Canonical Allele Identifier: CA2667561431

Gene: ACAD9

Linked Data

• gnomAD v4: 3-128909556-GGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909558_128909559del , CM000665.2:g.128909558_128909559del	GRCh38
NC_000003.11:g.128628401_128628402del , CM000665.1:g.128628401_128628402del	GRCh37
NC_000003.10:g.130111091_130111092del	NCBI36
NG_017064.1:g.35069_35070del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1563+137_1563+138del MANE Select	ENSP00000312618.7:n.1563+137_1563+138del
ENST00000511325.2:n.1778_1779del
ENST00000679399.1:c.*1734+137_*1734+138del	ENSP00000505434.1:n.*1734+137_*1734+138del
ENST00000679431.1:c.*1439+137_*1439+138del	ENSP00000506440.1:n.*1439+137_*1439+138del
ENST00000679613.1:c.1563+137_1563+138del	ENSP00000504971.1:n.1563+137_1563+138del
ENST00000679715.1:c.1194+137_1194+138del	ENSP00000506228.1:n.1194+137_1194+138del
ENST00000679824.1:c.*2869+137_*2869+138del	ENSP00000505516.1:n.*2869+137_*2869+138del
ENST00000679990.1:n.1935_1936del
ENST00000680636.1:c.1563+137_1563+138del	ENSP00000504886.1:n.1563+137_1563+138del
ENST00000680638.1:n.1453_1454del
ENST00000680744.1:c.*916+137_*916+138del	ENSP00000505243.1:n.*916+137_*916+138del
ENST00000680764.1:c.*2967+137_*2967+138del	ENSP00000505126.1:n.*2967+137_*2967+138del
ENST00000681319.1:n.2349+137_2349+138del
ENST00000681367.1:c.1563+137_1563+138del	ENSP00000505309.1:n.1563+137_1563+138del
ENST00000681552.1:c.1150-2949_1150-2948del	ENSP00000505699.1:n.1150-2949_1150-2948del
ENST00000681583.1:c.1563+137_1563+138del	ENSP00000506340.1:n.1563+137_1563+138del
ENST00000681585.1:c.*182+137_*182+138del	ENSP00000506316.1:n.*182+137_*182+138del
ENST00000681784.1:n.1778_1779del
ENST00000681886.1:c.*893_*894del	ENSP00000506500.1:n.*893_*894del
ENST00000308982.11:c.1563+137_1563+138del	ENSP00000312618.7:n.1563+137_1563+138del
ENST00000505867.5:c.*1363+137_*1363+138del	ENSP00000425346.1:n.*1363+137_*1363+138del
ENST00000508971.1:c.852+137_852+138del	ENSP00000422683.1:n.852+137_852+138del
ENST00000511227.5:c.*1457+137_*1457+138del	ENSP00000425226.1:n.*1457+137_*1457+138del
ENST00000511325.1:n.681_682del
ENST00000511526.5:n.1096+137_1096+138del
NM_014049.4:c.1563+137_1563+138del	NP_054768.2:n.1563+137_1563+138del
NR_033426.1:n.1941+137_1941+138del
XM_011512742.1:c.1194+137_1194+138del	XP_011511044.1:n.1194+137_1194+138del
XM_024453484.1:c.1194+137_1194+138del	XP_024309252.1:n.1194+137_1194+138del
XM_024453485.1:c.1194+137_1194+138del	XP_024309253.1:n.1194+137_1194+138del
XR_427367.3:n.1639+137_1639+138del
NM_014049.5:c.1563+137_1563+138del MANE Select	NP_054768.2:n.1563+137_1563+138del
NR_033426.2:n.1811+137_1811+138del