Canonical Allele Identifier: CA898723463

Gene: ACAD9

Linked Data

• dbSNP Id: rs1161138348
• gnomAD v3: 3-128909572-CTT-C
• gnomAD v4: 3-128909572-CTT-C
• MyVariant Identifiers: chr3:g.128628416_128628417del (hg19) ; chr3:g.128909573_128909574del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909574_128909575del , CM000665.2:g.128909574_128909575del	GRCh38
NC_000003.11:g.128628417_128628418del , CM000665.1:g.128628417_128628418del	GRCh37
NC_000003.10:g.130111107_130111108del	NCBI36
NG_017064.1:g.35085_35086del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1563+153_1563+154del MANE Select	ENSP00000312618.7:n.1563+153_1563+154del
ENST00000511325.2:n.1794_1795del
ENST00000679399.1:c.*1734+153_*1734+154del	ENSP00000505434.1:n.*1734+153_*1734+154del
ENST00000679431.1:c.*1439+153_*1439+154del	ENSP00000506440.1:n.*1439+153_*1439+154del
ENST00000679613.1:c.1563+153_1563+154del	ENSP00000504971.1:n.1563+153_1563+154del
ENST00000679715.1:c.1194+153_1194+154del	ENSP00000506228.1:n.1194+153_1194+154del
ENST00000679824.1:c.*2869+153_*2869+154del	ENSP00000505516.1:n.*2869+153_*2869+154del
ENST00000679990.1:n.1951_1952del
ENST00000680636.1:c.1563+153_1563+154del	ENSP00000504886.1:n.1563+153_1563+154del
ENST00000680638.1:n.1469_1470del
ENST00000680744.1:c.*916+153_*916+154del	ENSP00000505243.1:n.*916+153_*916+154del
ENST00000680764.1:c.*2967+153_*2967+154del	ENSP00000505126.1:n.*2967+153_*2967+154del
ENST00000681319.1:n.2349+153_2349+154del
ENST00000681367.1:c.1563+153_1563+154del	ENSP00000505309.1:n.1563+153_1563+154del
ENST00000681552.1:c.1150-2933_1150-2932del	ENSP00000505699.1:n.1150-2933_1150-2932del
ENST00000681583.1:c.1563+153_1563+154del	ENSP00000506340.1:n.1563+153_1563+154del
ENST00000681585.1:c.*182+153_*182+154del	ENSP00000506316.1:n.*182+153_*182+154del
ENST00000681784.1:n.1794_1795del
ENST00000681886.1:c.*909_*910del	ENSP00000506500.1:n.*909_*910del
ENST00000308982.11:c.1563+153_1563+154del	ENSP00000312618.7:n.1563+153_1563+154del
ENST00000505867.5:c.*1363+153_*1363+154del	ENSP00000425346.1:n.*1363+153_*1363+154del
ENST00000508971.1:c.852+153_852+154del	ENSP00000422683.1:n.852+153_852+154del
ENST00000511227.5:c.*1457+153_*1457+154del	ENSP00000425226.1:n.*1457+153_*1457+154del
ENST00000511325.1:n.697_698del
ENST00000511526.5:n.1096+153_1096+154del
NM_014049.4:c.1563+153_1563+154del	NP_054768.2:n.1563+153_1563+154del
NR_033426.1:n.1941+153_1941+154del
XM_011512742.1:c.1194+153_1194+154del	XP_011511044.1:n.1194+153_1194+154del
XM_024453484.1:c.1194+153_1194+154del	XP_024309252.1:n.1194+153_1194+154del
XM_024453485.1:c.1194+153_1194+154del	XP_024309253.1:n.1194+153_1194+154del
XR_427367.3:n.1639+153_1639+154del
NM_014049.5:c.1563+153_1563+154del MANE Select	NP_054768.2:n.1563+153_1563+154del
NR_033426.2:n.1811+153_1811+154del