Canonical Allele Identifier: CA2575035337

Gene: ACAD8

Linked Data

• gnomAD v4: 11-134262959-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262959G>A , CM000673.2:g.134262959G>A	GRCh38
NC_000011.9:g.134132853G>A , CM000673.1:g.134132853G>A	GRCh37
NC_000011.8:g.133638063G>A	NCBI36
NG_015842.1:g.14420G>A , LRG_448:g.14420G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1195+337G>A MANE Select	ENSP00000281182.5:n.1195+337G>A
ENST00000281182.8:c.1195+337G>A	ENSP00000281182.4:n.1195+337G>A
ENST00000374752.6:c.814+337G>A	ENSP00000363884.4:n.814+337G>A
ENST00000524502.2:n.385G>A
ENST00000531338.5:n.1776G>A
ENST00000533387.5:n.2254+337G>A
NM_014384.2:c.1195+337G>A , LRG_448t1:c.1195+337G>A	NP_055199.1:n.1195+337G>A
XM_005271501.2:c.*80G>A	XP_005271558.1:n.*80G>A
XM_011542750.1:c.1195+337G>A	XP_011541052.1:n.1195+337G>A
XR_947819.1:n.1259+337G>A
XR_947820.1:n.1984G>A
XR_947822.1:n.1089+337G>A
XR_947823.1:n.1245+337G>A
XM_005271505.4:c.*1460+337G>A	XP_005271562.1:n.*1460+337G>A
XM_011542750.3:c.1195+337G>A	XP_011541052.1:n.1195+337G>A
XM_017017542.2:c.1195+337G>A	XP_016873031.1:n.1195+337G>A
XM_017017543.2:c.*80G>A	XP_016873032.1:n.*80G>A
XM_017017544.2:c.*164+337G>A	XP_016873033.1:n.*164+337G>A
XM_017017545.2:c.*744G>A	XP_016873034.1:n.*744G>A
XM_017017546.2:c.901+337G>A	XP_016873035.1:n.901+337G>A
XM_017017547.2:c.901+337G>A	XP_016873036.1:n.901+337G>A
XM_017017548.2:c.*2021G>A	XP_016873037.1:n.*2021G>A
XM_017017549.2:c.*1605+337G>A	XP_016873038.1:n.*1605+337G>A
XM_024448437.1:c.*679G>A	XP_024304205.1:n.*679G>A
XM_024448438.1:c.814+337G>A	XP_024304206.1:n.814+337G>A
NM_014384.3:c.1195+337G>A MANE Select	NP_055199.1:n.1195+337G>A