Canonical Allele Identifier: CA2010875185

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262901G= , CM000673.2:g.134262901G=	GRCh38
NC_000011.9:g.134132795G= , CM000673.1:g.134132795G=	GRCh37
NC_000011.8:g.133638005G=	NCBI36
NG_015842.1:g.14362G= , LRG_448:g.14362G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1195+279G= MANE Select	ENSP00000281182.5:n.1195+279G=
ENST00000281182.8:c.1195+279G=	ENSP00000281182.4:n.1195+279G=
ENST00000374752.6:c.814+279G=	ENSP00000363884.4:n.814+279G=
ENST00000524502.2:n.327G=
ENST00000526026.5:c.*1016G=	ENSP00000431532.1:n.*1016G=
ENST00000531338.5:n.1718G=
ENST00000533387.5:n.2254+279G=
NM_014384.2:c.1195+279G= , LRG_448t1:c.1195+279G=	NP_055199.1:n.1195+279G=
XM_005271501.2:c.*22G=	XP_005271558.1:n.*22G=
XM_011542750.1:c.1195+279G=	XP_011541052.1:n.1195+279G=
XR_947819.1:n.1259+279G=
XR_947820.1:n.1926G=
XR_947822.1:n.1089+279G=
XR_947823.1:n.1245+279G=
XM_005271505.4:c.*1460+279G=	XP_005271562.1:n.*1460+279G=
XM_011542750.3:c.1195+279G=	XP_011541052.1:n.1195+279G=
XM_017017542.2:c.1195+279G=	XP_016873031.1:n.1195+279G=
XM_017017543.2:c.*22G=	XP_016873032.1:n.*22G=
XM_017017544.2:c.*164+279G=	XP_016873033.1:n.*164+279G=
XM_017017545.2:c.*686G=	XP_016873034.1:n.*686G=
XM_017017546.2:c.901+279G=	XP_016873035.1:n.901+279G=
XM_017017547.2:c.901+279G=	XP_016873036.1:n.901+279G=
XM_017017548.2:c.*1963G=	XP_016873037.1:n.*1963G=
XM_017017549.2:c.*1605+279G=	XP_016873038.1:n.*1605+279G=
XM_024448437.1:c.*621G=	XP_024304205.1:n.*621G=
XM_024448438.1:c.814+279G=	XP_024304206.1:n.814+279G=
NM_014384.3:c.1195+279G= MANE Select	NP_055199.1:n.1195+279G=