Canonical Allele Identifier: CA2010874503

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262547G= , CM000673.2:g.134262547G=	GRCh38
NC_000011.9:g.134132441G= , CM000673.1:g.134132441G=	GRCh37
NC_000011.8:g.133637651G=	NCBI36
NG_015842.1:g.14008G= , LRG_448:g.14008G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1120G= MANE Select	ENSP00000281182.5:p.Gly374=
ENST00000281182.8:c.1120G=	ENSP00000281182.4:p.Gly374=
ENST00000374752.6:c.739G=	ENSP00000363884.4:p.Gly247=
ENST00000524426.5:c.*850G=	ENSP00000431310.1:n.*850G=
ENST00000524502.2:n.120G=
ENST00000526026.5:c.*809G=	ENSP00000431532.1:n.*809G=
ENST00000531338.5:n.1364G=
ENST00000533387.5:n.2179G=
NM_014384.2:c.1120G= , LRG_448t1:c.1120G=	NP_055199.1:p.Gly374=
XM_005271501.2:c.1120G=	XP_005271558.1:p.Gly374=
XM_011542750.1:c.1120G=	XP_011541052.1:p.Gly374=
XR_947819.1:n.1184G=
XR_947820.1:n.1572G=
XR_947821.1:n.1329G=
XR_947822.1:n.1014G=
XR_947823.1:n.1170G=
XM_005271505.4:c.*1385G=	XP_005271562.1:n.*1385G=
XM_011542750.3:c.1120G=	XP_011541052.1:p.Gly374=
XM_017017542.2:c.1120G=	XP_016873031.1:p.Gly374=
XM_017017543.2:c.1120G=	XP_016873032.1:p.Gly374=
XM_017017544.2:c.*89G=	XP_016873033.1:n.*89G=
XM_017017545.2:c.*332G=	XP_016873034.1:n.*332G=
XM_017017546.2:c.826G=	XP_016873035.1:p.Gly276=
XM_017017547.2:c.826G=	XP_016873036.1:p.Gly276=
XM_017017548.2:c.*1756G=	XP_016873037.1:n.*1756G=
XM_017017549.2:c.*1530G=	XP_016873038.1:n.*1530G=
XM_024448437.1:c.*267G=	XP_024304205.1:n.*267G=
XM_024448438.1:c.739G=	XP_024304206.1:p.Gly247=
NM_014384.3:c.1120G= MANE Select	NP_055199.1:p.Gly374=