Canonical Allele Identifier: CA2010874587

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262584A= , CM000673.2:g.134262584A=	GRCh38
NC_000011.9:g.134132478A= , CM000673.1:g.134132478A=	GRCh37
NC_000011.8:g.133637688A=	NCBI36
NG_015842.1:g.14045A= , LRG_448:g.14045A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1157A= MANE Select	ENSP00000281182.5:p.Gln386=
ENST00000281182.8:c.1157A=	ENSP00000281182.4:p.Gln386=
ENST00000374752.6:c.776A=	ENSP00000363884.4:p.Gln259=
ENST00000524426.5:c.*887A=	ENSP00000431310.1:n.*887A=
ENST00000524502.2:n.157A=
ENST00000526026.5:c.*846A=	ENSP00000431532.1:n.*846A=
ENST00000531338.5:n.1401A=
ENST00000533387.5:n.2216A=
NM_014384.2:c.1157A= , LRG_448t1:c.1157A=	NP_055199.1:p.Gln386=
XM_005271501.2:c.1157A=	XP_005271558.1:p.Gln386=
XM_011542750.1:c.1157A=	XP_011541052.1:p.Gln386=
XR_947819.1:n.1221A=
XR_947820.1:n.1609A=
XR_947821.1:n.1366A=
XR_947822.1:n.1051A=
XR_947823.1:n.1207A=
XM_005271505.4:c.*1422A=	XP_005271562.1:n.*1422A=
XM_011542750.3:c.1157A=	XP_011541052.1:p.Gln386=
XM_017017542.2:c.1157A=	XP_016873031.1:p.Gln386=
XM_017017543.2:c.1157A=	XP_016873032.1:p.Gln386=
XM_017017544.2:c.*126A=	XP_016873033.1:n.*126A=
XM_017017545.2:c.*369A=	XP_016873034.1:n.*369A=
XM_017017546.2:c.863A=	XP_016873035.1:p.Gln288=
XM_017017547.2:c.863A=	XP_016873036.1:p.Gln288=
XM_017017548.2:c.*1793A=	XP_016873037.1:n.*1793A=
XM_017017549.2:c.*1567A=	XP_016873038.1:n.*1567A=
XM_024448437.1:c.*304A=	XP_024304205.1:n.*304A=
XM_024448438.1:c.776A=	XP_024304206.1:p.Gln259=
NM_014384.3:c.1157A= MANE Select	NP_055199.1:p.Gln386=