Canonical Allele Identifier: CA2739353361

Gene: ACAD8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262813C>A , CM000673.2:g.134262813C>A	GRCh38
NC_000011.9:g.134132707C>A , CM000673.1:g.134132707C>A	GRCh37
NC_000011.8:g.133637917C>A	NCBI36
NG_015842.1:g.14274C>A , LRG_448:g.14274C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1195+191C>A MANE Select	ENSP00000281182.5:n.1195+191C>A
ENST00000281182.8:c.1195+191C>A	ENSP00000281182.4:n.1195+191C>A
ENST00000374752.6:c.814+191C>A	ENSP00000363884.4:n.814+191C>A
ENST00000524502.2:n.239C>A
ENST00000526026.5:c.*928C>A	ENSP00000431532.1:n.*928C>A
ENST00000531338.5:n.1630C>A
ENST00000533387.5:n.2254+191C>A
NM_014384.2:c.1195+191C>A , LRG_448t1:c.1195+191C>A	NP_055199.1:n.1195+191C>A
XM_005271501.2:c.1239C>A	XP_005271558.1:p.Val413=
XM_011542750.1:c.1195+191C>A	XP_011541052.1:n.1195+191C>A
XR_947819.1:n.1259+191C>A
XR_947820.1:n.1838C>A
XR_947822.1:n.1089+191C>A
XR_947823.1:n.1245+191C>A
XM_005271505.4:c.*1460+191C>A	XP_005271562.1:n.*1460+191C>A
XM_011542750.3:c.1195+191C>A	XP_011541052.1:n.1195+191C>A
XM_017017542.2:c.1195+191C>A	XP_016873031.1:n.1195+191C>A
XM_017017543.2:c.1239C>A	XP_016873032.1:p.Val413=
XM_017017544.2:c.*164+191C>A	XP_016873033.1:n.*164+191C>A
XM_017017545.2:c.*598C>A	XP_016873034.1:n.*598C>A
XM_017017546.2:c.901+191C>A	XP_016873035.1:n.901+191C>A
XM_017017547.2:c.901+191C>A	XP_016873036.1:n.901+191C>A
XM_017017548.2:c.*1875C>A	XP_016873037.1:n.*1875C>A
XM_017017549.2:c.*1605+191C>A	XP_016873038.1:n.*1605+191C>A
XM_024448437.1:c.*533C>A	XP_024304205.1:n.*533C>A
XM_024448438.1:c.814+191C>A	XP_024304206.1:n.814+191C>A
NM_014384.3:c.1195+191C>A MANE Select	NP_055199.1:n.1195+191C>A