Canonical Allele Identifier: CA2010874564

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262573C= , CM000673.2:g.134262573C=	GRCh38
NC_000011.9:g.134132467C= , CM000673.1:g.134132467C=	GRCh37
NC_000011.8:g.133637677C=	NCBI36
NG_015842.1:g.14034C= , LRG_448:g.14034C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1146C= MANE Select	ENSP00000281182.5:p.Tyr382=
ENST00000281182.8:c.1146C=	ENSP00000281182.4:p.Tyr382=
ENST00000374752.6:c.765C=	ENSP00000363884.4:p.Tyr255=
ENST00000524426.5:c.*876C=	ENSP00000431310.1:n.*876C=
ENST00000524502.2:n.146C=
ENST00000526026.5:c.*835C=	ENSP00000431532.1:n.*835C=
ENST00000531338.5:n.1390C=
ENST00000533387.5:n.2205C=
NM_014384.2:c.1146C= , LRG_448t1:c.1146C=	NP_055199.1:p.Tyr382=
XM_005271501.2:c.1146C=	XP_005271558.1:p.Tyr382=
XM_011542750.1:c.1146C=	XP_011541052.1:p.Tyr382=
XR_947819.1:n.1210C=
XR_947820.1:n.1598C=
XR_947821.1:n.1355C=
XR_947822.1:n.1040C=
XR_947823.1:n.1196C=
XM_005271505.4:c.*1411C=	XP_005271562.1:n.*1411C=
XM_011542750.3:c.1146C=	XP_011541052.1:p.Tyr382=
XM_017017542.2:c.1146C=	XP_016873031.1:p.Tyr382=
XM_017017543.2:c.1146C=	XP_016873032.1:p.Tyr382=
XM_017017544.2:c.*115C=	XP_016873033.1:n.*115C=
XM_017017545.2:c.*358C=	XP_016873034.1:n.*358C=
XM_017017546.2:c.852C=	XP_016873035.1:p.Tyr284=
XM_017017547.2:c.852C=	XP_016873036.1:p.Tyr284=
XM_017017548.2:c.*1782C=	XP_016873037.1:n.*1782C=
XM_017017549.2:c.*1556C=	XP_016873038.1:n.*1556C=
XM_024448437.1:c.*293C=	XP_024304205.1:n.*293C=
XM_024448438.1:c.765C=	XP_024304206.1:p.Tyr255=
NM_014384.3:c.1146C= MANE Select	NP_055199.1:p.Tyr382=