Canonical Allele Identifier: CA2010874584

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262583C= , CM000673.2:g.134262583C=	GRCh38
NC_000011.9:g.134132477C= , CM000673.1:g.134132477C=	GRCh37
NC_000011.8:g.133637687C=	NCBI36
NG_015842.1:g.14044C= , LRG_448:g.14044C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1156C= MANE Select	ENSP00000281182.5:p.Gln386=
ENST00000281182.8:c.1156C=	ENSP00000281182.4:p.Gln386=
ENST00000374752.6:c.775C=	ENSP00000363884.4:p.Gln259=
ENST00000524426.5:c.*886C=	ENSP00000431310.1:n.*886C=
ENST00000524502.2:n.156C=
ENST00000526026.5:c.*845C=	ENSP00000431532.1:n.*845C=
ENST00000531338.5:n.1400C=
ENST00000533387.5:n.2215C=
NM_014384.2:c.1156C= , LRG_448t1:c.1156C=	NP_055199.1:p.Gln386=
XM_005271501.2:c.1156C=	XP_005271558.1:p.Gln386=
XM_011542750.1:c.1156C=	XP_011541052.1:p.Gln386=
XR_947819.1:n.1220C=
XR_947820.1:n.1608C=
XR_947821.1:n.1365C=
XR_947822.1:n.1050C=
XR_947823.1:n.1206C=
XM_005271505.4:c.*1421C=	XP_005271562.1:n.*1421C=
XM_011542750.3:c.1156C=	XP_011541052.1:p.Gln386=
XM_017017542.2:c.1156C=	XP_016873031.1:p.Gln386=
XM_017017543.2:c.1156C=	XP_016873032.1:p.Gln386=
XM_017017544.2:c.*125C=	XP_016873033.1:n.*125C=
XM_017017545.2:c.*368C=	XP_016873034.1:n.*368C=
XM_017017546.2:c.862C=	XP_016873035.1:p.Gln288=
XM_017017547.2:c.862C=	XP_016873036.1:p.Gln288=
XM_017017548.2:c.*1792C=	XP_016873037.1:n.*1792C=
XM_017017549.2:c.*1566C=	XP_016873038.1:n.*1566C=
XM_024448437.1:c.*303C=	XP_024304205.1:n.*303C=
XM_024448438.1:c.775C=	XP_024304206.1:p.Gln259=
NM_014384.3:c.1156C= MANE Select	NP_055199.1:p.Gln386=