Canonical Allele Identifier: CA2010874579

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262581A= , CM000673.2:g.134262581A=	GRCh38
NC_000011.9:g.134132475A= , CM000673.1:g.134132475A=	GRCh37
NC_000011.8:g.133637685A=	NCBI36
NG_015842.1:g.14042A= , LRG_448:g.14042A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1154A= MANE Select	ENSP00000281182.5:p.Gln385=
ENST00000281182.8:c.1154A=	ENSP00000281182.4:p.Gln385=
ENST00000374752.6:c.773A=	ENSP00000363884.4:p.Gln258=
ENST00000524426.5:c.*884A=	ENSP00000431310.1:n.*884A=
ENST00000524502.2:n.154A=
ENST00000526026.5:c.*843A=	ENSP00000431532.1:n.*843A=
ENST00000531338.5:n.1398A=
ENST00000533387.5:n.2213A=
NM_014384.2:c.1154A= , LRG_448t1:c.1154A=	NP_055199.1:p.Gln385=
XM_005271501.2:c.1154A=	XP_005271558.1:p.Gln385=
XM_011542750.1:c.1154A=	XP_011541052.1:p.Gln385=
XR_947819.1:n.1218A=
XR_947820.1:n.1606A=
XR_947821.1:n.1363A=
XR_947822.1:n.1048A=
XR_947823.1:n.1204A=
XM_005271505.4:c.*1419A=	XP_005271562.1:n.*1419A=
XM_011542750.3:c.1154A=	XP_011541052.1:p.Gln385=
XM_017017542.2:c.1154A=	XP_016873031.1:p.Gln385=
XM_017017543.2:c.1154A=	XP_016873032.1:p.Gln385=
XM_017017544.2:c.*123A=	XP_016873033.1:n.*123A=
XM_017017545.2:c.*366A=	XP_016873034.1:n.*366A=
XM_017017546.2:c.860A=	XP_016873035.1:p.Gln287=
XM_017017547.2:c.860A=	XP_016873036.1:p.Gln287=
XM_017017548.2:c.*1790A=	XP_016873037.1:n.*1790A=
XM_017017549.2:c.*1564A=	XP_016873038.1:n.*1564A=
XM_024448437.1:c.*301A=	XP_024304205.1:n.*301A=
XM_024448438.1:c.773A=	XP_024304206.1:p.Gln258=
NM_014384.3:c.1154A= MANE Select	NP_055199.1:p.Gln385=