Canonical Allele Identifier: CA2601599

Gene: ACAD9

Linked Data

• dbSNP Id: rs750522467
• ExAC: 3:128628314 CAGCAT / C
• gnomAD v2: 3-128628314-CAGCAT-C
• gnomAD v4: 3-128909471-CAGCAT-C
• MyVariant Identifiers: chr3:g.128628315_128628319del (hg19) ; chr3:g.128909472_128909476del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909472_128909476del , CM000665.2:g.128909472_128909476del	GRCh38
NC_000003.11:g.128628315_128628319del , CM000665.1:g.128628315_128628319del	GRCh37
NC_000003.10:g.130111005_130111009del	NCBI36
NG_017064.1:g.34983_34987del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1563+51_1563+55del MANE Select	ENSP00000312618.7:n.1563+51_1563+55del
ENST00000511325.2:n.1692_1696del
ENST00000679399.1:c.*1734+51_*1734+55del	ENSP00000505434.1:n.*1734+51_*1734+55del
ENST00000679431.1:c.*1439+51_*1439+55del	ENSP00000506440.1:n.*1439+51_*1439+55del
ENST00000679613.1:c.1563+51_1563+55del	ENSP00000504971.1:n.1563+51_1563+55del
ENST00000679715.1:c.1194+51_1194+55del	ENSP00000506228.1:n.1194+51_1194+55del
ENST00000679824.1:c.*2869+51_*2869+55del	ENSP00000505516.1:n.*2869+51_*2869+55del
ENST00000679990.1:n.1849_1853del
ENST00000680636.1:c.1563+51_1563+55del	ENSP00000504886.1:n.1563+51_1563+55del
ENST00000680638.1:n.1367_1371del
ENST00000680744.1:c.*916+51_*916+55del	ENSP00000505243.1:n.*916+51_*916+55del
ENST00000680764.1:c.*2967+51_*2967+55del	ENSP00000505126.1:n.*2967+51_*2967+55del
ENST00000681319.1:n.2349+51_2349+55del
ENST00000681367.1:c.1563+51_1563+55del	ENSP00000505309.1:n.1563+51_1563+55del
ENST00000681552.1:c.1150-3035_1150-3031del	ENSP00000505699.1:n.1150-3035_1150-3031del
ENST00000681583.1:c.1563+51_1563+55del	ENSP00000506340.1:n.1563+51_1563+55del
ENST00000681585.1:c.*182+51_*182+55del	ENSP00000506316.1:n.*182+51_*182+55del
ENST00000681784.1:n.1692_1696del
ENST00000681886.1:c.*807_*811del	ENSP00000506500.1:n.*807_*811del
ENST00000308982.11:c.1563+51_1563+55del	ENSP00000312618.7:n.1563+51_1563+55del
ENST00000505867.5:c.*1363+51_*1363+55del	ENSP00000425346.1:n.*1363+51_*1363+55del
ENST00000508971.1:c.852+51_852+55del	ENSP00000422683.1:n.852+51_852+55del
ENST00000511227.5:c.*1457+51_*1457+55del	ENSP00000425226.1:n.*1457+51_*1457+55del
ENST00000511325.1:n.595_599del
ENST00000511526.5:n.1096+51_1096+55del
NM_014049.4:c.1563+51_1563+55del	NP_054768.2:n.1563+51_1563+55del
NR_033426.1:n.1941+51_1941+55del
XM_011512742.1:c.1194+51_1194+55del	XP_011511044.1:n.1194+51_1194+55del
XM_024453484.1:c.1194+51_1194+55del	XP_024309252.1:n.1194+51_1194+55del
XM_024453485.1:c.1194+51_1194+55del	XP_024309253.1:n.1194+51_1194+55del
XR_427367.3:n.1639+51_1639+55del
NM_014049.5:c.1563+51_1563+55del MANE Select	NP_054768.2:n.1563+51_1563+55del
NR_033426.2:n.1811+51_1811+55del