Canonical Allele Identifier: CA1400926957

Gene: ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909471_128909483delinsCAGCATTCATGAG , CM000665.2:g.128909471_128909483delinsCAGCATTCATGAG	GRCh38
NC_000003.11:g.128628314_128628326delinsCAGCATTCATGAG , CM000665.1:g.128628314_128628326delinsCAGCATTCATGAG	GRCh37
NC_000003.10:g.130111004_130111016delinsCAGCATTCATGAG	NCBI36
NG_017064.1:g.34982_34994delinsCAGCATTCATGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1563+50_1563+62delinsCAGCATTCATGAG MANE Select	ENSP00000312618.7:n.1563+50_1563+62delinsCAGCATTCATGAG
ENST00000511325.2:n.1691_1703delinsCAGCATTCATGAG
ENST00000679399.1:c.*1734+50_*1734+62delinsCAGCATTCATGAG	ENSP00000505434.1:n.*1734+50_*1734+62delinsCAGCATTCATGAG
ENST00000679431.1:c.*1439+50_*1439+62delinsCAGCATTCATGAG	ENSP00000506440.1:n.*1439+50_*1439+62delinsCAGCATTCATGAG
ENST00000679613.1:c.1563+50_1563+62delinsCAGCATTCATGAG	ENSP00000504971.1:n.1563+50_1563+62delinsCAGCATTCATGAG
ENST00000679715.1:c.1194+50_1194+62delinsCAGCATTCATGAG	ENSP00000506228.1:n.1194+50_1194+62delinsCAGCATTCATGAG
ENST00000679824.1:c.*2869+50_*2869+62delinsCAGCATTCATGAG	ENSP00000505516.1:n.*2869+50_*2869+62delinsCAGCATTCATGAG
ENST00000679990.1:n.1848_1860delinsCAGCATTCATGAG
ENST00000680636.1:c.1563+50_1563+62delinsCAGCATTCATGAG	ENSP00000504886.1:n.1563+50_1563+62delinsCAGCATTCATGAG
ENST00000680638.1:n.1366_1378delinsCAGCATTCATGAG
ENST00000680744.1:c.*916+50_*916+62delinsCAGCATTCATGAG	ENSP00000505243.1:n.*916+50_*916+62delinsCAGCATTCATGAG
ENST00000680764.1:c.*2967+50_*2967+62delinsCAGCATTCATGAG	ENSP00000505126.1:n.*2967+50_*2967+62delinsCAGCATTCATGAG
ENST00000681319.1:n.2349+50_2349+62delinsCAGCATTCATGAG
ENST00000681367.1:c.1563+50_1563+62delinsCAGCATTCATGAG	ENSP00000505309.1:n.1563+50_1563+62delinsCAGCATTCATGAG
ENST00000681552.1:c.1150-3036_1150-3024delinsCAGCATTCATGAG	ENSP00000505699.1:n.1150-3036_1150-3024delinsCAGCATTCATGAG
ENST00000681583.1:c.1563+50_1563+62delinsCAGCATTCATGAG	ENSP00000506340.1:n.1563+50_1563+62delinsCAGCATTCATGAG
ENST00000681585.1:c.*182+50_*182+62delinsCAGCATTCATGAG	ENSP00000506316.1:n.*182+50_*182+62delinsCAGCATTCATGAG
ENST00000681784.1:n.1691_1703delinsCAGCATTCATGAG
ENST00000681886.1:c.*806_*818delinsCAGCATTCATGAG	ENSP00000506500.1:n.*806_*818delinsCAGCATTCATGAG
ENST00000308982.11:c.1563+50_1563+62delinsCAGCATTCATGAG	ENSP00000312618.7:n.1563+50_1563+62delinsCAGCATTCATGAG
ENST00000505867.5:c.*1363+50_*1363+62delinsCAGCATTCATGAG	ENSP00000425346.1:n.*1363+50_*1363+62delinsCAGCATTCATGAG
ENST00000508971.1:c.852+50_852+62delinsCAGCATTCATGAG	ENSP00000422683.1:n.852+50_852+62delinsCAGCATTCATGAG
ENST00000511227.5:c.*1457+50_*1457+62delinsCAGCATTCATGAG	ENSP00000425226.1:n.*1457+50_*1457+62delinsCAGCATTCATGAG
ENST00000511325.1:n.594_606delinsCAGCATTCATGAG
ENST00000511526.5:n.1096+50_1096+62delinsCAGCATTCATGAG
NM_014049.4:c.1563+50_1563+62delinsCAGCATTCATGAG	NP_054768.2:n.1563+50_1563+62delinsCAGCATTCATGAG
NR_033426.1:n.1941+50_1941+62delinsCAGCATTCATGAG
XM_011512742.1:c.1194+50_1194+62delinsCAGCATTCATGAG	XP_011511044.1:n.1194+50_1194+62delinsCAGCATTCATGAG
XM_024453484.1:c.1194+50_1194+62delinsCAGCATTCATGAG	XP_024309252.1:n.1194+50_1194+62delinsCAGCATTCATGAG
XM_024453485.1:c.1194+50_1194+62delinsCAGCATTCATGAG	XP_024309253.1:n.1194+50_1194+62delinsCAGCATTCATGAG
XR_427367.3:n.1639+50_1639+62delinsCAGCATTCATGAG
NM_014049.5:c.1563+50_1563+62delinsCAGCATTCATGAG MANE Select	NP_054768.2:n.1563+50_1563+62delinsCAGCATTCATGAG
NR_033426.2:n.1811+50_1811+62delinsCAGCATTCATGAG