Canonical Allele Identifier: CA898723444

Gene: ACAD9

Linked Data

• dbSNP Id: rs1308251024
• gnomAD v3: 3-128909523-AC-A
• gnomAD v4: 3-128909523-AC-A
• MyVariant Identifiers: chr3:g.128628367del (hg19) ; chr3:g.128909524del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909524del , CM000665.2:g.128909524del	GRCh38
NC_000003.11:g.128628367del , CM000665.1:g.128628367del	GRCh37
NC_000003.10:g.130111057del	NCBI36
NG_017064.1:g.35035del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1563+103del MANE Select	ENSP00000312618.7:n.1563+103del
ENST00000511325.2:n.1744del
ENST00000679399.1:c.*1734+103del	ENSP00000505434.1:n.*1734+103del
ENST00000679431.1:c.*1439+103del	ENSP00000506440.1:n.*1439+103del
ENST00000679613.1:c.1563+103del	ENSP00000504971.1:n.1563+103del
ENST00000679715.1:c.1194+103del	ENSP00000506228.1:n.1194+103del
ENST00000679824.1:c.*2869+103del	ENSP00000505516.1:n.*2869+103del
ENST00000679990.1:n.1901del
ENST00000680636.1:c.1563+103del	ENSP00000504886.1:n.1563+103del
ENST00000680638.1:n.1419del
ENST00000680744.1:c.*916+103del	ENSP00000505243.1:n.*916+103del
ENST00000680764.1:c.*2967+103del	ENSP00000505126.1:n.*2967+103del
ENST00000681319.1:n.2349+103del
ENST00000681367.1:c.1563+103del	ENSP00000505309.1:n.1563+103del
ENST00000681552.1:c.1150-2983del	ENSP00000505699.1:n.1150-2983del
ENST00000681583.1:c.1563+103del	ENSP00000506340.1:n.1563+103del
ENST00000681585.1:c.*182+103del	ENSP00000506316.1:n.*182+103del
ENST00000681784.1:n.1744del
ENST00000681886.1:c.*859del	ENSP00000506500.1:n.*859del
ENST00000308982.11:c.1563+103del	ENSP00000312618.7:n.1563+103del
ENST00000505867.5:c.*1363+103del	ENSP00000425346.1:n.*1363+103del
ENST00000508971.1:c.852+103del	ENSP00000422683.1:n.852+103del
ENST00000511227.5:c.*1457+103del	ENSP00000425226.1:n.*1457+103del
ENST00000511325.1:n.647del
ENST00000511526.5:n.1096+103del
NM_014049.4:c.1563+103del	NP_054768.2:n.1563+103del
NR_033426.1:n.1941+103del
XM_011512742.1:c.1194+103del	XP_011511044.1:n.1194+103del
XM_024453484.1:c.1194+103del	XP_024309252.1:n.1194+103del
XM_024453485.1:c.1194+103del	XP_024309253.1:n.1194+103del
XR_427367.3:n.1639+103del
NM_014049.5:c.1563+103del MANE Select	NP_054768.2:n.1563+103del
NR_033426.2:n.1811+103del