Canonical Allele Identifier: CA477723259

Gene: ACAD8

Linked Data

• gnomAD v4: 11-134262528-C-T
• MyVariant Identifiers: chr11:g.134132422C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134262528C>T , CM000673.2:g.134262528C>T	GRCh38
NC_000011.9:g.134132422C>T , CM000673.1:g.134132422C>T	GRCh37
NC_000011.8:g.133637632C>T	NCBI36
NG_015842.1:g.13989C>T , LRG_448:g.13989C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281182.9:c.1101C>T MANE Select	ENSP00000281182.5:p.Asn367=
ENST00000281182.8:c.1101C>T	ENSP00000281182.4:p.Asn367=
ENST00000374752.6:c.720C>T	ENSP00000363884.4:p.Asn240=
ENST00000524426.5:c.*831C>T	ENSP00000431310.1:n.*831C>T
ENST00000524502.2:n.101C>T
ENST00000526026.5:c.*790C>T	ENSP00000431532.1:n.*790C>T
ENST00000531338.5:n.1345C>T
ENST00000533387.5:n.2160C>T
NM_014384.2:c.1101C>T , LRG_448t1:c.1101C>T	NP_055199.1:p.Asn367=
XM_005271501.2:c.1101C>T	XP_005271558.1:p.Asn367=
XM_011542750.1:c.1101C>T	XP_011541052.1:p.Asn367=
XR_947819.1:n.1165C>T
XR_947820.1:n.1553C>T
XR_947821.1:n.1310C>T
XR_947822.1:n.995C>T
XR_947823.1:n.1151C>T
XM_005271505.4:c.*1366C>T	XP_005271562.1:n.*1366C>T
XM_011542750.3:c.1101C>T	XP_011541052.1:p.Asn367=
XM_017017542.2:c.1101C>T	XP_016873031.1:p.Asn367=
XM_017017543.2:c.1101C>T	XP_016873032.1:p.Asn367=
XM_017017544.2:c.*70C>T	XP_016873033.1:n.*70C>T
XM_017017545.2:c.*313C>T	XP_016873034.1:n.*313C>T
XM_017017546.2:c.807C>T	XP_016873035.1:p.Asn269=
XM_017017547.2:c.807C>T	XP_016873036.1:p.Asn269=
XM_017017548.2:c.*1737C>T	XP_016873037.1:n.*1737C>T
XM_017017549.2:c.*1511C>T	XP_016873038.1:n.*1511C>T
XM_024448437.1:c.*248C>T	XP_024304205.1:n.*248C>T
XM_024448438.1:c.720C>T	XP_024304206.1:p.Asn240=
NM_014384.3:c.1101C>T MANE Select	NP_055199.1:p.Asn367=