Canonical Allele Identifier: CA2010875207

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262917_134262918delinsAG , CM000673.2:g.134262917_134262918delinsAG	GRCh38
NC_000011.9:g.134132811_134132812delinsAG , CM000673.1:g.134132811_134132812delinsAG	GRCh37
NC_000011.8:g.133638021_133638022delinsAG	NCBI36
NG_015842.1:g.14378_14379delinsAG , LRG_448:g.14378_14379delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1195+295_1195+296delinsAG MANE Select	ENSP00000281182.5:n.1195+295_1195+296delinsAG
ENST00000281182.8:c.1195+295_1195+296delinsAG	ENSP00000281182.4:n.1195+295_1195+296delinsAG
ENST00000374752.6:c.814+295_814+296delinsAG	ENSP00000363884.4:n.814+295_814+296delinsAG
ENST00000524502.2:n.343_344delinsAG
ENST00000526026.5:c.*1032_*1033delinsAG	ENSP00000431532.1:n.*1032_*1033delinsAG
ENST00000531338.5:n.1734_1735delinsAG
ENST00000533387.5:n.2254+295_2254+296delinsAG
NM_014384.2:c.1195+295_1195+296delinsAG , LRG_448t1:c.1195+295_1195+296delinsAG	NP_055199.1:n.1195+295_1195+296delinsAG
XM_005271501.2:c.*38_*39delinsAG	XP_005271558.1:n.*38_*39delinsAG
XM_011542750.1:c.1195+295_1195+296delinsAG	XP_011541052.1:n.1195+295_1195+296delinsAG
XR_947819.1:n.1259+295_1259+296delinsAG
XR_947820.1:n.1942_1943delinsAG
XR_947822.1:n.1089+295_1089+296delinsAG
XR_947823.1:n.1245+295_1245+296delinsAG
XM_005271505.4:c.*1460+295_*1460+296delinsAG	XP_005271562.1:n.*1460+295_*1460+296delinsAG
XM_011542750.3:c.1195+295_1195+296delinsAG	XP_011541052.1:n.1195+295_1195+296delinsAG
XM_017017542.2:c.1195+295_1195+296delinsAG	XP_016873031.1:n.1195+295_1195+296delinsAG
XM_017017543.2:c.*38_*39delinsAG	XP_016873032.1:n.*38_*39delinsAG
XM_017017544.2:c.*164+295_*164+296delinsAG	XP_016873033.1:n.*164+295_*164+296delinsAG
XM_017017545.2:c.*702_*703delinsAG	XP_016873034.1:n.*702_*703delinsAG
XM_017017546.2:c.901+295_901+296delinsAG	XP_016873035.1:n.901+295_901+296delinsAG
XM_017017547.2:c.901+295_901+296delinsAG	XP_016873036.1:n.901+295_901+296delinsAG
XM_017017548.2:c.*1979_*1980delinsAG	XP_016873037.1:n.*1979_*1980delinsAG
XM_017017549.2:c.*1605+295_*1605+296delinsAG	XP_016873038.1:n.*1605+295_*1605+296delinsAG
XM_024448437.1:c.*637_*638delinsAG	XP_024304205.1:n.*637_*638delinsAG
XM_024448438.1:c.814+295_814+296delinsAG	XP_024304206.1:n.814+295_814+296delinsAG
NM_014384.3:c.1195+295_1195+296delinsAG MANE Select	NP_055199.1:n.1195+295_1195+296delinsAG