Canonical Allele Identifier: CA2010874338

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262399_134262400delinsGT , CM000673.2:g.134262399_134262400delinsGT	GRCh38
NC_000011.9:g.134132293_134132294delinsGT , CM000673.1:g.134132293_134132294delinsGT	GRCh37
NC_000011.8:g.133637503_133637504delinsGT	NCBI36
NG_015842.1:g.13860_13861delinsGT , LRG_448:g.13860_13861delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1093-121_1093-120delinsGT MANE Select	ENSP00000281182.5:n.1093-121_1093-120delinsGT
ENST00000281182.8:c.1093-121_1093-120delinsGT	ENSP00000281182.4:n.1093-121_1093-120delinsGT
ENST00000374752.6:c.712-121_712-120delinsGT	ENSP00000363884.4:n.712-121_712-120delinsGT
ENST00000524426.5:c.*823-121_*823-120delinsGT	ENSP00000431310.1:n.*823-121_*823-120delinsGT
ENST00000524502.2:n.93-121_93-120delinsGT
ENST00000524547.5:n.696-121_696-120delinsGT
ENST00000526026.5:c.*782-121_*782-120delinsGT	ENSP00000431532.1:n.*782-121_*782-120delinsGT
ENST00000531338.5:n.1216_1217delinsGT
ENST00000533387.5:n.2152-121_2152-120delinsGT
NM_014384.2:c.1093-121_1093-120delinsGT , LRG_448t1:c.1093-121_1093-120delinsGT	NP_055199.1:n.1093-121_1093-120delinsGT
XM_005271501.2:c.1093-121_1093-120delinsGT	XP_005271558.1:n.1093-121_1093-120delinsGT
XM_011542750.1:c.1093-121_1093-120delinsGT	XP_011541052.1:n.1093-121_1093-120delinsGT
XR_947819.1:n.1157-121_1157-120delinsGT
XR_947820.1:n.1424_1425delinsGT
XR_947821.1:n.1302-121_1302-120delinsGT
XR_947822.1:n.987-121_987-120delinsGT
XR_947823.1:n.1143-121_1143-120delinsGT
XM_005271505.4:c.*1358-121_*1358-120delinsGT	XP_005271562.1:n.*1358-121_*1358-120delinsGT
XM_011542750.3:c.1093-121_1093-120delinsGT	XP_011541052.1:n.1093-121_1093-120delinsGT
XM_017017542.2:c.1093-121_1093-120delinsGT	XP_016873031.1:n.1093-121_1093-120delinsGT
XM_017017543.2:c.1093-121_1093-120delinsGT	XP_016873032.1:n.1093-121_1093-120delinsGT
XM_017017544.2:c.*62-121_*62-120delinsGT	XP_016873033.1:n.*62-121_*62-120delinsGT
XM_017017545.2:c.*184_*185delinsGT	XP_016873034.1:n.*184_*185delinsGT
XM_017017546.2:c.799-121_799-120delinsGT	XP_016873035.1:n.799-121_799-120delinsGT
XM_017017547.2:c.799-121_799-120delinsGT	XP_016873036.1:n.799-121_799-120delinsGT
XM_017017548.2:c.*1729-121_*1729-120delinsGT	XP_016873037.1:n.*1729-121_*1729-120delinsGT
XM_017017549.2:c.*1503-121_*1503-120delinsGT	XP_016873038.1:n.*1503-121_*1503-120delinsGT
XM_024448437.1:c.*119_*120delinsGT	XP_024304205.1:n.*119_*120delinsGT
XM_024448438.1:c.712-121_712-120delinsGT	XP_024304206.1:n.712-121_712-120delinsGT
NM_014384.3:c.1093-121_1093-120delinsGT MANE Select	NP_055199.1:n.1093-121_1093-120delinsGT