Canonical Allele Identifier: CA2010874566

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262574G= , CM000673.2:g.134262574G=	GRCh38
NC_000011.9:g.134132468G= , CM000673.1:g.134132468G=	GRCh37
NC_000011.8:g.133637678G=	NCBI36
NG_015842.1:g.14035G= , LRG_448:g.14035G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1147G= MANE Select	ENSP00000281182.5:p.Ala383=
ENST00000281182.8:c.1147G=	ENSP00000281182.4:p.Ala383=
ENST00000374752.6:c.766G=	ENSP00000363884.4:p.Ala256=
ENST00000524426.5:c.*877G=	ENSP00000431310.1:n.*877G=
ENST00000524502.2:n.147G=
ENST00000526026.5:c.*836G=	ENSP00000431532.1:n.*836G=
ENST00000531338.5:n.1391G=
ENST00000533387.5:n.2206G=
NM_014384.2:c.1147G= , LRG_448t1:c.1147G=	NP_055199.1:p.Ala383=
XM_005271501.2:c.1147G=	XP_005271558.1:p.Ala383=
XM_011542750.1:c.1147G=	XP_011541052.1:p.Ala383=
XR_947819.1:n.1211G=
XR_947820.1:n.1599G=
XR_947821.1:n.1356G=
XR_947822.1:n.1041G=
XR_947823.1:n.1197G=
XM_005271505.4:c.*1412G=	XP_005271562.1:n.*1412G=
XM_011542750.3:c.1147G=	XP_011541052.1:p.Ala383=
XM_017017542.2:c.1147G=	XP_016873031.1:p.Ala383=
XM_017017543.2:c.1147G=	XP_016873032.1:p.Ala383=
XM_017017544.2:c.*116G=	XP_016873033.1:n.*116G=
XM_017017545.2:c.*359G=	XP_016873034.1:n.*359G=
XM_017017546.2:c.853G=	XP_016873035.1:p.Ala285=
XM_017017547.2:c.853G=	XP_016873036.1:p.Ala285=
XM_017017548.2:c.*1783G=	XP_016873037.1:n.*1783G=
XM_017017549.2:c.*1557G=	XP_016873038.1:n.*1557G=
XM_024448437.1:c.*294G=	XP_024304205.1:n.*294G=
XM_024448438.1:c.766G=	XP_024304206.1:p.Ala256=
NM_014384.3:c.1147G= MANE Select	NP_055199.1:p.Ala383=