Canonical Allele Identifier: CA353816

Gene: ACAD9

Linked Data

• ClinVar Variation Id: 242467
• ClinVar RCV Id: RCV003556293
• dbSNP Id: rs863225058
• MyVariant Identifiers: chr3:g.128603494A>G (hg19) ; chr3:g.128884651A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128884651A>G , CM000665.2:g.128884651A>G	GRCh38
NC_000003.11:g.128603494A>G , CM000665.1:g.128603494A>G	GRCh37
NC_000003.10:g.130086184A>G	NCBI36
NG_017064.1:g.10162A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.151-2A>G MANE Select	ENSP00000312618.7:n.151-2A>G
ENST00000511325.2:n.229-2A>G
ENST00000679399.1:c.*45-2A>G	ENSP00000505434.1:n.*45-2A>G
ENST00000679431.1:c.*45-24A>G	ENSP00000506440.1:n.*45-24A>G
ENST00000679613.1:c.151-2A>G	ENSP00000504971.1:n.151-2A>G
ENST00000679715.1:c.-221A>G	ENSP00000506228.1:n.-221A>G
ENST00000679824.1:c.*1550+3128A>G	ENSP00000505516.1:n.*1550+3128A>G
ENST00000679990.1:n.390-6A>G
ENST00000680636.1:c.151-2A>G	ENSP00000504886.1:n.151-2A>G
ENST00000680744.1:c.151-2A>G	ENSP00000505243.1:n.151-2A>G
ENST00000680764.1:c.*1551-2A>G	ENSP00000505126.1:n.*1551-2A>G
ENST00000681319.1:n.229-2A>G
ENST00000681367.1:c.151-2A>G	ENSP00000505309.1:n.151-2A>G
ENST00000681552.1:c.151-2A>G	ENSP00000505699.1:n.151-2A>G
ENST00000681583.1:c.151-2A>G	ENSP00000506340.1:n.151-2A>G
ENST00000681585.1:c.151-2A>G	ENSP00000506316.1:n.151-2A>G
ENST00000681589.1:n.365-2A>G
ENST00000681784.1:n.229-2A>G
ENST00000681886.1:c.151-2A>G	ENSP00000506500.1:n.151-2A>G
ENST00000308982.11:c.151-2A>G	ENSP00000312618.7:n.151-2A>G
ENST00000505192.5:c.150+4810A>G	ENSP00000426277.1:n.150+4810A>G
ENST00000505602.1:n.517-2A>G
ENST00000505867.5:c.*44+4634A>G	ENSP00000425346.1:n.*44+4634A>G
ENST00000511227.5:c.*45-2A>G	ENSP00000425226.1:n.*45-2A>G
ENST00000512801.5:c.151-24A>G	ENSP00000427283.1:n.151-24A>G
ENST00000514336.1:c.151-2A>G	ENSP00000423758.1:n.151-2A>G
ENST00000514643.5:c.151-6A>G	ENSP00000422020.1:n.151-6A>G
ENST00000515429.1:c.*45-2A>G	ENSP00000426189.1:n.*45-2A>G
NM_014049.4:c.151-2A>G	NP_054768.2:n.151-2A>G
NR_033426.1:n.529-2A>G
XM_011512742.1:c.-219-2A>G	XP_011511044.1:n.-219-2A>G
XR_427367.1:n.223-2A>G
XM_024453484.1:c.-219-2A>G	XP_024309252.1:n.-219-2A>G
XM_024453485.1:c.-126+4810A>G	XP_024309253.1:n.-126+4810A>G
XR_427367.3:n.223-2A>G
NM_014049.5:c.151-2A>G MANE Select	NP_054768.2:n.151-2A>G
NR_033426.2:n.399-2A>G