Canonical Allele Identifier: CA2010874619

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262607C= , CM000673.2:g.134262607C=	GRCh38
NC_000011.9:g.134132501C= , CM000673.1:g.134132501C=	GRCh37
NC_000011.8:g.133637711C=	NCBI36
NG_015842.1:g.14068C= , LRG_448:g.14068C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1180C= MANE Select	ENSP00000281182.5:p.His394=
ENST00000281182.8:c.1180C=	ENSP00000281182.4:p.His394=
ENST00000374752.6:c.799C=	ENSP00000363884.4:p.His267=
ENST00000524426.5:c.*910C=	ENSP00000431310.1:n.*910C=
ENST00000524502.2:n.180C=
ENST00000526026.5:c.*869C=	ENSP00000431532.1:n.*869C=
ENST00000531338.5:n.1424C=
ENST00000533387.5:n.2239C=
NM_014384.2:c.1180C= , LRG_448t1:c.1180C=	NP_055199.1:p.His394=
XM_005271501.2:c.1180C=	XP_005271558.1:p.His394=
XM_011542750.1:c.1180C=	XP_011541052.1:p.His394=
XR_947819.1:n.1244C=
XR_947820.1:n.1632C=
XR_947822.1:n.1074C=
XR_947823.1:n.1230C=
XM_005271505.4:c.*1445C=	XP_005271562.1:n.*1445C=
XM_011542750.3:c.1180C=	XP_011541052.1:p.His394=
XM_017017542.2:c.1180C=	XP_016873031.1:p.His394=
XM_017017543.2:c.1180C=	XP_016873032.1:p.His394=
XM_017017544.2:c.*149C=	XP_016873033.1:n.*149C=
XM_017017545.2:c.*392C=	XP_016873034.1:n.*392C=
XM_017017546.2:c.886C=	XP_016873035.1:p.His296=
XM_017017547.2:c.886C=	XP_016873036.1:p.His296=
XM_017017548.2:c.*1816C=	XP_016873037.1:n.*1816C=
XM_017017549.2:c.*1590C=	XP_016873038.1:n.*1590C=
XM_024448437.1:c.*327C=	XP_024304205.1:n.*327C=
XM_024448438.1:c.799C=	XP_024304206.1:p.His267=
NM_014384.3:c.1180C= MANE Select	NP_055199.1:p.His394=