Canonical Allele Identifier: CA2010874961

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262799_134262824delinsAGCCGCAGCTTCGTCCCTTTCGGGGG , CM000673.2:g.134262799_134262824delinsAGCCGCAGCTTCGTCCCTTTCGGGGG	GRCh38
NC_000011.9:g.134132693_134132718delinsAGCCGCAGCTTCGTCCCTTTCGGGGG , CM000673.1:g.134132693_134132718delinsAGCCGCAGCTTCGTCCCTTTCGGGGG	GRCh37
NC_000011.8:g.133637903_133637928delinsAGCCGCAGCTTCGTCCCTTTCGGGGG	NCBI36
NG_015842.1:g.14260_14285delinsAGCCGCAGCTTCGTCCCTTTCGGGGG , LRG_448:g.14260_14285delinsAGCCGCAGCTTCGTCCCTTTCGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1195+177_1195+202delinsAGCCGCAGCTTCGTCCCTTTCGGGGG MANE Select	ENSP00000281182.5:n.1195+177_1195+202delinsAGCCGCAGCTTCGTCCCT...
ENST00000281182.8:c.1195+177_1195+202delinsAGCCGCAGCTTCGTCCCTTTCGGGGG	ENSP00000281182.4:n.1195+177_1195+202delinsAGCCGCAGCTTCGTCCCT...
ENST00000374752.6:c.814+177_814+202delinsAGCCGCAGCTTCGTCCCTTTCGGGGG	ENSP00000363884.4:n.814+177_814+202delinsAGCCGCAGCTTCGTCCCTTT...
ENST00000524502.2:n.225_250delinsAGCCGCAGCTTCGTCCCTTTCGGGGG
ENST00000526026.5:c.*914_*939delinsAGCCGCAGCTTCGTCCCTTTCGGGGG	ENSP00000431532.1:n.*914_*939delinsAGCCGCAGCTTCGTCCCTTTCGGGGG...
ENST00000531338.5:n.1616_1641delinsAGCCGCAGCTTCGTCCCTTTCGGGGG
ENST00000533387.5:n.2254+177_2254+202delinsAGCCGCAGCTTCGTCCCTTTCGGGGG
NM_014384.2:c.1195+177_1195+202delinsAGCCGCAGCTTCGTCCCTTTCGGGGG , LRG_448t1:c.1195+177_1195+202delinsAGCCGCAGCTTCGTCCCTTTCGGGGG	NP_055199.1:n.1195+177_1195+202delinsAGCCGCAGCTTCGTCCCTTTCGGG...
XM_005271501.2:c.1225_1250delinsAGCCGCAGCTTCGTCCCTTTCGGGGG	XP_005271558.1:p.Ser409=
XM_011542750.1:c.1195+177_1195+202delinsAGCCGCAGCTTCGTCCCTTTCGGGGG	XP_011541052.1:n.1195+177_1195+202delinsAGCCGCAGCTTCGTCCCTTTC...
XR_947819.1:n.1259+177_1259+202delinsAGCCGCAGCTTCGTCCCTTTCGGGGG
XR_947820.1:n.1824_1849delinsAGCCGCAGCTTCGTCCCTTTCGGGGG
XR_947822.1:n.1089+177_1089+202delinsAGCCGCAGCTTCGTCCCTTTCGGGGG
XR_947823.1:n.1245+177_1245+202delinsAGCCGCAGCTTCGTCCCTTTCGGGGG
XM_005271505.4:c.*1460+177_*1460+202delinsAGCCGCAGCTTCGTCCCTTTCGGGGG	XP_005271562.1:n.*1460+177_*1460+202delinsAGCCGCAGCTTCGTCCCTT...
XM_011542750.3:c.1195+177_1195+202delinsAGCCGCAGCTTCGTCCCTTTCGGGGG	XP_011541052.1:n.1195+177_1195+202delinsAGCCGCAGCTTCGTCCCTTTC...
XM_017017542.2:c.1195+177_1195+202delinsAGCCGCAGCTTCGTCCCTTTCGGGGG	XP_016873031.1:n.1195+177_1195+202delinsAGCCGCAGCTTCGTCCCTTTC...
XM_017017543.2:c.1225_1250delinsAGCCGCAGCTTCGTCCCTTTCGGGGG	XP_016873032.1:p.Ser409=
XM_017017544.2:c.*164+177_*164+202delinsAGCCGCAGCTTCGTCCCTTTCGGGGG	XP_016873033.1:n.*164+177_*164+202delinsAGCCGCAGCTTCGTCCCTTTC...
XM_017017545.2:c.*584_*609delinsAGCCGCAGCTTCGTCCCTTTCGGGGG	XP_016873034.1:n.*584_*609delinsAGCCGCAGCTTCGTCCCTTTCGGGGG
XM_017017546.2:c.901+177_901+202delinsAGCCGCAGCTTCGTCCCTTTCGGGGG	XP_016873035.1:n.901+177_901+202delinsAGCCGCAGCTTCGTCCCTTTCGG...
XM_017017547.2:c.901+177_901+202delinsAGCCGCAGCTTCGTCCCTTTCGGGGG	XP_016873036.1:n.901+177_901+202delinsAGCCGCAGCTTCGTCCCTTTCGG...
XM_017017548.2:c.*1861_*1886delinsAGCCGCAGCTTCGTCCCTTTCGGGGG	XP_016873037.1:n.*1861_*1886delinsAGCCGCAGCTTCGTCCCTTTCGGGGG
XM_017017549.2:c.*1605+177_*1605+202delinsAGCCGCAGCTTCGTCCCTTTCGGGGG	XP_016873038.1:n.*1605+177_*1605+202delinsAGCCGCAGCTTCGTCCCTT...
XM_024448437.1:c.*519_*544delinsAGCCGCAGCTTCGTCCCTTTCGGGGG	XP_024304205.1:n.*519_*544delinsAGCCGCAGCTTCGTCCCTTTCGGGGG
XM_024448438.1:c.814+177_814+202delinsAGCCGCAGCTTCGTCCCTTTCGGGGG	XP_024304206.1:n.814+177_814+202delinsAGCCGCAGCTTCGTCCCTTTCGG...
NM_014384.3:c.1195+177_1195+202delinsAGCCGCAGCTTCGTCCCTTTCGGGGG MANE Select	NP_055199.1:n.1195+177_1195+202delinsAGCCGCAGCTTCGTCCCTTTCGGG...