Canonical Allele Identifier: CA2010874559

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262570_134262583delinsTTACGCTGTTCAGC , CM000673.2:g.134262570_134262583delinsTTACGCTGTTCAGC	GRCh38
NC_000011.9:g.134132464_134132477delinsTTACGCTGTTCAGC , CM000673.1:g.134132464_134132477delinsTTACGCTGTTCAGC	GRCh37
NC_000011.8:g.133637674_133637687delinsTTACGCTGTTCAGC	NCBI36
NG_015842.1:g.14031_14044delinsTTACGCTGTTCAGC , LRG_448:g.14031_14044delinsTTACGCTGTTCAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1143_1156delinsTTACGCTGTTCAGC MANE Select	ENSP00000281182.5:p.Asp381=
ENST00000281182.8:c.1143_1156delinsTTACGCTGTTCAGC	ENSP00000281182.4:p.Asp381=
ENST00000374752.6:c.762_775delinsTTACGCTGTTCAGC	ENSP00000363884.4:p.Asp254=
ENST00000524426.5:c.*873_*886delinsTTACGCTGTTCAGC	ENSP00000431310.1:n.*873_*886delinsTTACGCTGTTCAGC
ENST00000524502.2:n.143_156delinsTTACGCTGTTCAGC
ENST00000526026.5:c.*832_*845delinsTTACGCTGTTCAGC	ENSP00000431532.1:n.*832_*845delinsTTACGCTGTTCAGC
ENST00000531338.5:n.1387_1400delinsTTACGCTGTTCAGC
ENST00000533387.5:n.2202_2215delinsTTACGCTGTTCAGC
NM_014384.2:c.1143_1156delinsTTACGCTGTTCAGC , LRG_448t1:c.1143_1156delinsTTACGCTGTTCAGC	NP_055199.1:p.Asp381=
XM_005271501.2:c.1143_1156delinsTTACGCTGTTCAGC	XP_005271558.1:p.Asp381=
XM_011542750.1:c.1143_1156delinsTTACGCTGTTCAGC	XP_011541052.1:p.Asp381=
XR_947819.1:n.1207_1220delinsTTACGCTGTTCAGC
XR_947820.1:n.1595_1608delinsTTACGCTGTTCAGC
XR_947821.1:n.1352_1365delinsTTACGCTGTTCAGC
XR_947822.1:n.1037_1050delinsTTACGCTGTTCAGC
XR_947823.1:n.1193_1206delinsTTACGCTGTTCAGC
XM_005271505.4:c.*1408_*1421delinsTTACGCTGTTCAGC	XP_005271562.1:n.*1408_*1421delinsTTACGCTGTTCAGC
XM_011542750.3:c.1143_1156delinsTTACGCTGTTCAGC	XP_011541052.1:p.Asp381=
XM_017017542.2:c.1143_1156delinsTTACGCTGTTCAGC	XP_016873031.1:p.Asp381=
XM_017017543.2:c.1143_1156delinsTTACGCTGTTCAGC	XP_016873032.1:p.Asp381=
XM_017017544.2:c.*112_*125delinsTTACGCTGTTCAGC	XP_016873033.1:n.*112_*125delinsTTACGCTGTTCAGC
XM_017017545.2:c.*355_*368delinsTTACGCTGTTCAGC	XP_016873034.1:n.*355_*368delinsTTACGCTGTTCAGC
XM_017017546.2:c.849_862delinsTTACGCTGTTCAGC	XP_016873035.1:p.Asp283=
XM_017017547.2:c.849_862delinsTTACGCTGTTCAGC	XP_016873036.1:p.Asp283=
XM_017017548.2:c.*1779_*1792delinsTTACGCTGTTCAGC	XP_016873037.1:n.*1779_*1792delinsTTACGCTGTTCAGC
XM_017017549.2:c.*1553_*1566delinsTTACGCTGTTCAGC	XP_016873038.1:n.*1553_*1566delinsTTACGCTGTTCAGC
XM_024448437.1:c.*290_*303delinsTTACGCTGTTCAGC	XP_024304205.1:n.*290_*303delinsTTACGCTGTTCAGC
XM_024448438.1:c.762_775delinsTTACGCTGTTCAGC	XP_024304206.1:p.Asp254=
NM_014384.3:c.1143_1156delinsTTACGCTGTTCAGC MANE Select	NP_055199.1:p.Asp381=