Canonical Allele Identifier: CA2010874500

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262546C= , CM000673.2:g.134262546C=	GRCh38
NC_000011.9:g.134132440C= , CM000673.1:g.134132440C=	GRCh37
NC_000011.8:g.133637650C=	NCBI36
NG_015842.1:g.14007C= , LRG_448:g.14007C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1119C= MANE Select	ENSP00000281182.5:p.His373=
ENST00000281182.8:c.1119C=	ENSP00000281182.4:p.His373=
ENST00000374752.6:c.738C=	ENSP00000363884.4:p.His246=
ENST00000524426.5:c.*849C=	ENSP00000431310.1:n.*849C=
ENST00000524502.2:n.119C=
ENST00000526026.5:c.*808C=	ENSP00000431532.1:n.*808C=
ENST00000531338.5:n.1363C=
ENST00000533387.5:n.2178C=
NM_014384.2:c.1119C= , LRG_448t1:c.1119C=	NP_055199.1:p.His373=
XM_005271501.2:c.1119C=	XP_005271558.1:p.His373=
XM_011542750.1:c.1119C=	XP_011541052.1:p.His373=
XR_947819.1:n.1183C=
XR_947820.1:n.1571C=
XR_947821.1:n.1328C=
XR_947822.1:n.1013C=
XR_947823.1:n.1169C=
XM_005271505.4:c.*1384C=	XP_005271562.1:n.*1384C=
XM_011542750.3:c.1119C=	XP_011541052.1:p.His373=
XM_017017542.2:c.1119C=	XP_016873031.1:p.His373=
XM_017017543.2:c.1119C=	XP_016873032.1:p.His373=
XM_017017544.2:c.*88C=	XP_016873033.1:n.*88C=
XM_017017545.2:c.*331C=	XP_016873034.1:n.*331C=
XM_017017546.2:c.825C=	XP_016873035.1:p.His275=
XM_017017547.2:c.825C=	XP_016873036.1:p.His275=
XM_017017548.2:c.*1755C=	XP_016873037.1:n.*1755C=
XM_017017549.2:c.*1529C=	XP_016873038.1:n.*1529C=
XM_024448437.1:c.*266C=	XP_024304205.1:n.*266C=
XM_024448438.1:c.738C=	XP_024304206.1:p.His246=
NM_014384.3:c.1119C= MANE Select	NP_055199.1:p.His373=