Canonical Allele Identifier: CA2010875261

Gene: ACAD8

Linked Data

• dbSNP Id: rs1939986075
• gnomAD v3: 11-134262958-AG-A
• gnomAD v4: 11-134262958-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262961del , CM000673.2:g.134262961del	GRCh38
NC_000011.9:g.134132855del , CM000673.1:g.134132855del	GRCh37
NC_000011.8:g.133638065del	NCBI36
NG_015842.1:g.14422del , LRG_448:g.14422del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1195+339del MANE Select	ENSP00000281182.5:n.1195+339del
ENST00000281182.8:c.1195+339del	ENSP00000281182.4:n.1195+339del
ENST00000374752.6:c.814+339del	ENSP00000363884.4:n.814+339del
ENST00000524502.2:n.387del
ENST00000531338.5:n.1778del
ENST00000533387.5:n.2254+339del
NM_014384.2:c.1195+339del , LRG_448t1:c.1195+339del	NP_055199.1:n.1195+339del
XM_005271501.2:c.*82del	XP_005271558.1:n.*82del
XM_011542750.1:c.1195+339del	XP_011541052.1:n.1195+339del
XR_947819.1:n.1259+339del
XR_947820.1:n.1986del
XR_947822.1:n.1089+339del
XR_947823.1:n.1245+339del
XM_005271505.4:c.*1460+339del	XP_005271562.1:n.*1460+339del
XM_011542750.3:c.1195+339del	XP_011541052.1:n.1195+339del
XM_017017542.2:c.1195+339del	XP_016873031.1:n.1195+339del
XM_017017543.2:c.*82del	XP_016873032.1:n.*82del
XM_017017544.2:c.*164+339del	XP_016873033.1:n.*164+339del
XM_017017545.2:c.*746del	XP_016873034.1:n.*746del
XM_017017546.2:c.901+339del	XP_016873035.1:n.901+339del
XM_017017547.2:c.901+339del	XP_016873036.1:n.901+339del
XM_017017548.2:c.*2023del	XP_016873037.1:n.*2023del
XM_017017549.2:c.*1605+339del	XP_016873038.1:n.*1605+339del
XM_024448437.1:c.*681del	XP_024304205.1:n.*681del
XM_024448438.1:c.814+339del	XP_024304206.1:n.814+339del
NM_014384.3:c.1195+339del MANE Select	NP_055199.1:n.1195+339del