Canonical Allele Identifier: CA477723307

Gene: ACAD8

Linked Data

• MyVariant Identifiers: chr11:g.134132434G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262540G>A , CM000673.2:g.134262540G>A	GRCh38
NC_000011.9:g.134132434G>A , CM000673.1:g.134132434G>A	GRCh37
NC_000011.8:g.133637644G>A	NCBI36
NG_015842.1:g.14001G>A , LRG_448:g.14001G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1113G>A MANE Select	ENSP00000281182.5:p.Gln371=
ENST00000281182.8:c.1113G>A	ENSP00000281182.4:p.Gln371=
ENST00000374752.6:c.732G>A	ENSP00000363884.4:p.Gln244=
ENST00000524426.5:c.*843G>A	ENSP00000431310.1:n.*843G>A
ENST00000524502.2:n.113G>A
ENST00000526026.5:c.*802G>A	ENSP00000431532.1:n.*802G>A
ENST00000531338.5:n.1357G>A
ENST00000533387.5:n.2172G>A
NM_014384.2:c.1113G>A , LRG_448t1:c.1113G>A	NP_055199.1:p.Gln371=
XM_005271501.2:c.1113G>A	XP_005271558.1:p.Gln371=
XM_011542750.1:c.1113G>A	XP_011541052.1:p.Gln371=
XR_947819.1:n.1177G>A
XR_947820.1:n.1565G>A
XR_947821.1:n.1322G>A
XR_947822.1:n.1007G>A
XR_947823.1:n.1163G>A
XM_005271505.4:c.*1378G>A	XP_005271562.1:n.*1378G>A
XM_011542750.3:c.1113G>A	XP_011541052.1:p.Gln371=
XM_017017542.2:c.1113G>A	XP_016873031.1:p.Gln371=
XM_017017543.2:c.1113G>A	XP_016873032.1:p.Gln371=
XM_017017544.2:c.*82G>A	XP_016873033.1:n.*82G>A
XM_017017545.2:c.*325G>A	XP_016873034.1:n.*325G>A
XM_017017546.2:c.819G>A	XP_016873035.1:p.Gln273=
XM_017017547.2:c.819G>A	XP_016873036.1:p.Gln273=
XM_017017548.2:c.*1749G>A	XP_016873037.1:n.*1749G>A
XM_017017549.2:c.*1523G>A	XP_016873038.1:n.*1523G>A
XM_024448437.1:c.*260G>A	XP_024304205.1:n.*260G>A
XM_024448438.1:c.732G>A	XP_024304206.1:p.Gln244=
NM_014384.3:c.1113G>A MANE Select	NP_055199.1:p.Gln371=