Canonical Allele Identifier: CA82533032

Gene: ACAD9

Linked Data

• dbSNP Id: rs894710681
• gnomAD v3: 3-128904272-GGCTT-G
• gnomAD v4: 3-128904272-GGCTT-G
• MyVariant Identifiers: chr3:g.128623116_128623119del (hg19) ; chr3:g.128904273_128904276del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128904277_128904280del , CM000665.2:g.128904277_128904280del	GRCh38
NC_000003.11:g.128623120_128623123del , CM000665.1:g.128623120_128623123del	GRCh37
NC_000003.10:g.130105810_130105813del	NCBI36
NG_017064.1:g.29788_29791del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1030-109_1030-106del MANE Select	ENSP00000312618.7:n.1030-109_1030-106del
ENST00000511325.2:n.1108-109_1108-106del
ENST00000679399.1:c.*924-109_*924-106del	ENSP00000505434.1:n.*924-109_*924-106del
ENST00000679431.1:c.*906-109_*906-106del	ENSP00000506440.1:n.*906-109_*906-106del
ENST00000679613.1:c.1030-109_1030-106del	ENSP00000504971.1:n.1030-109_1030-106del
ENST00000679715.1:c.661-109_661-106del	ENSP00000506228.1:n.661-109_661-106del
ENST00000679824.1:c.*2336-109_*2336-106del	ENSP00000505516.1:n.*2336-109_*2336-106del
ENST00000679990.1:n.1265-109_1265-106del
ENST00000680636.1:c.1030-109_1030-106del	ENSP00000504886.1:n.1030-109_1030-106del
ENST00000680744.1:c.*383-109_*383-106del	ENSP00000505243.1:n.*383-109_*383-106del
ENST00000680764.1:c.*2434-109_*2434-106del	ENSP00000505126.1:n.*2434-109_*2434-106del
ENST00000681319.1:n.1108-109_1108-106del
ENST00000681367.1:c.1030-109_1030-106del	ENSP00000505309.1:n.1030-109_1030-106del
ENST00000681552.1:c.1030-109_1030-106del	ENSP00000505699.1:n.1030-109_1030-106del
ENST00000681583.1:c.1030-109_1030-106del	ENSP00000506340.1:n.1030-109_1030-106del
ENST00000681585.1:c.1030-109_1030-106del	ENSP00000506316.1:n.1030-109_1030-106del
ENST00000681589.1:n.1244-109_1244-106del
ENST00000681784.1:n.1108-109_1108-106del
ENST00000681886.1:c.*223-109_*223-106del	ENSP00000506500.1:n.*223-109_*223-106del
ENST00000308982.11:c.1030-109_1030-106del	ENSP00000312618.7:n.1030-109_1030-106del
ENST00000505192.5:c.*726-109_*726-106del	ENSP00000426277.1:n.*726-109_*726-106del
ENST00000505867.5:c.*830-109_*830-106del	ENSP00000425346.1:n.*830-109_*830-106del
ENST00000508971.1:c.319-109_319-106del	ENSP00000422683.1:n.319-109_319-106del
ENST00000511227.5:c.*924-109_*924-106del	ENSP00000425226.1:n.*924-109_*924-106del
ENST00000511526.5:n.535-81_535-78del
NM_014049.4:c.1030-109_1030-106del	NP_054768.2:n.1030-109_1030-106del
NR_033426.1:n.1408-109_1408-106del
XM_011512742.1:c.661-109_661-106del	XP_011511044.1:n.661-109_661-106del
XR_427367.1:n.1106-109_1106-106del
XM_024453484.1:c.661-109_661-106del	XP_024309252.1:n.661-109_661-106del
XM_024453485.1:c.661-109_661-106del	XP_024309253.1:n.661-109_661-106del
XR_427367.3:n.1106-109_1106-106del
NM_014049.5:c.1030-109_1030-106del MANE Select	NP_054768.2:n.1030-109_1030-106del
NR_033426.2:n.1278-109_1278-106del