Canonical Allele Identifier: CA383518932

Gene: ACAD8

Linked Data

• MyVariant Identifiers: chr11:g.134132417T>A (hg19) ; chr11:g.134262523T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262523T>A , CM000673.2:g.134262523T>A	GRCh38
NC_000011.9:g.134132417T>A , CM000673.1:g.134132417T>A	GRCh37
NC_000011.8:g.133637627T>A	NCBI36
NG_015842.1:g.13984T>A , LRG_448:g.13984T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1096T>A MANE Select	ENSP00000281182.5:p.Cys366Ser
ENST00000281182.8:c.1096T>A	ENSP00000281182.4:p.Cys366Ser
ENST00000374752.6:c.715T>A	ENSP00000363884.4:p.Cys239Ser
ENST00000524426.5:c.*826T>A	ENSP00000431310.1:n.*826T>A
ENST00000524502.2:n.96T>A
ENST00000524547.5:n.699T>A
ENST00000526026.5:c.*785T>A	ENSP00000431532.1:n.*785T>A
ENST00000531338.5:n.1340T>A
ENST00000533387.5:n.2155T>A
NM_014384.2:c.1096T>A , LRG_448t1:c.1096T>A	NP_055199.1:p.Cys366Ser
XM_005271501.2:c.1096T>A	XP_005271558.1:p.Cys366Ser
XM_011542750.1:c.1096T>A	XP_011541052.1:p.Cys366Ser
XR_947819.1:n.1160T>A
XR_947820.1:n.1548T>A
XR_947821.1:n.1305T>A
XR_947822.1:n.990T>A
XR_947823.1:n.1146T>A
XM_005271505.4:c.*1361T>A	XP_005271562.1:n.*1361T>A
XM_011542750.3:c.1096T>A	XP_011541052.1:p.Cys366Ser
XM_017017542.2:c.1096T>A	XP_016873031.1:p.Cys366Ser
XM_017017543.2:c.1096T>A	XP_016873032.1:p.Cys366Ser
XM_017017544.2:c.*65T>A	XP_016873033.1:n.*65T>A
XM_017017545.2:c.*308T>A	XP_016873034.1:n.*308T>A
XM_017017546.2:c.802T>A	XP_016873035.1:p.Cys268Ser
XM_017017547.2:c.802T>A	XP_016873036.1:p.Cys268Ser
XM_017017548.2:c.*1732T>A	XP_016873037.1:n.*1732T>A
XM_017017549.2:c.*1506T>A	XP_016873038.1:n.*1506T>A
XM_024448437.1:c.*243T>A	XP_024304205.1:n.*243T>A
XM_024448438.1:c.715T>A	XP_024304206.1:p.Cys239Ser
NM_014384.3:c.1096T>A MANE Select	NP_055199.1:p.Cys366Ser