Canonical Allele Identifier: CA2010874622

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262609C= , CM000673.2:g.134262609C=	GRCh38
NC_000011.9:g.134132503C= , CM000673.1:g.134132503C=	GRCh37
NC_000011.8:g.133637713C=	NCBI36
NG_015842.1:g.14070C= , LRG_448:g.14070C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1182C= MANE Select	ENSP00000281182.5:p.His394=
ENST00000281182.8:c.1182C=	ENSP00000281182.4:p.His394=
ENST00000374752.6:c.801C=	ENSP00000363884.4:p.His267=
ENST00000524426.5:c.*912C=	ENSP00000431310.1:n.*912C=
ENST00000524502.2:n.182C=
ENST00000526026.5:c.*871C=	ENSP00000431532.1:n.*871C=
ENST00000531338.5:n.1426C=
ENST00000533387.5:n.2241C=
NM_014384.2:c.1182C= , LRG_448t1:c.1182C=	NP_055199.1:p.His394=
XM_005271501.2:c.1182C=	XP_005271558.1:p.His394=
XM_011542750.1:c.1182C=	XP_011541052.1:p.His394=
XR_947819.1:n.1246C=
XR_947820.1:n.1634C=
XR_947822.1:n.1076C=
XR_947823.1:n.1232C=
XM_005271505.4:c.*1447C=	XP_005271562.1:n.*1447C=
XM_011542750.3:c.1182C=	XP_011541052.1:p.His394=
XM_017017542.2:c.1182C=	XP_016873031.1:p.His394=
XM_017017543.2:c.1182C=	XP_016873032.1:p.His394=
XM_017017544.2:c.*151C=	XP_016873033.1:n.*151C=
XM_017017545.2:c.*394C=	XP_016873034.1:n.*394C=
XM_017017546.2:c.888C=	XP_016873035.1:p.His296=
XM_017017547.2:c.888C=	XP_016873036.1:p.His296=
XM_017017548.2:c.*1818C=	XP_016873037.1:n.*1818C=
XM_017017549.2:c.*1592C=	XP_016873038.1:n.*1592C=
XM_024448437.1:c.*329C=	XP_024304205.1:n.*329C=
XM_024448438.1:c.801C=	XP_024304206.1:p.His267=
NM_014384.3:c.1182C= MANE Select	NP_055199.1:p.His394=