Canonical Allele Identifier: CA2010875171

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262892_134262893delinsGA , CM000673.2:g.134262892_134262893delinsGA	GRCh38
NC_000011.9:g.134132786_134132787delinsGA , CM000673.1:g.134132786_134132787delinsGA	GRCh37
NC_000011.8:g.133637996_133637997delinsGA	NCBI36
NG_015842.1:g.14353_14354delinsGA , LRG_448:g.14353_14354delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1195+270_1195+271delinsGA MANE Select	ENSP00000281182.5:n.1195+270_1195+271delinsGA
ENST00000281182.8:c.1195+270_1195+271delinsGA	ENSP00000281182.4:n.1195+270_1195+271delinsGA
ENST00000374752.6:c.814+270_814+271delinsGA	ENSP00000363884.4:n.814+270_814+271delinsGA
ENST00000524502.2:n.318_319delinsGA
ENST00000526026.5:c.*1007_*1008delinsGA	ENSP00000431532.1:n.*1007_*1008delinsGA
ENST00000531338.5:n.1709_1710delinsGA
ENST00000533387.5:n.2254+270_2254+271delinsGA
NM_014384.2:c.1195+270_1195+271delinsGA , LRG_448t1:c.1195+270_1195+271delinsGA	NP_055199.1:n.1195+270_1195+271delinsGA
XM_005271501.2:c.*13_*14delinsGA	XP_005271558.1:n.*13_*14delinsGA
XM_011542750.1:c.1195+270_1195+271delinsGA	XP_011541052.1:n.1195+270_1195+271delinsGA
XR_947819.1:n.1259+270_1259+271delinsGA
XR_947820.1:n.1917_1918delinsGA
XR_947822.1:n.1089+270_1089+271delinsGA
XR_947823.1:n.1245+270_1245+271delinsGA
XM_005271505.4:c.*1460+270_*1460+271delinsGA	XP_005271562.1:n.*1460+270_*1460+271delinsGA
XM_011542750.3:c.1195+270_1195+271delinsGA	XP_011541052.1:n.1195+270_1195+271delinsGA
XM_017017542.2:c.1195+270_1195+271delinsGA	XP_016873031.1:n.1195+270_1195+271delinsGA
XM_017017543.2:c.*13_*14delinsGA	XP_016873032.1:n.*13_*14delinsGA
XM_017017544.2:c.*164+270_*164+271delinsGA	XP_016873033.1:n.*164+270_*164+271delinsGA
XM_017017545.2:c.*677_*678delinsGA	XP_016873034.1:n.*677_*678delinsGA
XM_017017546.2:c.901+270_901+271delinsGA	XP_016873035.1:n.901+270_901+271delinsGA
XM_017017547.2:c.901+270_901+271delinsGA	XP_016873036.1:n.901+270_901+271delinsGA
XM_017017548.2:c.*1954_*1955delinsGA	XP_016873037.1:n.*1954_*1955delinsGA
XM_017017549.2:c.*1605+270_*1605+271delinsGA	XP_016873038.1:n.*1605+270_*1605+271delinsGA
XM_024448437.1:c.*612_*613delinsGA	XP_024304205.1:n.*612_*613delinsGA
XM_024448438.1:c.814+270_814+271delinsGA	XP_024304206.1:n.814+270_814+271delinsGA
NM_014384.3:c.1195+270_1195+271delinsGA MANE Select	NP_055199.1:n.1195+270_1195+271delinsGA