Canonical Allele Identifier: CA354438511

Gene: ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128628200A>G (hg19) ; chr3:g.128909357A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909357A>G , CM000665.2:g.128909357A>G	GRCh38
NC_000003.11:g.128628200A>G , CM000665.1:g.128628200A>G	GRCh37
NC_000003.10:g.130110890A>G	NCBI36
NG_017064.1:g.34868A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1499A>G MANE Select	ENSP00000312618.7:p.Lys500Arg
ENST00000511325.2:n.1577A>G
ENST00000679399.1:c.*1670A>G	ENSP00000505434.1:n.*1670A>G
ENST00000679431.1:c.*1375A>G	ENSP00000506440.1:n.*1375A>G
ENST00000679613.1:c.1499A>G	ENSP00000504971.1:p.Lys500Arg
ENST00000679715.1:c.1130A>G	ENSP00000506228.1:p.Lys377Arg
ENST00000679824.1:c.*2805A>G	ENSP00000505516.1:n.*2805A>G
ENST00000679990.1:n.1734A>G
ENST00000680636.1:c.1499A>G	ENSP00000504886.1:p.Lys500Arg
ENST00000680638.1:n.1252A>G
ENST00000680744.1:c.*852A>G	ENSP00000505243.1:n.*852A>G
ENST00000680764.1:c.*2903A>G	ENSP00000505126.1:n.*2903A>G
ENST00000681319.1:n.2285A>G
ENST00000681367.1:c.1499A>G	ENSP00000505309.1:p.Lys500Arg
ENST00000681552.1:c.1150-3150A>G	ENSP00000505699.1:n.1150-3150A>G
ENST00000681583.1:c.1499A>G	ENSP00000506340.1:p.Lys500Arg
ENST00000681585.1:c.*118A>G	ENSP00000506316.1:n.*118A>G
ENST00000681784.1:n.1577A>G
ENST00000681886.1:c.*692A>G	ENSP00000506500.1:n.*692A>G
ENST00000308982.11:c.1499A>G	ENSP00000312618.7:p.Lys500Arg
ENST00000505867.5:c.*1299A>G	ENSP00000425346.1:n.*1299A>G
ENST00000508971.1:c.788A>G	ENSP00000422683.1:p.Lys263Arg
ENST00000511227.5:c.*1393A>G	ENSP00000425226.1:n.*1393A>G
ENST00000511325.1:n.480A>G
ENST00000511526.5:n.1032A>G
NM_014049.4:c.1499A>G	NP_054768.2:p.Lys500Arg
NR_033426.1:n.1877A>G
XM_011512742.1:c.1130A>G	XP_011511044.1:p.Lys377Arg
XM_024453484.1:c.1130A>G	XP_024309252.1:p.Lys377Arg
XM_024453485.1:c.1130A>G	XP_024309253.1:p.Lys377Arg
XR_427367.3:n.1575A>G
NM_014049.5:c.1499A>G MANE Select	NP_054768.2:p.Lys500Arg
NR_033426.2:n.1747A>G