Canonical Allele Identifier: CA1400926971

Gene: ACAD9

Linked Data

• dbSNP Id: rs1936046925

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909488_128909490del , CM000665.2:g.128909488_128909490del	GRCh38
NC_000003.11:g.128628331_128628333del , CM000665.1:g.128628331_128628333del	GRCh37
NC_000003.10:g.130111021_130111023del	NCBI36
NG_017064.1:g.34999_35001del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1563+67_1563+69del MANE Select	ENSP00000312618.7:n.1563+67_1563+69del
ENST00000511325.2:n.1708_1710del
ENST00000679399.1:c.*1734+67_*1734+69del	ENSP00000505434.1:n.*1734+67_*1734+69del
ENST00000679431.1:c.*1439+67_*1439+69del	ENSP00000506440.1:n.*1439+67_*1439+69del
ENST00000679613.1:c.1563+67_1563+69del	ENSP00000504971.1:n.1563+67_1563+69del
ENST00000679715.1:c.1194+67_1194+69del	ENSP00000506228.1:n.1194+67_1194+69del
ENST00000679824.1:c.*2869+67_*2869+69del	ENSP00000505516.1:n.*2869+67_*2869+69del
ENST00000679990.1:n.1865_1867del
ENST00000680636.1:c.1563+67_1563+69del	ENSP00000504886.1:n.1563+67_1563+69del
ENST00000680638.1:n.1383_1385del
ENST00000680744.1:c.*916+67_*916+69del	ENSP00000505243.1:n.*916+67_*916+69del
ENST00000680764.1:c.*2967+67_*2967+69del	ENSP00000505126.1:n.*2967+67_*2967+69del
ENST00000681319.1:n.2349+67_2349+69del
ENST00000681367.1:c.1563+67_1563+69del	ENSP00000505309.1:n.1563+67_1563+69del
ENST00000681552.1:c.1150-3019_1150-3017del	ENSP00000505699.1:n.1150-3019_1150-3017del
ENST00000681583.1:c.1563+67_1563+69del	ENSP00000506340.1:n.1563+67_1563+69del
ENST00000681585.1:c.*182+67_*182+69del	ENSP00000506316.1:n.*182+67_*182+69del
ENST00000681784.1:n.1708_1710del
ENST00000681886.1:c.*823_*825del	ENSP00000506500.1:n.*823_*825del
ENST00000308982.11:c.1563+67_1563+69del	ENSP00000312618.7:n.1563+67_1563+69del
ENST00000505867.5:c.*1363+67_*1363+69del	ENSP00000425346.1:n.*1363+67_*1363+69del
ENST00000508971.1:c.852+67_852+69del	ENSP00000422683.1:n.852+67_852+69del
ENST00000511227.5:c.*1457+67_*1457+69del	ENSP00000425226.1:n.*1457+67_*1457+69del
ENST00000511325.1:n.611_613del
ENST00000511526.5:n.1096+67_1096+69del
NM_014049.4:c.1563+67_1563+69del	NP_054768.2:n.1563+67_1563+69del
NR_033426.1:n.1941+67_1941+69del
XM_011512742.1:c.1194+67_1194+69del	XP_011511044.1:n.1194+67_1194+69del
XM_024453484.1:c.1194+67_1194+69del	XP_024309252.1:n.1194+67_1194+69del
XM_024453485.1:c.1194+67_1194+69del	XP_024309253.1:n.1194+67_1194+69del
XR_427367.3:n.1639+67_1639+69del
NM_014049.5:c.1563+67_1563+69del MANE Select	NP_054768.2:n.1563+67_1563+69del
NR_033426.2:n.1811+67_1811+69del