Canonical Allele Identifier: CA2010874555

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262568G= , CM000673.2:g.134262568G=	GRCh38
NC_000011.9:g.134132462G= , CM000673.1:g.134132462G=	GRCh37
NC_000011.8:g.133637672G=	NCBI36
NG_015842.1:g.14029G= , LRG_448:g.14029G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1141G= MANE Select	ENSP00000281182.5:p.Asp381=
ENST00000281182.8:c.1141G=	ENSP00000281182.4:p.Asp381=
ENST00000374752.6:c.760G=	ENSP00000363884.4:p.Asp254=
ENST00000524426.5:c.*871G=	ENSP00000431310.1:n.*871G=
ENST00000524502.2:n.141G=
ENST00000526026.5:c.*830G=	ENSP00000431532.1:n.*830G=
ENST00000531338.5:n.1385G=
ENST00000533387.5:n.2200G=
NM_014384.2:c.1141G= , LRG_448t1:c.1141G=	NP_055199.1:p.Asp381=
XM_005271501.2:c.1141G=	XP_005271558.1:p.Asp381=
XM_011542750.1:c.1141G=	XP_011541052.1:p.Asp381=
XR_947819.1:n.1205G=
XR_947820.1:n.1593G=
XR_947821.1:n.1350G=
XR_947822.1:n.1035G=
XR_947823.1:n.1191G=
XM_005271505.4:c.*1406G=	XP_005271562.1:n.*1406G=
XM_011542750.3:c.1141G=	XP_011541052.1:p.Asp381=
XM_017017542.2:c.1141G=	XP_016873031.1:p.Asp381=
XM_017017543.2:c.1141G=	XP_016873032.1:p.Asp381=
XM_017017544.2:c.*110G=	XP_016873033.1:n.*110G=
XM_017017545.2:c.*353G=	XP_016873034.1:n.*353G=
XM_017017546.2:c.847G=	XP_016873035.1:p.Asp283=
XM_017017547.2:c.847G=	XP_016873036.1:p.Asp283=
XM_017017548.2:c.*1777G=	XP_016873037.1:n.*1777G=
XM_017017549.2:c.*1551G=	XP_016873038.1:n.*1551G=
XM_024448437.1:c.*288G=	XP_024304205.1:n.*288G=
XM_024448438.1:c.760G=	XP_024304206.1:p.Asp254=
NM_014384.3:c.1141G= MANE Select	NP_055199.1:p.Asp381=