Canonical Allele Identifier: CA383515678

Gene: ACAD8

Linked Data

• MyVariant Identifiers: chr11:g.134128492T>G (hg19) ; chr11:g.134258598T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134258598T>G , CM000673.2:g.134258598T>G	GRCh38
NC_000011.9:g.134128492T>G , CM000673.1:g.134128492T>G	GRCh37
NC_000011.8:g.133633702T>G	NCBI36
NG_015842.1:g.10059T>G , LRG_448:g.10059T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000281182.9:c.464T>G MANE Select	ENSP00000281182.5:p.Phe155Cys
ENST00000281182.8:c.464T>G	ENSP00000281182.4:p.Phe155Cys
ENST00000374752.6:c.110-410T>G	ENSP00000363884.4:n.110-410T>G
ENST00000524426.5:c.*63T>G	ENSP00000431310.1:n.*63T>G
ENST00000524547.5:n.94-410T>G
ENST00000526026.5:c.*153T>G	ENSP00000431532.1:n.*153T>G
ENST00000527082.5:n.318T>G
ENST00000527665.5:n.852T>G
ENST00000528325.5:n.293T>G
ENST00000530533.5:n.327T>G
ENST00000531338.5:n.320T>G
ENST00000533387.5:n.225T>G
ENST00000534240.5:n.225T>G
ENST00000534433.5:n.423-410T>G
NM_014384.2:c.464T>G , LRG_448t1:c.464T>G	NP_055199.1:p.Phe155Cys
XM_005271501.2:c.464T>G	XP_005271558.1:p.Phe155Cys
XM_005271505.2:c.464T>G	XP_005271562.1:p.Phe155Cys
XM_011542750.1:c.464T>G	XP_011541052.1:p.Phe155Cys
XR_947819.1:n.528T>G
XR_947820.1:n.528T>G
XR_947821.1:n.528T>G
XR_947822.1:n.358T>G
XR_947823.1:n.514T>G
XM_005271505.4:c.464T>G	XP_005271562.1:p.Phe155Cys
XM_011542750.3:c.464T>G	XP_011541052.1:p.Phe155Cys
XM_017017542.2:c.464T>G	XP_016873031.1:p.Phe155Cys
XM_017017543.2:c.464T>G	XP_016873032.1:p.Phe155Cys
XM_017017544.2:c.464T>G	XP_016873033.1:p.Phe155Cys
XM_017017545.2:c.464T>G	XP_016873034.1:p.Phe155Cys
XM_017017546.2:c.170T>G	XP_016873035.1:p.Phe57Cys
XM_017017547.2:c.170T>G	XP_016873036.1:p.Phe57Cys
XM_017017548.2:c.464T>G	XP_016873037.1:p.Phe155Cys
XM_017017549.2:c.464T>G	XP_016873038.1:p.Phe155Cys
XM_024448437.1:c.464T>G	XP_024304205.1:p.Phe155Cys
XM_024448438.1:c.83T>G	XP_024304206.1:p.Phe28Cys
NM_014384.3:c.464T>G MANE Select	NP_055199.1:p.Phe155Cys