Canonical Allele Identifier: CA2577891553

Gene: ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909514A>G , CM000665.2:g.128909514A>G	GRCh38
NC_000003.11:g.128628357A>G , CM000665.1:g.128628357A>G	GRCh37
NC_000003.10:g.130111047A>G	NCBI36
NG_017064.1:g.35025A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1563+93A>G MANE Select	ENSP00000312618.7:n.1563+93A>G
ENST00000511325.2:n.1734A>G
ENST00000679399.1:c.*1734+93A>G	ENSP00000505434.1:n.*1734+93A>G
ENST00000679431.1:c.*1439+93A>G	ENSP00000506440.1:n.*1439+93A>G
ENST00000679613.1:c.1563+93A>G	ENSP00000504971.1:n.1563+93A>G
ENST00000679715.1:c.1194+93A>G	ENSP00000506228.1:n.1194+93A>G
ENST00000679824.1:c.*2869+93A>G	ENSP00000505516.1:n.*2869+93A>G
ENST00000679990.1:n.1891A>G
ENST00000680636.1:c.1563+93A>G	ENSP00000504886.1:n.1563+93A>G
ENST00000680638.1:n.1409A>G
ENST00000680744.1:c.*916+93A>G	ENSP00000505243.1:n.*916+93A>G
ENST00000680764.1:c.*2967+93A>G	ENSP00000505126.1:n.*2967+93A>G
ENST00000681319.1:n.2349+93A>G
ENST00000681367.1:c.1563+93A>G	ENSP00000505309.1:n.1563+93A>G
ENST00000681552.1:c.1150-2993A>G	ENSP00000505699.1:n.1150-2993A>G
ENST00000681583.1:c.1563+93A>G	ENSP00000506340.1:n.1563+93A>G
ENST00000681585.1:c.*182+93A>G	ENSP00000506316.1:n.*182+93A>G
ENST00000681784.1:n.1734A>G
ENST00000681886.1:c.*849A>G	ENSP00000506500.1:n.*849A>G
ENST00000308982.11:c.1563+93A>G	ENSP00000312618.7:n.1563+93A>G
ENST00000505867.5:c.*1363+93A>G	ENSP00000425346.1:n.*1363+93A>G
ENST00000508971.1:c.852+93A>G	ENSP00000422683.1:n.852+93A>G
ENST00000511227.5:c.*1457+93A>G	ENSP00000425226.1:n.*1457+93A>G
ENST00000511325.1:n.637A>G
ENST00000511526.5:n.1096+93A>G
NM_014049.4:c.1563+93A>G	NP_054768.2:n.1563+93A>G
NR_033426.1:n.1941+93A>G
XM_011512742.1:c.1194+93A>G	XP_011511044.1:n.1194+93A>G
XM_024453484.1:c.1194+93A>G	XP_024309252.1:n.1194+93A>G
XM_024453485.1:c.1194+93A>G	XP_024309253.1:n.1194+93A>G
XR_427367.3:n.1639+93A>G
NM_014049.5:c.1563+93A>G MANE Select	NP_054768.2:n.1563+93A>G
NR_033426.2:n.1811+93A>G