Canonical Allele Identifier: CA2010874373

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262439_134262449delinsCGTGGGCTGGG , CM000673.2:g.134262439_134262449delinsCGTGGGCTGGG	GRCh38
NC_000011.9:g.134132333_134132343delinsCGTGGGCTGGG , CM000673.1:g.134132333_134132343delinsCGTGGGCTGGG	GRCh37
NC_000011.8:g.133637543_133637553delinsCGTGGGCTGGG	NCBI36
NG_015842.1:g.13900_13910delinsCGTGGGCTGGG , LRG_448:g.13900_13910delinsCGTGGGCTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1093-81_1093-71delinsCGTGGGCTGGG MANE Select	ENSP00000281182.5:n.1093-81_1093-71delinsCGTGGGCTGGG
ENST00000281182.8:c.1093-81_1093-71delinsCGTGGGCTGGG	ENSP00000281182.4:n.1093-81_1093-71delinsCGTGGGCTGGG
ENST00000374752.6:c.712-81_712-71delinsCGTGGGCTGGG	ENSP00000363884.4:n.712-81_712-71delinsCGTGGGCTGGG
ENST00000524426.5:c.*823-81_*823-71delinsCGTGGGCTGGG	ENSP00000431310.1:n.*823-81_*823-71delinsCGTGGGCTGGG
ENST00000524502.2:n.93-81_93-71delinsCGTGGGCTGGG
ENST00000524547.5:n.696-81_696-71delinsCGTGGGCTGGG
ENST00000526026.5:c.*782-81_*782-71delinsCGTGGGCTGGG	ENSP00000431532.1:n.*782-81_*782-71delinsCGTGGGCTGGG
ENST00000531338.5:n.1256_1266delinsCGTGGGCTGGG
ENST00000533387.5:n.2152-81_2152-71delinsCGTGGGCTGGG
NM_014384.2:c.1093-81_1093-71delinsCGTGGGCTGGG , LRG_448t1:c.1093-81_1093-71delinsCGTGGGCTGGG	NP_055199.1:n.1093-81_1093-71delinsCGTGGGCTGGG
XM_005271501.2:c.1093-81_1093-71delinsCGTGGGCTGGG	XP_005271558.1:n.1093-81_1093-71delinsCGTGGGCTGGG
XM_011542750.1:c.1093-81_1093-71delinsCGTGGGCTGGG	XP_011541052.1:n.1093-81_1093-71delinsCGTGGGCTGGG
XR_947819.1:n.1157-81_1157-71delinsCGTGGGCTGGG
XR_947820.1:n.1464_1474delinsCGTGGGCTGGG
XR_947821.1:n.1302-81_1302-71delinsCGTGGGCTGGG
XR_947822.1:n.987-81_987-71delinsCGTGGGCTGGG
XR_947823.1:n.1143-81_1143-71delinsCGTGGGCTGGG
XM_005271505.4:c.*1358-81_*1358-71delinsCGTGGGCTGGG	XP_005271562.1:n.*1358-81_*1358-71delinsCGTGGGCTGGG
XM_011542750.3:c.1093-81_1093-71delinsCGTGGGCTGGG	XP_011541052.1:n.1093-81_1093-71delinsCGTGGGCTGGG
XM_017017542.2:c.1093-81_1093-71delinsCGTGGGCTGGG	XP_016873031.1:n.1093-81_1093-71delinsCGTGGGCTGGG
XM_017017543.2:c.1093-81_1093-71delinsCGTGGGCTGGG	XP_016873032.1:n.1093-81_1093-71delinsCGTGGGCTGGG
XM_017017544.2:c.*62-81_*62-71delinsCGTGGGCTGGG	XP_016873033.1:n.*62-81_*62-71delinsCGTGGGCTGGG
XM_017017545.2:c.*224_*234delinsCGTGGGCTGGG	XP_016873034.1:n.*224_*234delinsCGTGGGCTGGG
XM_017017546.2:c.799-81_799-71delinsCGTGGGCTGGG	XP_016873035.1:n.799-81_799-71delinsCGTGGGCTGGG
XM_017017547.2:c.799-81_799-71delinsCGTGGGCTGGG	XP_016873036.1:n.799-81_799-71delinsCGTGGGCTGGG
XM_017017548.2:c.*1729-81_*1729-71delinsCGTGGGCTGGG	XP_016873037.1:n.*1729-81_*1729-71delinsCGTGGGCTGGG
XM_017017549.2:c.*1503-81_*1503-71delinsCGTGGGCTGGG	XP_016873038.1:n.*1503-81_*1503-71delinsCGTGGGCTGGG
XM_024448437.1:c.*159_*169delinsCGTGGGCTGGG	XP_024304205.1:n.*159_*169delinsCGTGGGCTGGG
XM_024448438.1:c.712-81_712-71delinsCGTGGGCTGGG	XP_024304206.1:n.712-81_712-71delinsCGTGGGCTGGG
NM_014384.3:c.1093-81_1093-71delinsCGTGGGCTGGG MANE Select	NP_055199.1:n.1093-81_1093-71delinsCGTGGGCTGGG