Canonical Allele Identifier: CA2616918127
Gene: ACAD8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134262462G>A , CM000673.2:g.134262462G>A GRCh38
NC_000011.9:g.134132356G>A , CM000673.1:g.134132356G>A GRCh37
NC_000011.8:g.133637566G>A NCBI36
NG_015842.1:g.13923G>A , LRG_448:g.13923G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000281182.9:c.1093-58G>A MANE Select ENSP00000281182.5:n.1093-58G>A
ENST00000281182.8:c.1093-58G>A ENSP00000281182.4:n.1093-58G>A
ENST00000374752.6:c.712-58G>A ENSP00000363884.4:n.712-58G>A
ENST00000524426.5:c.*823-58G>A ENSP00000431310.1:n.*823-58G>A
ENST00000524502.2:n.93-58G>A
ENST00000524547.5:n.696-58G>A
ENST00000526026.5:c.*782-58G>A ENSP00000431532.1:n.*782-58G>A
ENST00000531338.5:n.1279G>A
ENST00000533387.5:n.2152-58G>A
NM_014384.2:c.1093-58G>A , LRG_448t1:c.1093-58G>A NP_055199.1:n.1093-58G>A
XM_005271501.2:c.1093-58G>A XP_005271558.1:n.1093-58G>A
XM_011542750.1:c.1093-58G>A XP_011541052.1:n.1093-58G>A
XR_947819.1:n.1157-58G>A
XR_947820.1:n.1487G>A
XR_947821.1:n.1302-58G>A
XR_947822.1:n.987-58G>A
XR_947823.1:n.1143-58G>A
XM_005271505.4:c.*1358-58G>A XP_005271562.1:n.*1358-58G>A
XM_011542750.3:c.1093-58G>A XP_011541052.1:n.1093-58G>A
XM_017017542.2:c.1093-58G>A XP_016873031.1:n.1093-58G>A
XM_017017543.2:c.1093-58G>A XP_016873032.1:n.1093-58G>A
XM_017017544.2:c.*62-58G>A XP_016873033.1:n.*62-58G>A
XM_017017545.2:c.*247G>A XP_016873034.1:n.*247G>A
XM_017017546.2:c.799-58G>A XP_016873035.1:n.799-58G>A
XM_017017547.2:c.799-58G>A XP_016873036.1:n.799-58G>A
XM_017017548.2:c.*1729-58G>A XP_016873037.1:n.*1729-58G>A
XM_017017549.2:c.*1503-58G>A XP_016873038.1:n.*1503-58G>A
XM_024448437.1:c.*182G>A XP_024304205.1:n.*182G>A
XM_024448438.1:c.712-58G>A XP_024304206.1:n.712-58G>A
NM_014384.3:c.1093-58G>A MANE Select NP_055199.1:n.1093-58G>A