Canonical Allele Identifier: CA2010874593

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262588C= , CM000673.2:g.134262588C=	GRCh38
NC_000011.9:g.134132482C= , CM000673.1:g.134132482C=	GRCh37
NC_000011.8:g.133637692C=	NCBI36
NG_015842.1:g.14049C= , LRG_448:g.14049C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1161C= MANE Select	ENSP00000281182.5:p.Tyr387=
ENST00000281182.8:c.1161C=	ENSP00000281182.4:p.Tyr387=
ENST00000374752.6:c.780C=	ENSP00000363884.4:p.Tyr260=
ENST00000524426.5:c.*891C=	ENSP00000431310.1:n.*891C=
ENST00000524502.2:n.161C=
ENST00000526026.5:c.*850C=	ENSP00000431532.1:n.*850C=
ENST00000531338.5:n.1405C=
ENST00000533387.5:n.2220C=
NM_014384.2:c.1161C= , LRG_448t1:c.1161C=	NP_055199.1:p.Tyr387=
XM_005271501.2:c.1161C=	XP_005271558.1:p.Tyr387=
XM_011542750.1:c.1161C=	XP_011541052.1:p.Tyr387=
XR_947819.1:n.1225C=
XR_947820.1:n.1613C=
XR_947821.1:n.1370C=
XR_947822.1:n.1055C=
XR_947823.1:n.1211C=
XM_005271505.4:c.*1426C=	XP_005271562.1:n.*1426C=
XM_011542750.3:c.1161C=	XP_011541052.1:p.Tyr387=
XM_017017542.2:c.1161C=	XP_016873031.1:p.Tyr387=
XM_017017543.2:c.1161C=	XP_016873032.1:p.Tyr387=
XM_017017544.2:c.*130C=	XP_016873033.1:n.*130C=
XM_017017545.2:c.*373C=	XP_016873034.1:n.*373C=
XM_017017546.2:c.867C=	XP_016873035.1:p.Tyr289=
XM_017017547.2:c.867C=	XP_016873036.1:p.Tyr289=
XM_017017548.2:c.*1797C=	XP_016873037.1:n.*1797C=
XM_017017549.2:c.*1571C=	XP_016873038.1:n.*1571C=
XM_024448437.1:c.*308C=	XP_024304205.1:n.*308C=
XM_024448438.1:c.780C=	XP_024304206.1:p.Tyr260=
NM_014384.3:c.1161C= MANE Select	NP_055199.1:p.Tyr387=