Canonical Allele Identifier: CA2010874605

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262595G= , CM000673.2:g.134262595G=	GRCh38
NC_000011.9:g.134132489G= , CM000673.1:g.134132489G=	GRCh37
NC_000011.8:g.133637699G=	NCBI36
NG_015842.1:g.14056G= , LRG_448:g.14056G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1168G= MANE Select	ENSP00000281182.5:p.Asp390=
ENST00000281182.8:c.1168G=	ENSP00000281182.4:p.Asp390=
ENST00000374752.6:c.787G=	ENSP00000363884.4:p.Asp263=
ENST00000524426.5:c.*898G=	ENSP00000431310.1:n.*898G=
ENST00000524502.2:n.168G=
ENST00000526026.5:c.*857G=	ENSP00000431532.1:n.*857G=
ENST00000531338.5:n.1412G=
ENST00000533387.5:n.2227G=
NM_014384.2:c.1168G= , LRG_448t1:c.1168G=	NP_055199.1:p.Asp390=
XM_005271501.2:c.1168G=	XP_005271558.1:p.Asp390=
XM_011542750.1:c.1168G=	XP_011541052.1:p.Asp390=
XR_947819.1:n.1232G=
XR_947820.1:n.1620G=
XR_947821.1:n.1377G=
XR_947822.1:n.1062G=
XR_947823.1:n.1218G=
XM_005271505.4:c.*1433G=	XP_005271562.1:n.*1433G=
XM_011542750.3:c.1168G=	XP_011541052.1:p.Asp390=
XM_017017542.2:c.1168G=	XP_016873031.1:p.Asp390=
XM_017017543.2:c.1168G=	XP_016873032.1:p.Asp390=
XM_017017544.2:c.*137G=	XP_016873033.1:n.*137G=
XM_017017545.2:c.*380G=	XP_016873034.1:n.*380G=
XM_017017546.2:c.874G=	XP_016873035.1:p.Asp292=
XM_017017547.2:c.874G=	XP_016873036.1:p.Asp292=
XM_017017548.2:c.*1804G=	XP_016873037.1:n.*1804G=
XM_017017549.2:c.*1578G=	XP_016873038.1:n.*1578G=
XM_024448437.1:c.*315G=	XP_024304205.1:n.*315G=
XM_024448438.1:c.787G=	XP_024304206.1:p.Asp263=
NM_014384.3:c.1168G= MANE Select	NP_055199.1:p.Asp390=