Canonical Allele Identifier: CA2010874526

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262557G= , CM000673.2:g.134262557G=	GRCh38
NC_000011.9:g.134132451G= , CM000673.1:g.134132451G=	GRCh37
NC_000011.8:g.133637661G=	NCBI36
NG_015842.1:g.14018G= , LRG_448:g.14018G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1130G= MANE Select	ENSP00000281182.5:p.Gly377=
ENST00000281182.8:c.1130G=	ENSP00000281182.4:p.Gly377=
ENST00000374752.6:c.749G=	ENSP00000363884.4:p.Gly250=
ENST00000524426.5:c.*860G=	ENSP00000431310.1:n.*860G=
ENST00000524502.2:n.130G=
ENST00000526026.5:c.*819G=	ENSP00000431532.1:n.*819G=
ENST00000531338.5:n.1374G=
ENST00000533387.5:n.2189G=
NM_014384.2:c.1130G= , LRG_448t1:c.1130G=	NP_055199.1:p.Gly377=
XM_005271501.2:c.1130G=	XP_005271558.1:p.Gly377=
XM_011542750.1:c.1130G=	XP_011541052.1:p.Gly377=
XR_947819.1:n.1194G=
XR_947820.1:n.1582G=
XR_947821.1:n.1339G=
XR_947822.1:n.1024G=
XR_947823.1:n.1180G=
XM_005271505.4:c.*1395G=	XP_005271562.1:n.*1395G=
XM_011542750.3:c.1130G=	XP_011541052.1:p.Gly377=
XM_017017542.2:c.1130G=	XP_016873031.1:p.Gly377=
XM_017017543.2:c.1130G=	XP_016873032.1:p.Gly377=
XM_017017544.2:c.*99G=	XP_016873033.1:n.*99G=
XM_017017545.2:c.*342G=	XP_016873034.1:n.*342G=
XM_017017546.2:c.836G=	XP_016873035.1:p.Gly279=
XM_017017547.2:c.836G=	XP_016873036.1:p.Gly279=
XM_017017548.2:c.*1766G=	XP_016873037.1:n.*1766G=
XM_017017549.2:c.*1540G=	XP_016873038.1:n.*1540G=
XM_024448437.1:c.*277G=	XP_024304205.1:n.*277G=
XM_024448438.1:c.749G=	XP_024304206.1:p.Gly250=
NM_014384.3:c.1130G= MANE Select	NP_055199.1:p.Gly377=