Canonical Allele Identifier: CA2010874479

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262524G= , CM000673.2:g.134262524G=	GRCh38
NC_000011.9:g.134132418G= , CM000673.1:g.134132418G=	GRCh37
NC_000011.8:g.133637628G=	NCBI36
NG_015842.1:g.13985G= , LRG_448:g.13985G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1097G= MANE Select	ENSP00000281182.5:p.Cys366=
ENST00000281182.8:c.1097G=	ENSP00000281182.4:p.Cys366=
ENST00000374752.6:c.716G=	ENSP00000363884.4:p.Cys239=
ENST00000524426.5:c.*827G=	ENSP00000431310.1:n.*827G=
ENST00000524502.2:n.97G=
ENST00000524547.5:n.700G=
ENST00000526026.5:c.*786G=	ENSP00000431532.1:n.*786G=
ENST00000531338.5:n.1341G=
ENST00000533387.5:n.2156G=
NM_014384.2:c.1097G= , LRG_448t1:c.1097G=	NP_055199.1:p.Cys366=
XM_005271501.2:c.1097G=	XP_005271558.1:p.Cys366=
XM_011542750.1:c.1097G=	XP_011541052.1:p.Cys366=
XR_947819.1:n.1161G=
XR_947820.1:n.1549G=
XR_947821.1:n.1306G=
XR_947822.1:n.991G=
XR_947823.1:n.1147G=
XM_005271505.4:c.*1362G=	XP_005271562.1:n.*1362G=
XM_011542750.3:c.1097G=	XP_011541052.1:p.Cys366=
XM_017017542.2:c.1097G=	XP_016873031.1:p.Cys366=
XM_017017543.2:c.1097G=	XP_016873032.1:p.Cys366=
XM_017017544.2:c.*66G=	XP_016873033.1:n.*66G=
XM_017017545.2:c.*309G=	XP_016873034.1:n.*309G=
XM_017017546.2:c.803G=	XP_016873035.1:p.Cys268=
XM_017017547.2:c.803G=	XP_016873036.1:p.Cys268=
XM_017017548.2:c.*1733G=	XP_016873037.1:n.*1733G=
XM_017017549.2:c.*1507G=	XP_016873038.1:n.*1507G=
XM_024448437.1:c.*244G=	XP_024304205.1:n.*244G=
XM_024448438.1:c.716G=	XP_024304206.1:p.Cys239=
NM_014384.3:c.1097G= MANE Select	NP_055199.1:p.Cys366=