Canonical Allele Identifier: CA2010874197

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262317_134262318delinsTG , CM000673.2:g.134262317_134262318delinsTG	GRCh38
NC_000011.9:g.134132211_134132212delinsTG , CM000673.1:g.134132211_134132212delinsTG	GRCh37
NC_000011.8:g.133637421_133637422delinsTG	NCBI36
NG_015842.1:g.13778_13779delinsTG , LRG_448:g.13778_13779delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1093-203_1093-202delinsTG MANE Select	ENSP00000281182.5:n.1093-203_1093-202delinsTG
ENST00000281182.8:c.1093-203_1093-202delinsTG	ENSP00000281182.4:n.1093-203_1093-202delinsTG
ENST00000374752.6:c.712-203_712-202delinsTG	ENSP00000363884.4:n.712-203_712-202delinsTG
ENST00000524426.5:c.*823-203_*823-202delinsTG	ENSP00000431310.1:n.*823-203_*823-202delinsTG
ENST00000524502.2:n.92+41_92+42delinsTG
ENST00000524547.5:n.696-203_696-202delinsTG
ENST00000526026.5:c.*782-203_*782-202delinsTG	ENSP00000431532.1:n.*782-203_*782-202delinsTG
ENST00000531338.5:n.1134_1135delinsTG
ENST00000533387.5:n.2152-203_2152-202delinsTG
NM_014384.2:c.1093-203_1093-202delinsTG , LRG_448t1:c.1093-203_1093-202delinsTG	NP_055199.1:n.1093-203_1093-202delinsTG
XM_005271501.2:c.1093-203_1093-202delinsTG	XP_005271558.1:n.1093-203_1093-202delinsTG
XM_011542750.1:c.1093-203_1093-202delinsTG	XP_011541052.1:n.1093-203_1093-202delinsTG
XR_947819.1:n.1157-203_1157-202delinsTG
XR_947820.1:n.1342_1343delinsTG
XR_947821.1:n.1301+41_1301+42delinsTG
XR_947822.1:n.987-203_987-202delinsTG
XR_947823.1:n.1143-203_1143-202delinsTG
XM_005271505.4:c.*1358-203_*1358-202delinsTG	XP_005271562.1:n.*1358-203_*1358-202delinsTG
XM_011542750.3:c.1093-203_1093-202delinsTG	XP_011541052.1:n.1093-203_1093-202delinsTG
XM_017017542.2:c.1093-203_1093-202delinsTG	XP_016873031.1:n.1093-203_1093-202delinsTG
XM_017017543.2:c.1093-203_1093-202delinsTG	XP_016873032.1:n.1093-203_1093-202delinsTG
XM_017017544.2:c.*61+41_*61+42delinsTG	XP_016873033.1:n.*61+41_*61+42delinsTG
XM_017017545.2:c.*102_*103delinsTG	XP_016873034.1:n.*102_*103delinsTG
XM_017017546.2:c.799-203_799-202delinsTG	XP_016873035.1:n.799-203_799-202delinsTG
XM_017017547.2:c.799-203_799-202delinsTG	XP_016873036.1:n.799-203_799-202delinsTG
XM_017017548.2:c.*1728+41_*1728+42delinsTG	XP_016873037.1:n.*1728+41_*1728+42delinsTG
XM_017017549.2:c.*1502+41_*1502+42delinsTG	XP_016873038.1:n.*1502+41_*1502+42delinsTG
XM_024448437.1:c.*37_*38delinsTG	XP_024304205.1:n.*37_*38delinsTG
XM_024448438.1:c.712-203_712-202delinsTG	XP_024304206.1:n.712-203_712-202delinsTG
NM_014384.3:c.1093-203_1093-202delinsTG MANE Select	NP_055199.1:n.1093-203_1093-202delinsTG