Canonical Allele Identifier: CA2667561401

Gene: ACAD9

Linked Data

• gnomAD v4: 3-128909529-A-ATGT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909532_128909534dup , CM000665.2:g.128909532_128909534dup	GRCh38
NC_000003.11:g.128628375_128628377dup , CM000665.1:g.128628375_128628377dup	GRCh37
NC_000003.10:g.130111065_130111067dup	NCBI36
NG_017064.1:g.35043_35045dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1563+111_1563+113dup MANE Select	ENSP00000312618.7:n.1563+111_1563+113dup
ENST00000511325.2:n.1752_1754dup
ENST00000679399.1:c.*1734+111_*1734+113dup	ENSP00000505434.1:n.*1734+111_*1734+113dup
ENST00000679431.1:c.*1439+111_*1439+113dup	ENSP00000506440.1:n.*1439+111_*1439+113dup
ENST00000679613.1:c.1563+111_1563+113dup	ENSP00000504971.1:n.1563+111_1563+113dup
ENST00000679715.1:c.1194+111_1194+113dup	ENSP00000506228.1:n.1194+111_1194+113dup
ENST00000679824.1:c.*2869+111_*2869+113dup	ENSP00000505516.1:n.*2869+111_*2869+113dup
ENST00000679990.1:n.1909_1911dup
ENST00000680636.1:c.1563+111_1563+113dup	ENSP00000504886.1:n.1563+111_1563+113dup
ENST00000680638.1:n.1427_1429dup
ENST00000680744.1:c.*916+111_*916+113dup	ENSP00000505243.1:n.*916+111_*916+113dup
ENST00000680764.1:c.*2967+111_*2967+113dup	ENSP00000505126.1:n.*2967+111_*2967+113dup
ENST00000681319.1:n.2349+111_2349+113dup
ENST00000681367.1:c.1563+111_1563+113dup	ENSP00000505309.1:n.1563+111_1563+113dup
ENST00000681552.1:c.1150-2975_1150-2973dup	ENSP00000505699.1:n.1150-2975_1150-2973dup
ENST00000681583.1:c.1563+111_1563+113dup	ENSP00000506340.1:n.1563+111_1563+113dup
ENST00000681585.1:c.*182+111_*182+113dup	ENSP00000506316.1:n.*182+111_*182+113dup
ENST00000681784.1:n.1752_1754dup
ENST00000681886.1:c.*867_*869dup	ENSP00000506500.1:n.*867_*869dup
ENST00000308982.11:c.1563+111_1563+113dup	ENSP00000312618.7:n.1563+111_1563+113dup
ENST00000505867.5:c.*1363+111_*1363+113dup	ENSP00000425346.1:n.*1363+111_*1363+113dup
ENST00000508971.1:c.852+111_852+113dup	ENSP00000422683.1:n.852+111_852+113dup
ENST00000511227.5:c.*1457+111_*1457+113dup	ENSP00000425226.1:n.*1457+111_*1457+113dup
ENST00000511325.1:n.655_657dup
ENST00000511526.5:n.1096+111_1096+113dup
NM_014049.4:c.1563+111_1563+113dup	NP_054768.2:n.1563+111_1563+113dup
NR_033426.1:n.1941+111_1941+113dup
XM_011512742.1:c.1194+111_1194+113dup	XP_011511044.1:n.1194+111_1194+113dup
XM_024453484.1:c.1194+111_1194+113dup	XP_024309252.1:n.1194+111_1194+113dup
XM_024453485.1:c.1194+111_1194+113dup	XP_024309253.1:n.1194+111_1194+113dup
XR_427367.3:n.1639+111_1639+113dup
NM_014049.5:c.1563+111_1563+113dup MANE Select	NP_054768.2:n.1563+111_1563+113dup
NR_033426.2:n.1811+111_1811+113dup