Canonical Allele Identifier: CA2010874604

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262594G= , CM000673.2:g.134262594G=	GRCh38
NC_000011.9:g.134132488G= , CM000673.1:g.134132488G=	GRCh37
NC_000011.8:g.133637698G=	NCBI36
NG_015842.1:g.14055G= , LRG_448:g.14055G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1167G= MANE Select	ENSP00000281182.5:p.Arg389=
ENST00000281182.8:c.1167G=	ENSP00000281182.4:p.Arg389=
ENST00000374752.6:c.786G=	ENSP00000363884.4:p.Arg262=
ENST00000524426.5:c.*897G=	ENSP00000431310.1:n.*897G=
ENST00000524502.2:n.167G=
ENST00000526026.5:c.*856G=	ENSP00000431532.1:n.*856G=
ENST00000531338.5:n.1411G=
ENST00000533387.5:n.2226G=
NM_014384.2:c.1167G= , LRG_448t1:c.1167G=	NP_055199.1:p.Arg389=
XM_005271501.2:c.1167G=	XP_005271558.1:p.Arg389=
XM_011542750.1:c.1167G=	XP_011541052.1:p.Arg389=
XR_947819.1:n.1231G=
XR_947820.1:n.1619G=
XR_947821.1:n.1376G=
XR_947822.1:n.1061G=
XR_947823.1:n.1217G=
XM_005271505.4:c.*1432G=	XP_005271562.1:n.*1432G=
XM_011542750.3:c.1167G=	XP_011541052.1:p.Arg389=
XM_017017542.2:c.1167G=	XP_016873031.1:p.Arg389=
XM_017017543.2:c.1167G=	XP_016873032.1:p.Arg389=
XM_017017544.2:c.*136G=	XP_016873033.1:n.*136G=
XM_017017545.2:c.*379G=	XP_016873034.1:n.*379G=
XM_017017546.2:c.873G=	XP_016873035.1:p.Arg291=
XM_017017547.2:c.873G=	XP_016873036.1:p.Arg291=
XM_017017548.2:c.*1803G=	XP_016873037.1:n.*1803G=
XM_017017549.2:c.*1577G=	XP_016873038.1:n.*1577G=
XM_024448437.1:c.*314G=	XP_024304205.1:n.*314G=
XM_024448438.1:c.786G=	XP_024304206.1:p.Arg262=
NM_014384.3:c.1167G= MANE Select	NP_055199.1:p.Arg389=