Canonical Allele Identifier: CA2010874430

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262471T= , CM000673.2:g.134262471T=	GRCh38
NC_000011.9:g.134132365T= , CM000673.1:g.134132365T=	GRCh37
NC_000011.8:g.133637575T=	NCBI36
NG_015842.1:g.13932T= , LRG_448:g.13932T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1093-49T= MANE Select	ENSP00000281182.5:n.1093-49T=
ENST00000281182.8:c.1093-49T=	ENSP00000281182.4:n.1093-49T=
ENST00000374752.6:c.712-49T=	ENSP00000363884.4:n.712-49T=
ENST00000524426.5:c.*823-49T=	ENSP00000431310.1:n.*823-49T=
ENST00000524502.2:n.93-49T=
ENST00000524547.5:n.696-49T=
ENST00000526026.5:c.*782-49T=	ENSP00000431532.1:n.*782-49T=
ENST00000531338.5:n.1288T=
ENST00000533387.5:n.2152-49T=
NM_014384.2:c.1093-49T= , LRG_448t1:c.1093-49T=	NP_055199.1:n.1093-49T=
XM_005271501.2:c.1093-49T=	XP_005271558.1:n.1093-49T=
XM_011542750.1:c.1093-49T=	XP_011541052.1:n.1093-49T=
XR_947819.1:n.1157-49T=
XR_947820.1:n.1496T=
XR_947821.1:n.1302-49T=
XR_947822.1:n.987-49T=
XR_947823.1:n.1143-49T=
XM_005271505.4:c.*1358-49T=	XP_005271562.1:n.*1358-49T=
XM_011542750.3:c.1093-49T=	XP_011541052.1:n.1093-49T=
XM_017017542.2:c.1093-49T=	XP_016873031.1:n.1093-49T=
XM_017017543.2:c.1093-49T=	XP_016873032.1:n.1093-49T=
XM_017017544.2:c.*62-49T=	XP_016873033.1:n.*62-49T=
XM_017017545.2:c.*256T=	XP_016873034.1:n.*256T=
XM_017017546.2:c.799-49T=	XP_016873035.1:n.799-49T=
XM_017017547.2:c.799-49T=	XP_016873036.1:n.799-49T=
XM_017017548.2:c.*1729-49T=	XP_016873037.1:n.*1729-49T=
XM_017017549.2:c.*1503-49T=	XP_016873038.1:n.*1503-49T=
XM_024448437.1:c.*191T=	XP_024304205.1:n.*191T=
XM_024448438.1:c.712-49T=	XP_024304206.1:n.712-49T=
NM_014384.3:c.1093-49T= MANE Select	NP_055199.1:n.1093-49T=