Canonical Allele Identifier: CA2010874607

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262598T= , CM000673.2:g.134262598T=	GRCh38
NC_000011.9:g.134132492T= , CM000673.1:g.134132492T=	GRCh37
NC_000011.8:g.133637702T=	NCBI36
NG_015842.1:g.14059T= , LRG_448:g.14059T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1171T= MANE Select	ENSP00000281182.5:p.Ser391=
ENST00000281182.8:c.1171T=	ENSP00000281182.4:p.Ser391=
ENST00000374752.6:c.790T=	ENSP00000363884.4:p.Ser264=
ENST00000524426.5:c.*901T=	ENSP00000431310.1:n.*901T=
ENST00000524502.2:n.171T=
ENST00000526026.5:c.*860T=	ENSP00000431532.1:n.*860T=
ENST00000531338.5:n.1415T=
ENST00000533387.5:n.2230T=
NM_014384.2:c.1171T= , LRG_448t1:c.1171T=	NP_055199.1:p.Ser391=
XM_005271501.2:c.1171T=	XP_005271558.1:p.Ser391=
XM_011542750.1:c.1171T=	XP_011541052.1:p.Ser391=
XR_947819.1:n.1235T=
XR_947820.1:n.1623T=
XR_947821.1:n.1380T=
XR_947822.1:n.1065T=
XR_947823.1:n.1221T=
XM_005271505.4:c.*1436T=	XP_005271562.1:n.*1436T=
XM_011542750.3:c.1171T=	XP_011541052.1:p.Ser391=
XM_017017542.2:c.1171T=	XP_016873031.1:p.Ser391=
XM_017017543.2:c.1171T=	XP_016873032.1:p.Ser391=
XM_017017544.2:c.*140T=	XP_016873033.1:n.*140T=
XM_017017545.2:c.*383T=	XP_016873034.1:n.*383T=
XM_017017546.2:c.877T=	XP_016873035.1:p.Ser293=
XM_017017547.2:c.877T=	XP_016873036.1:p.Ser293=
XM_017017548.2:c.*1807T=	XP_016873037.1:n.*1807T=
XM_017017549.2:c.*1581T=	XP_016873038.1:n.*1581T=
XM_024448437.1:c.*318T=	XP_024304205.1:n.*318T=
XM_024448438.1:c.790T=	XP_024304206.1:p.Ser264=
NM_014384.3:c.1171T= MANE Select	NP_055199.1:p.Ser391=