Canonical Allele Identifier: CA2667561445

Gene: ACAD9

Linked Data

• gnomAD v4: 3-128909570-G-GACTT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909571_128909574dup , CM000665.2:g.128909571_128909574dup	GRCh38
NC_000003.11:g.128628414_128628417dup , CM000665.1:g.128628414_128628417dup	GRCh37
NC_000003.10:g.130111104_130111107dup	NCBI36
NG_017064.1:g.35082_35085dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1563+150_1563+153dup MANE Select	ENSP00000312618.7:n.1563+150_1563+153dup
ENST00000511325.2:n.1791_1794dup
ENST00000679399.1:c.*1734+150_*1734+153dup	ENSP00000505434.1:n.*1734+150_*1734+153dup
ENST00000679431.1:c.*1439+150_*1439+153dup	ENSP00000506440.1:n.*1439+150_*1439+153dup
ENST00000679613.1:c.1563+150_1563+153dup	ENSP00000504971.1:n.1563+150_1563+153dup
ENST00000679715.1:c.1194+150_1194+153dup	ENSP00000506228.1:n.1194+150_1194+153dup
ENST00000679824.1:c.*2869+150_*2869+153dup	ENSP00000505516.1:n.*2869+150_*2869+153dup
ENST00000679990.1:n.1948_1951dup
ENST00000680636.1:c.1563+150_1563+153dup	ENSP00000504886.1:n.1563+150_1563+153dup
ENST00000680638.1:n.1466_1469dup
ENST00000680744.1:c.*916+150_*916+153dup	ENSP00000505243.1:n.*916+150_*916+153dup
ENST00000680764.1:c.*2967+150_*2967+153dup	ENSP00000505126.1:n.*2967+150_*2967+153dup
ENST00000681319.1:n.2349+150_2349+153dup
ENST00000681367.1:c.1563+150_1563+153dup	ENSP00000505309.1:n.1563+150_1563+153dup
ENST00000681552.1:c.1150-2936_1150-2933dup	ENSP00000505699.1:n.1150-2936_1150-2933dup
ENST00000681583.1:c.1563+150_1563+153dup	ENSP00000506340.1:n.1563+150_1563+153dup
ENST00000681585.1:c.*182+150_*182+153dup	ENSP00000506316.1:n.*182+150_*182+153dup
ENST00000681784.1:n.1791_1794dup
ENST00000681886.1:c.*906_*909dup	ENSP00000506500.1:n.*906_*909dup
ENST00000308982.11:c.1563+150_1563+153dup	ENSP00000312618.7:n.1563+150_1563+153dup
ENST00000505867.5:c.*1363+150_*1363+153dup	ENSP00000425346.1:n.*1363+150_*1363+153dup
ENST00000508971.1:c.852+150_852+153dup	ENSP00000422683.1:n.852+150_852+153dup
ENST00000511227.5:c.*1457+150_*1457+153dup	ENSP00000425226.1:n.*1457+150_*1457+153dup
ENST00000511325.1:n.694_697dup
ENST00000511526.5:n.1096+150_1096+153dup
NM_014049.4:c.1563+150_1563+153dup	NP_054768.2:n.1563+150_1563+153dup
NR_033426.1:n.1941+150_1941+153dup
XM_011512742.1:c.1194+150_1194+153dup	XP_011511044.1:n.1194+150_1194+153dup
XM_024453484.1:c.1194+150_1194+153dup	XP_024309252.1:n.1194+150_1194+153dup
XM_024453485.1:c.1194+150_1194+153dup	XP_024309253.1:n.1194+150_1194+153dup
XR_427367.3:n.1639+150_1639+153dup
NM_014049.5:c.1563+150_1563+153dup MANE Select	NP_054768.2:n.1563+150_1563+153dup
NR_033426.2:n.1811+150_1811+153dup