Canonical Allele Identifier: CA2604295012

Gene: ACAD9

Linked Data

• gnomAD v3: 3-128909567-GCTGA-G
• gnomAD v4: 3-128909567-GCTGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909570_128909573del , CM000665.2:g.128909570_128909573del	GRCh38
NC_000003.11:g.128628413_128628416del , CM000665.1:g.128628413_128628416del	GRCh37
NC_000003.10:g.130111103_130111106del	NCBI36
NG_017064.1:g.35081_35084del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1563+149_1563+152del MANE Select	ENSP00000312618.7:n.1563+149_1563+152del
ENST00000511325.2:n.1790_1793del
ENST00000679399.1:c.*1734+149_*1734+152del	ENSP00000505434.1:n.*1734+149_*1734+152del
ENST00000679431.1:c.*1439+149_*1439+152del	ENSP00000506440.1:n.*1439+149_*1439+152del
ENST00000679613.1:c.1563+149_1563+152del	ENSP00000504971.1:n.1563+149_1563+152del
ENST00000679715.1:c.1194+149_1194+152del	ENSP00000506228.1:n.1194+149_1194+152del
ENST00000679824.1:c.*2869+149_*2869+152del	ENSP00000505516.1:n.*2869+149_*2869+152del
ENST00000679990.1:n.1947_1950del
ENST00000680636.1:c.1563+149_1563+152del	ENSP00000504886.1:n.1563+149_1563+152del
ENST00000680638.1:n.1465_1468del
ENST00000680744.1:c.*916+149_*916+152del	ENSP00000505243.1:n.*916+149_*916+152del
ENST00000680764.1:c.*2967+149_*2967+152del	ENSP00000505126.1:n.*2967+149_*2967+152del
ENST00000681319.1:n.2349+149_2349+152del
ENST00000681367.1:c.1563+149_1563+152del	ENSP00000505309.1:n.1563+149_1563+152del
ENST00000681552.1:c.1150-2937_1150-2934del	ENSP00000505699.1:n.1150-2937_1150-2934del
ENST00000681583.1:c.1563+149_1563+152del	ENSP00000506340.1:n.1563+149_1563+152del
ENST00000681585.1:c.*182+149_*182+152del	ENSP00000506316.1:n.*182+149_*182+152del
ENST00000681784.1:n.1790_1793del
ENST00000681886.1:c.*905_*908del	ENSP00000506500.1:n.*905_*908del
ENST00000308982.11:c.1563+149_1563+152del	ENSP00000312618.7:n.1563+149_1563+152del
ENST00000505867.5:c.*1363+149_*1363+152del	ENSP00000425346.1:n.*1363+149_*1363+152del
ENST00000508971.1:c.852+149_852+152del	ENSP00000422683.1:n.852+149_852+152del
ENST00000511227.5:c.*1457+149_*1457+152del	ENSP00000425226.1:n.*1457+149_*1457+152del
ENST00000511325.1:n.693_696del
ENST00000511526.5:n.1096+149_1096+152del
NM_014049.4:c.1563+149_1563+152del	NP_054768.2:n.1563+149_1563+152del
NR_033426.1:n.1941+149_1941+152del
XM_011512742.1:c.1194+149_1194+152del	XP_011511044.1:n.1194+149_1194+152del
XM_024453484.1:c.1194+149_1194+152del	XP_024309252.1:n.1194+149_1194+152del
XM_024453485.1:c.1194+149_1194+152del	XP_024309253.1:n.1194+149_1194+152del
XR_427367.3:n.1639+149_1639+152del
NM_014049.5:c.1563+149_1563+152del MANE Select	NP_054768.2:n.1563+149_1563+152del
NR_033426.2:n.1811+149_1811+152del