Canonical Allele Identifier: CA2010874510

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262551G= , CM000673.2:g.134262551G=	GRCh38
NC_000011.9:g.134132445G= , CM000673.1:g.134132445G=	GRCh37
NC_000011.8:g.133637655G=	NCBI36
NG_015842.1:g.14012G= , LRG_448:g.14012G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1124G= MANE Select	ENSP00000281182.5:p.Gly375=
ENST00000281182.8:c.1124G=	ENSP00000281182.4:p.Gly375=
ENST00000374752.6:c.743G=	ENSP00000363884.4:p.Gly248=
ENST00000524426.5:c.*854G=	ENSP00000431310.1:n.*854G=
ENST00000524502.2:n.124G=
ENST00000526026.5:c.*813G=	ENSP00000431532.1:n.*813G=
ENST00000531338.5:n.1368G=
ENST00000533387.5:n.2183G=
NM_014384.2:c.1124G= , LRG_448t1:c.1124G=	NP_055199.1:p.Gly375=
XM_005271501.2:c.1124G=	XP_005271558.1:p.Gly375=
XM_011542750.1:c.1124G=	XP_011541052.1:p.Gly375=
XR_947819.1:n.1188G=
XR_947820.1:n.1576G=
XR_947821.1:n.1333G=
XR_947822.1:n.1018G=
XR_947823.1:n.1174G=
XM_005271505.4:c.*1389G=	XP_005271562.1:n.*1389G=
XM_011542750.3:c.1124G=	XP_011541052.1:p.Gly375=
XM_017017542.2:c.1124G=	XP_016873031.1:p.Gly375=
XM_017017543.2:c.1124G=	XP_016873032.1:p.Gly375=
XM_017017544.2:c.*93G=	XP_016873033.1:n.*93G=
XM_017017545.2:c.*336G=	XP_016873034.1:n.*336G=
XM_017017546.2:c.830G=	XP_016873035.1:p.Gly277=
XM_017017547.2:c.830G=	XP_016873036.1:p.Gly277=
XM_017017548.2:c.*1760G=	XP_016873037.1:n.*1760G=
XM_017017549.2:c.*1534G=	XP_016873038.1:n.*1534G=
XM_024448437.1:c.*271G=	XP_024304205.1:n.*271G=
XM_024448438.1:c.743G=	XP_024304206.1:p.Gly248=
NM_014384.3:c.1124G= MANE Select	NP_055199.1:p.Gly375=