Canonical Allele Identifier: CA1400926983

Gene: ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909523_128909524delinsAC , CM000665.2:g.128909523_128909524delinsAC	GRCh38
NC_000003.11:g.128628366_128628367delinsAC , CM000665.1:g.128628366_128628367delinsAC	GRCh37
NC_000003.10:g.130111056_130111057delinsAC	NCBI36
NG_017064.1:g.35034_35035delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1563+102_1563+103delinsAC MANE Select	ENSP00000312618.7:n.1563+102_1563+103delinsAC
ENST00000511325.2:n.1743_1744delinsAC
ENST00000679399.1:c.*1734+102_*1734+103delinsAC	ENSP00000505434.1:n.*1734+102_*1734+103delinsAC
ENST00000679431.1:c.*1439+102_*1439+103delinsAC	ENSP00000506440.1:n.*1439+102_*1439+103delinsAC
ENST00000679613.1:c.1563+102_1563+103delinsAC	ENSP00000504971.1:n.1563+102_1563+103delinsAC
ENST00000679715.1:c.1194+102_1194+103delinsAC	ENSP00000506228.1:n.1194+102_1194+103delinsAC
ENST00000679824.1:c.*2869+102_*2869+103delinsAC	ENSP00000505516.1:n.*2869+102_*2869+103delinsAC
ENST00000679990.1:n.1900_1901delinsAC
ENST00000680636.1:c.1563+102_1563+103delinsAC	ENSP00000504886.1:n.1563+102_1563+103delinsAC
ENST00000680638.1:n.1418_1419delinsAC
ENST00000680744.1:c.*916+102_*916+103delinsAC	ENSP00000505243.1:n.*916+102_*916+103delinsAC
ENST00000680764.1:c.*2967+102_*2967+103delinsAC	ENSP00000505126.1:n.*2967+102_*2967+103delinsAC
ENST00000681319.1:n.2349+102_2349+103delinsAC
ENST00000681367.1:c.1563+102_1563+103delinsAC	ENSP00000505309.1:n.1563+102_1563+103delinsAC
ENST00000681552.1:c.1150-2984_1150-2983delinsAC	ENSP00000505699.1:n.1150-2984_1150-2983delinsAC
ENST00000681583.1:c.1563+102_1563+103delinsAC	ENSP00000506340.1:n.1563+102_1563+103delinsAC
ENST00000681585.1:c.*182+102_*182+103delinsAC	ENSP00000506316.1:n.*182+102_*182+103delinsAC
ENST00000681784.1:n.1743_1744delinsAC
ENST00000681886.1:c.*858_*859delinsAC	ENSP00000506500.1:n.*858_*859delinsAC
ENST00000308982.11:c.1563+102_1563+103delinsAC	ENSP00000312618.7:n.1563+102_1563+103delinsAC
ENST00000505867.5:c.*1363+102_*1363+103delinsAC	ENSP00000425346.1:n.*1363+102_*1363+103delinsAC
ENST00000508971.1:c.852+102_852+103delinsAC	ENSP00000422683.1:n.852+102_852+103delinsAC
ENST00000511227.5:c.*1457+102_*1457+103delinsAC	ENSP00000425226.1:n.*1457+102_*1457+103delinsAC
ENST00000511325.1:n.646_647delinsAC
ENST00000511526.5:n.1096+102_1096+103delinsAC
NM_014049.4:c.1563+102_1563+103delinsAC	NP_054768.2:n.1563+102_1563+103delinsAC
NR_033426.1:n.1941+102_1941+103delinsAC
XM_011512742.1:c.1194+102_1194+103delinsAC	XP_011511044.1:n.1194+102_1194+103delinsAC
XM_024453484.1:c.1194+102_1194+103delinsAC	XP_024309252.1:n.1194+102_1194+103delinsAC
XM_024453485.1:c.1194+102_1194+103delinsAC	XP_024309253.1:n.1194+102_1194+103delinsAC
XR_427367.3:n.1639+102_1639+103delinsAC
NM_014049.5:c.1563+102_1563+103delinsAC MANE Select	NP_054768.2:n.1563+102_1563+103delinsAC
NR_033426.2:n.1811+102_1811+103delinsAC