Canonical Allele Identifier: CA1400926966

Gene: ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909483_128909486delinsGACT , CM000665.2:g.128909483_128909486delinsGACT	GRCh38
NC_000003.11:g.128628326_128628329delinsGACT , CM000665.1:g.128628326_128628329delinsGACT	GRCh37
NC_000003.10:g.130111016_130111019delinsGACT	NCBI36
NG_017064.1:g.34994_34997delinsGACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1563+62_1563+65delinsGACT MANE Select	ENSP00000312618.7:n.1563+62_1563+65delinsGACT
ENST00000511325.2:n.1703_1706delinsGACT
ENST00000679399.1:c.*1734+62_*1734+65delinsGACT	ENSP00000505434.1:n.*1734+62_*1734+65delinsGACT
ENST00000679431.1:c.*1439+62_*1439+65delinsGACT	ENSP00000506440.1:n.*1439+62_*1439+65delinsGACT
ENST00000679613.1:c.1563+62_1563+65delinsGACT	ENSP00000504971.1:n.1563+62_1563+65delinsGACT
ENST00000679715.1:c.1194+62_1194+65delinsGACT	ENSP00000506228.1:n.1194+62_1194+65delinsGACT
ENST00000679824.1:c.*2869+62_*2869+65delinsGACT	ENSP00000505516.1:n.*2869+62_*2869+65delinsGACT
ENST00000679990.1:n.1860_1863delinsGACT
ENST00000680636.1:c.1563+62_1563+65delinsGACT	ENSP00000504886.1:n.1563+62_1563+65delinsGACT
ENST00000680638.1:n.1378_1381delinsGACT
ENST00000680744.1:c.*916+62_*916+65delinsGACT	ENSP00000505243.1:n.*916+62_*916+65delinsGACT
ENST00000680764.1:c.*2967+62_*2967+65delinsGACT	ENSP00000505126.1:n.*2967+62_*2967+65delinsGACT
ENST00000681319.1:n.2349+62_2349+65delinsGACT
ENST00000681367.1:c.1563+62_1563+65delinsGACT	ENSP00000505309.1:n.1563+62_1563+65delinsGACT
ENST00000681552.1:c.1150-3024_1150-3021delinsGACT	ENSP00000505699.1:n.1150-3024_1150-3021delinsGACT
ENST00000681583.1:c.1563+62_1563+65delinsGACT	ENSP00000506340.1:n.1563+62_1563+65delinsGACT
ENST00000681585.1:c.*182+62_*182+65delinsGACT	ENSP00000506316.1:n.*182+62_*182+65delinsGACT
ENST00000681784.1:n.1703_1706delinsGACT
ENST00000681886.1:c.*818_*821delinsGACT	ENSP00000506500.1:n.*818_*821delinsGACT
ENST00000308982.11:c.1563+62_1563+65delinsGACT	ENSP00000312618.7:n.1563+62_1563+65delinsGACT
ENST00000505867.5:c.*1363+62_*1363+65delinsGACT	ENSP00000425346.1:n.*1363+62_*1363+65delinsGACT
ENST00000508971.1:c.852+62_852+65delinsGACT	ENSP00000422683.1:n.852+62_852+65delinsGACT
ENST00000511227.5:c.*1457+62_*1457+65delinsGACT	ENSP00000425226.1:n.*1457+62_*1457+65delinsGACT
ENST00000511325.1:n.606_609delinsGACT
ENST00000511526.5:n.1096+62_1096+65delinsGACT
NM_014049.4:c.1563+62_1563+65delinsGACT	NP_054768.2:n.1563+62_1563+65delinsGACT
NR_033426.1:n.1941+62_1941+65delinsGACT
XM_011512742.1:c.1194+62_1194+65delinsGACT	XP_011511044.1:n.1194+62_1194+65delinsGACT
XM_024453484.1:c.1194+62_1194+65delinsGACT	XP_024309252.1:n.1194+62_1194+65delinsGACT
XM_024453485.1:c.1194+62_1194+65delinsGACT	XP_024309253.1:n.1194+62_1194+65delinsGACT
XR_427367.3:n.1639+62_1639+65delinsGACT
NM_014049.5:c.1563+62_1563+65delinsGACT MANE Select	NP_054768.2:n.1563+62_1563+65delinsGACT
NR_033426.2:n.1811+62_1811+65delinsGACT