Canonical Allele Identifier: CA2010874482

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262527A= , CM000673.2:g.134262527A=	GRCh38
NC_000011.9:g.134132421A= , CM000673.1:g.134132421A=	GRCh37
NC_000011.8:g.133637631A=	NCBI36
NG_015842.1:g.13988A= , LRG_448:g.13988A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1100A= MANE Select	ENSP00000281182.5:p.Asn367=
ENST00000281182.8:c.1100A=	ENSP00000281182.4:p.Asn367=
ENST00000374752.6:c.719A=	ENSP00000363884.4:p.Asn240=
ENST00000524426.5:c.*830A=	ENSP00000431310.1:n.*830A=
ENST00000524502.2:n.100A=
ENST00000524547.5:n.703A=
ENST00000526026.5:c.*789A=	ENSP00000431532.1:n.*789A=
ENST00000531338.5:n.1344A=
ENST00000533387.5:n.2159A=
NM_014384.2:c.1100A= , LRG_448t1:c.1100A=	NP_055199.1:p.Asn367=
XM_005271501.2:c.1100A=	XP_005271558.1:p.Asn367=
XM_011542750.1:c.1100A=	XP_011541052.1:p.Asn367=
XR_947819.1:n.1164A=
XR_947820.1:n.1552A=
XR_947821.1:n.1309A=
XR_947822.1:n.994A=
XR_947823.1:n.1150A=
XM_005271505.4:c.*1365A=	XP_005271562.1:n.*1365A=
XM_011542750.3:c.1100A=	XP_011541052.1:p.Asn367=
XM_017017542.2:c.1100A=	XP_016873031.1:p.Asn367=
XM_017017543.2:c.1100A=	XP_016873032.1:p.Asn367=
XM_017017544.2:c.*69A=	XP_016873033.1:n.*69A=
XM_017017545.2:c.*312A=	XP_016873034.1:n.*312A=
XM_017017546.2:c.806A=	XP_016873035.1:p.Asn269=
XM_017017547.2:c.806A=	XP_016873036.1:p.Asn269=
XM_017017548.2:c.*1736A=	XP_016873037.1:n.*1736A=
XM_017017549.2:c.*1510A=	XP_016873038.1:n.*1510A=
XM_024448437.1:c.*247A=	XP_024304205.1:n.*247A=
XM_024448438.1:c.719A=	XP_024304206.1:p.Asn240=
NM_014384.3:c.1100A= MANE Select	NP_055199.1:p.Asn367=