Canonical Allele Identifier: CA2010874576

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262580C= , CM000673.2:g.134262580C=	GRCh38
NC_000011.9:g.134132474C= , CM000673.1:g.134132474C=	GRCh37
NC_000011.8:g.133637684C=	NCBI36
NG_015842.1:g.14041C= , LRG_448:g.14041C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1153C= MANE Select	ENSP00000281182.5:p.Gln385=
ENST00000281182.8:c.1153C=	ENSP00000281182.4:p.Gln385=
ENST00000374752.6:c.772C=	ENSP00000363884.4:p.Gln258=
ENST00000524426.5:c.*883C=	ENSP00000431310.1:n.*883C=
ENST00000524502.2:n.153C=
ENST00000526026.5:c.*842C=	ENSP00000431532.1:n.*842C=
ENST00000531338.5:n.1397C=
ENST00000533387.5:n.2212C=
NM_014384.2:c.1153C= , LRG_448t1:c.1153C=	NP_055199.1:p.Gln385=
XM_005271501.2:c.1153C=	XP_005271558.1:p.Gln385=
XM_011542750.1:c.1153C=	XP_011541052.1:p.Gln385=
XR_947819.1:n.1217C=
XR_947820.1:n.1605C=
XR_947821.1:n.1362C=
XR_947822.1:n.1047C=
XR_947823.1:n.1203C=
XM_005271505.4:c.*1418C=	XP_005271562.1:n.*1418C=
XM_011542750.3:c.1153C=	XP_011541052.1:p.Gln385=
XM_017017542.2:c.1153C=	XP_016873031.1:p.Gln385=
XM_017017543.2:c.1153C=	XP_016873032.1:p.Gln385=
XM_017017544.2:c.*122C=	XP_016873033.1:n.*122C=
XM_017017545.2:c.*365C=	XP_016873034.1:n.*365C=
XM_017017546.2:c.859C=	XP_016873035.1:p.Gln287=
XM_017017547.2:c.859C=	XP_016873036.1:p.Gln287=
XM_017017548.2:c.*1789C=	XP_016873037.1:n.*1789C=
XM_017017549.2:c.*1563C=	XP_016873038.1:n.*1563C=
XM_024448437.1:c.*300C=	XP_024304205.1:n.*300C=
XM_024448438.1:c.772C=	XP_024304206.1:p.Gln258=
NM_014384.3:c.1153C= MANE Select	NP_055199.1:p.Gln385=