Canonical Allele Identifier: CA477723526

Gene: ACAD8

Linked Data

• MyVariant Identifiers: chr11:g.134132494C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262600C>A , CM000673.2:g.134262600C>A	GRCh38
NC_000011.9:g.134132494C>A , CM000673.1:g.134132494C>A	GRCh37
NC_000011.8:g.133637704C>A	NCBI36
NG_015842.1:g.14061C>A , LRG_448:g.14061C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1173C>A MANE Select	ENSP00000281182.5:p.Ser391=
ENST00000281182.8:c.1173C>A	ENSP00000281182.4:p.Ser391=
ENST00000374752.6:c.792C>A	ENSP00000363884.4:p.Ser264=
ENST00000524426.5:c.*903C>A	ENSP00000431310.1:n.*903C>A
ENST00000524502.2:n.173C>A
ENST00000526026.5:c.*862C>A	ENSP00000431532.1:n.*862C>A
ENST00000531338.5:n.1417C>A
ENST00000533387.5:n.2232C>A
NM_014384.2:c.1173C>A , LRG_448t1:c.1173C>A	NP_055199.1:p.Ser391=
XM_005271501.2:c.1173C>A	XP_005271558.1:p.Ser391=
XM_011542750.1:c.1173C>A	XP_011541052.1:p.Ser391=
XR_947819.1:n.1237C>A
XR_947820.1:n.1625C>A
XR_947821.1:n.1382C>A
XR_947822.1:n.1067C>A
XR_947823.1:n.1223C>A
XM_005271505.4:c.*1438C>A	XP_005271562.1:n.*1438C>A
XM_011542750.3:c.1173C>A	XP_011541052.1:p.Ser391=
XM_017017542.2:c.1173C>A	XP_016873031.1:p.Ser391=
XM_017017543.2:c.1173C>A	XP_016873032.1:p.Ser391=
XM_017017544.2:c.*142C>A	XP_016873033.1:n.*142C>A
XM_017017545.2:c.*385C>A	XP_016873034.1:n.*385C>A
XM_017017546.2:c.879C>A	XP_016873035.1:p.Ser293=
XM_017017547.2:c.879C>A	XP_016873036.1:p.Ser293=
XM_017017548.2:c.*1809C>A	XP_016873037.1:n.*1809C>A
XM_017017549.2:c.*1583C>A	XP_016873038.1:n.*1583C>A
XM_024448437.1:c.*320C>A	XP_024304205.1:n.*320C>A
XM_024448438.1:c.792C>A	XP_024304206.1:p.Ser264=
NM_014384.3:c.1173C>A MANE Select	NP_055199.1:p.Ser391=