Canonical Allele Identifier: CA231279548

Gene: ACAD8

Linked Data

• dbSNP Id: rs773618005
• gnomAD v3: 11-134262369-A-G
• gnomAD v4: 11-134262369-A-G
• MyVariant Identifiers: chr11:g.134132263A>G (hg19) ; chr11:g.134262369A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262369A>G , CM000673.2:g.134262369A>G	GRCh38
NC_000011.9:g.134132263A>G , CM000673.1:g.134132263A>G	GRCh37
NC_000011.8:g.133637473A>G	NCBI36
NG_015842.1:g.13830A>G , LRG_448:g.13830A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1093-151A>G MANE Select	ENSP00000281182.5:n.1093-151A>G
ENST00000281182.8:c.1093-151A>G	ENSP00000281182.4:n.1093-151A>G
ENST00000374752.6:c.712-151A>G	ENSP00000363884.4:n.712-151A>G
ENST00000524426.5:c.*823-151A>G	ENSP00000431310.1:n.*823-151A>G
ENST00000524502.2:n.92+93A>G
ENST00000524547.5:n.696-151A>G
ENST00000526026.5:c.*782-151A>G	ENSP00000431532.1:n.*782-151A>G
ENST00000531338.5:n.1186A>G
ENST00000533387.5:n.2152-151A>G
NM_014384.2:c.1093-151A>G , LRG_448t1:c.1093-151A>G	NP_055199.1:n.1093-151A>G
XM_005271501.2:c.1093-151A>G	XP_005271558.1:n.1093-151A>G
XM_011542750.1:c.1093-151A>G	XP_011541052.1:n.1093-151A>G
XR_947819.1:n.1157-151A>G
XR_947820.1:n.1394A>G
XR_947821.1:n.1301+93A>G
XR_947822.1:n.987-151A>G
XR_947823.1:n.1143-151A>G
XM_005271505.4:c.*1358-151A>G	XP_005271562.1:n.*1358-151A>G
XM_011542750.3:c.1093-151A>G	XP_011541052.1:n.1093-151A>G
XM_017017542.2:c.1093-151A>G	XP_016873031.1:n.1093-151A>G
XM_017017543.2:c.1093-151A>G	XP_016873032.1:n.1093-151A>G
XM_017017544.2:c.*61+93A>G	XP_016873033.1:n.*61+93A>G
XM_017017545.2:c.*154A>G	XP_016873034.1:n.*154A>G
XM_017017546.2:c.799-151A>G	XP_016873035.1:n.799-151A>G
XM_017017547.2:c.799-151A>G	XP_016873036.1:n.799-151A>G
XM_017017548.2:c.*1728+93A>G	XP_016873037.1:n.*1728+93A>G
XM_017017549.2:c.*1502+93A>G	XP_016873038.1:n.*1502+93A>G
XM_024448437.1:c.*89A>G	XP_024304205.1:n.*89A>G
XM_024448438.1:c.712-151A>G	XP_024304206.1:n.712-151A>G
NM_014384.3:c.1093-151A>G MANE Select	NP_055199.1:n.1093-151A>G