Canonical Allele Identifier: CA2667561429

Gene: ACAD9

Linked Data

• gnomAD v4: 3-128909555-TGGTGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909559_128909563del , CM000665.2:g.128909559_128909563del	GRCh38
NC_000003.11:g.128628402_128628406del , CM000665.1:g.128628402_128628406del	GRCh37
NC_000003.10:g.130111092_130111096del	NCBI36
NG_017064.1:g.35070_35074del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1563+138_1563+142del MANE Select	ENSP00000312618.7:n.1563+138_1563+142del
ENST00000511325.2:n.1779_1783del
ENST00000679399.1:c.*1734+138_*1734+142del	ENSP00000505434.1:n.*1734+138_*1734+142del
ENST00000679431.1:c.*1439+138_*1439+142del	ENSP00000506440.1:n.*1439+138_*1439+142del
ENST00000679613.1:c.1563+138_1563+142del	ENSP00000504971.1:n.1563+138_1563+142del
ENST00000679715.1:c.1194+138_1194+142del	ENSP00000506228.1:n.1194+138_1194+142del
ENST00000679824.1:c.*2869+138_*2869+142del	ENSP00000505516.1:n.*2869+138_*2869+142del
ENST00000679990.1:n.1936_1940del
ENST00000680636.1:c.1563+138_1563+142del	ENSP00000504886.1:n.1563+138_1563+142del
ENST00000680638.1:n.1454_1458del
ENST00000680744.1:c.*916+138_*916+142del	ENSP00000505243.1:n.*916+138_*916+142del
ENST00000680764.1:c.*2967+138_*2967+142del	ENSP00000505126.1:n.*2967+138_*2967+142del
ENST00000681319.1:n.2349+138_2349+142del
ENST00000681367.1:c.1563+138_1563+142del	ENSP00000505309.1:n.1563+138_1563+142del
ENST00000681552.1:c.1150-2948_1150-2944del	ENSP00000505699.1:n.1150-2948_1150-2944del
ENST00000681583.1:c.1563+138_1563+142del	ENSP00000506340.1:n.1563+138_1563+142del
ENST00000681585.1:c.*182+138_*182+142del	ENSP00000506316.1:n.*182+138_*182+142del
ENST00000681784.1:n.1779_1783del
ENST00000681886.1:c.*894_*898del	ENSP00000506500.1:n.*894_*898del
ENST00000308982.11:c.1563+138_1563+142del	ENSP00000312618.7:n.1563+138_1563+142del
ENST00000505867.5:c.*1363+138_*1363+142del	ENSP00000425346.1:n.*1363+138_*1363+142del
ENST00000508971.1:c.852+138_852+142del	ENSP00000422683.1:n.852+138_852+142del
ENST00000511227.5:c.*1457+138_*1457+142del	ENSP00000425226.1:n.*1457+138_*1457+142del
ENST00000511325.1:n.682_686del
ENST00000511526.5:n.1096+138_1096+142del
NM_014049.4:c.1563+138_1563+142del	NP_054768.2:n.1563+138_1563+142del
NR_033426.1:n.1941+138_1941+142del
XM_011512742.1:c.1194+138_1194+142del	XP_011511044.1:n.1194+138_1194+142del
XM_024453484.1:c.1194+138_1194+142del	XP_024309252.1:n.1194+138_1194+142del
XM_024453485.1:c.1194+138_1194+142del	XP_024309253.1:n.1194+138_1194+142del
XR_427367.3:n.1639+138_1639+142del
NM_014049.5:c.1563+138_1563+142del MANE Select	NP_054768.2:n.1563+138_1563+142del
NR_033426.2:n.1811+138_1811+142del