Canonical Allele Identifier: CA2010874545

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262565_134262580delinsAAGGATTACGCTGTTC , CM000673.2:g.134262565_134262580delinsAAGGATTACGCTGTTC	GRCh38
NC_000011.9:g.134132459_134132474delinsAAGGATTACGCTGTTC , CM000673.1:g.134132459_134132474delinsAAGGATTACGCTGTTC	GRCh37
NC_000011.8:g.133637669_133637684delinsAAGGATTACGCTGTTC	NCBI36
NG_015842.1:g.14026_14041delinsAAGGATTACGCTGTTC , LRG_448:g.14026_14041delinsAAGGATTACGCTGTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1138_1153delinsAAGGATTACGCTGTTC MANE Select	ENSP00000281182.5:p.Lys380=
ENST00000281182.8:c.1138_1153delinsAAGGATTACGCTGTTC	ENSP00000281182.4:p.Lys380=
ENST00000374752.6:c.757_772delinsAAGGATTACGCTGTTC	ENSP00000363884.4:p.Lys253=
ENST00000524426.5:c.*868_*883delinsAAGGATTACGCTGTTC	ENSP00000431310.1:n.*868_*883delinsAAGGATTACGCTGTTC
ENST00000524502.2:n.138_153delinsAAGGATTACGCTGTTC
ENST00000526026.5:c.*827_*842delinsAAGGATTACGCTGTTC	ENSP00000431532.1:n.*827_*842delinsAAGGATTACGCTGTTC
ENST00000531338.5:n.1382_1397delinsAAGGATTACGCTGTTC
ENST00000533387.5:n.2197_2212delinsAAGGATTACGCTGTTC
NM_014384.2:c.1138_1153delinsAAGGATTACGCTGTTC , LRG_448t1:c.1138_1153delinsAAGGATTACGCTGTTC	NP_055199.1:p.Lys380=
XM_005271501.2:c.1138_1153delinsAAGGATTACGCTGTTC	XP_005271558.1:p.Lys380=
XM_011542750.1:c.1138_1153delinsAAGGATTACGCTGTTC	XP_011541052.1:p.Lys380=
XR_947819.1:n.1202_1217delinsAAGGATTACGCTGTTC
XR_947820.1:n.1590_1605delinsAAGGATTACGCTGTTC
XR_947821.1:n.1347_1362delinsAAGGATTACGCTGTTC
XR_947822.1:n.1032_1047delinsAAGGATTACGCTGTTC
XR_947823.1:n.1188_1203delinsAAGGATTACGCTGTTC
XM_005271505.4:c.*1403_*1418delinsAAGGATTACGCTGTTC	XP_005271562.1:n.*1403_*1418delinsAAGGATTACGCTGTTC
XM_011542750.3:c.1138_1153delinsAAGGATTACGCTGTTC	XP_011541052.1:p.Lys380=
XM_017017542.2:c.1138_1153delinsAAGGATTACGCTGTTC	XP_016873031.1:p.Lys380=
XM_017017543.2:c.1138_1153delinsAAGGATTACGCTGTTC	XP_016873032.1:p.Lys380=
XM_017017544.2:c.*107_*122delinsAAGGATTACGCTGTTC	XP_016873033.1:n.*107_*122delinsAAGGATTACGCTGTTC
XM_017017545.2:c.*350_*365delinsAAGGATTACGCTGTTC	XP_016873034.1:n.*350_*365delinsAAGGATTACGCTGTTC
XM_017017546.2:c.844_859delinsAAGGATTACGCTGTTC	XP_016873035.1:p.Lys282=
XM_017017547.2:c.844_859delinsAAGGATTACGCTGTTC	XP_016873036.1:p.Lys282=
XM_017017548.2:c.*1774_*1789delinsAAGGATTACGCTGTTC	XP_016873037.1:n.*1774_*1789delinsAAGGATTACGCTGTTC
XM_017017549.2:c.*1548_*1563delinsAAGGATTACGCTGTTC	XP_016873038.1:n.*1548_*1563delinsAAGGATTACGCTGTTC
XM_024448437.1:c.*285_*300delinsAAGGATTACGCTGTTC	XP_024304205.1:n.*285_*300delinsAAGGATTACGCTGTTC
XM_024448438.1:c.757_772delinsAAGGATTACGCTGTTC	XP_024304206.1:p.Lys253=
NM_014384.3:c.1138_1153delinsAAGGATTACGCTGTTC MANE Select	NP_055199.1:p.Lys380=