Canonical Allele Identifier: CA354438635

Gene: ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128628259G>C (hg19) ; chr3:g.128909416G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909416G>C , CM000665.2:g.128909416G>C	GRCh38
NC_000003.11:g.128628259G>C , CM000665.1:g.128628259G>C	GRCh37
NC_000003.10:g.130110949G>C	NCBI36
NG_017064.1:g.34927G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1558G>C MANE Select	ENSP00000312618.7:p.Gly520Arg
ENST00000511325.2:n.1636G>C
ENST00000679399.1:c.*1729G>C	ENSP00000505434.1:n.*1729G>C
ENST00000679431.1:c.*1434G>C	ENSP00000506440.1:n.*1434G>C
ENST00000679613.1:c.1558G>C	ENSP00000504971.1:p.Gly520Arg
ENST00000679715.1:c.1189G>C	ENSP00000506228.1:p.Gly397Arg
ENST00000679824.1:c.*2864G>C	ENSP00000505516.1:n.*2864G>C
ENST00000679990.1:n.1793G>C
ENST00000680636.1:c.1558G>C	ENSP00000504886.1:p.Gly520Arg
ENST00000680638.1:n.1311G>C
ENST00000680744.1:c.*911G>C	ENSP00000505243.1:n.*911G>C
ENST00000680764.1:c.*2962G>C	ENSP00000505126.1:n.*2962G>C
ENST00000681319.1:n.2344G>C
ENST00000681367.1:c.1558G>C	ENSP00000505309.1:p.Gly520Arg
ENST00000681552.1:c.1150-3091G>C	ENSP00000505699.1:n.1150-3091G>C
ENST00000681583.1:c.1558G>C	ENSP00000506340.1:p.Gly520Arg
ENST00000681585.1:c.*177G>C	ENSP00000506316.1:n.*177G>C
ENST00000681784.1:n.1636G>C
ENST00000681886.1:c.*751G>C	ENSP00000506500.1:n.*751G>C
ENST00000308982.11:c.1558G>C	ENSP00000312618.7:p.Gly520Arg
ENST00000505867.5:c.*1358G>C	ENSP00000425346.1:n.*1358G>C
ENST00000508971.1:c.847G>C	ENSP00000422683.1:p.Gly283Arg
ENST00000511227.5:c.*1452G>C	ENSP00000425226.1:n.*1452G>C
ENST00000511325.1:n.539G>C
ENST00000511526.5:n.1091G>C
NM_014049.4:c.1558G>C	NP_054768.2:p.Gly520Arg
NR_033426.1:n.1936G>C
XM_011512742.1:c.1189G>C	XP_011511044.1:p.Gly397Arg
XM_024453484.1:c.1189G>C	XP_024309252.1:p.Gly397Arg
XM_024453485.1:c.1189G>C	XP_024309253.1:p.Gly397Arg
XR_427367.3:n.1634G>C
NM_014049.5:c.1558G>C MANE Select	NP_054768.2:p.Gly520Arg
NR_033426.2:n.1806G>C