Canonical Allele Identifier: CA2616917925

Gene: ACAD8

Linked Data

• gnomAD v4: 11-134262410-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262410T>A , CM000673.2:g.134262410T>A	GRCh38
NC_000011.9:g.134132304T>A , CM000673.1:g.134132304T>A	GRCh37
NC_000011.8:g.133637514T>A	NCBI36
NG_015842.1:g.13871T>A , LRG_448:g.13871T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1093-110T>A MANE Select	ENSP00000281182.5:n.1093-110T>A
ENST00000281182.8:c.1093-110T>A	ENSP00000281182.4:n.1093-110T>A
ENST00000374752.6:c.712-110T>A	ENSP00000363884.4:n.712-110T>A
ENST00000524426.5:c.*823-110T>A	ENSP00000431310.1:n.*823-110T>A
ENST00000524502.2:n.93-110T>A
ENST00000524547.5:n.696-110T>A
ENST00000526026.5:c.*782-110T>A	ENSP00000431532.1:n.*782-110T>A
ENST00000531338.5:n.1227T>A
ENST00000533387.5:n.2152-110T>A
NM_014384.2:c.1093-110T>A , LRG_448t1:c.1093-110T>A	NP_055199.1:n.1093-110T>A
XM_005271501.2:c.1093-110T>A	XP_005271558.1:n.1093-110T>A
XM_011542750.1:c.1093-110T>A	XP_011541052.1:n.1093-110T>A
XR_947819.1:n.1157-110T>A
XR_947820.1:n.1435T>A
XR_947821.1:n.1302-110T>A
XR_947822.1:n.987-110T>A
XR_947823.1:n.1143-110T>A
XM_005271505.4:c.*1358-110T>A	XP_005271562.1:n.*1358-110T>A
XM_011542750.3:c.1093-110T>A	XP_011541052.1:n.1093-110T>A
XM_017017542.2:c.1093-110T>A	XP_016873031.1:n.1093-110T>A
XM_017017543.2:c.1093-110T>A	XP_016873032.1:n.1093-110T>A
XM_017017544.2:c.*62-110T>A	XP_016873033.1:n.*62-110T>A
XM_017017545.2:c.*195T>A	XP_016873034.1:n.*195T>A
XM_017017546.2:c.799-110T>A	XP_016873035.1:n.799-110T>A
XM_017017547.2:c.799-110T>A	XP_016873036.1:n.799-110T>A
XM_017017548.2:c.*1729-110T>A	XP_016873037.1:n.*1729-110T>A
XM_017017549.2:c.*1503-110T>A	XP_016873038.1:n.*1503-110T>A
XM_024448437.1:c.*130T>A	XP_024304205.1:n.*130T>A
XM_024448438.1:c.712-110T>A	XP_024304206.1:n.712-110T>A
NM_014384.3:c.1093-110T>A MANE Select	NP_055199.1:n.1093-110T>A