allele Identifier: CA2739353413

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262851T>A , CM000673.2:g.134262851T>A	GRCh38
NC_000011.9:g.134132745T>A , CM000673.1:g.134132745T>A	GRCh37
NC_000011.8:g.133637955T>A	NCBI36
NG_015842.1:g.14312T>A , LRG_448:g.14312T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1195+229T>A MANE Select	ENSP00000281182.5:n.1195+229T>A
ENST00000281182.8:c.1195+229T>A	ENSP00000281182.4:n.1195+229T>A
ENST00000374752.6:c.814+229T>A	ENSP00000363884.4:n.814+229T>A
ENST00000524502.2:n.277T>A
ENST00000526026.5:c.*966T>A	ENSP00000431532.1:n.*966T>A
ENST00000531338.5:n.1668T>A
ENST00000533387.5:n.2254+229T>A
NM_014384.2:c.1195+229T>A , LRG_448t1:c.1195+229T>A	NP_055199.1:n.1195+229T>A
XM_005271501.2:c.1277T>A	XP_005271558.1:p.Phe426Tyr
XM_011542750.1:c.1195+229T>A	XP_011541052.1:n.1195+229T>A
XR_947819.1:n.1259+229T>A
XR_947820.1:n.1876T>A
XR_947822.1:n.1089+229T>A
XR_947823.1:n.1245+229T>A
XM_005271505.4:c.*1460+229T>A	XP_005271562.1:n.*1460+229T>A
XM_011542750.3:c.1195+229T>A	XP_011541052.1:n.1195+229T>A
XM_017017542.2:c.1195+229T>A	XP_016873031.1:n.1195+229T>A
XM_017017543.2:c.1277T>A	XP_016873032.1:p.Phe426Tyr
XM_017017544.2:c.*164+229T>A	XP_016873033.1:n.*164+229T>A
XM_017017545.2:c.*636T>A	XP_016873034.1:n.*636T>A
XM_017017546.2:c.901+229T>A	XP_016873035.1:n.901+229T>A
XM_017017547.2:c.901+229T>A	XP_016873036.1:n.901+229T>A
XM_017017548.2:c.*1913T>A	XP_016873037.1:n.*1913T>A
XM_017017549.2:c.*1605+229T>A	XP_016873038.1:n.*1605+229T>A
XM_024448437.1:c.*571T>A	XP_024304205.1:n.*571T>A
XM_024448438.1:c.814+229T>A	XP_024304206.1:n.814+229T>A
NM_014384.3:c.1195+229T>A MANE Select	NP_055199.1:n.1195+229T>A