Canonical Allele Identifier: CA435595053

Gene: ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128628237G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909394G>A , CM000665.2:g.128909394G>A	GRCh38
NC_000003.11:g.128628237G>A , CM000665.1:g.128628237G>A	GRCh37
NC_000003.10:g.130110927G>A	NCBI36
NG_017064.1:g.34905G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1536G>A MANE Select	ENSP00000312618.7:p.Val512=
ENST00000511325.2:n.1614G>A
ENST00000679399.1:c.*1707G>A	ENSP00000505434.1:n.*1707G>A
ENST00000679431.1:c.*1412G>A	ENSP00000506440.1:n.*1412G>A
ENST00000679613.1:c.1536G>A	ENSP00000504971.1:p.Val512=
ENST00000679715.1:c.1167G>A	ENSP00000506228.1:p.Val389=
ENST00000679824.1:c.*2842G>A	ENSP00000505516.1:n.*2842G>A
ENST00000679990.1:n.1771G>A
ENST00000680636.1:c.1536G>A	ENSP00000504886.1:p.Val512=
ENST00000680638.1:n.1289G>A
ENST00000680744.1:c.*889G>A	ENSP00000505243.1:n.*889G>A
ENST00000680764.1:c.*2940G>A	ENSP00000505126.1:n.*2940G>A
ENST00000681319.1:n.2322G>A
ENST00000681367.1:c.1536G>A	ENSP00000505309.1:p.Val512=
ENST00000681552.1:c.1150-3113G>A	ENSP00000505699.1:n.1150-3113G>A
ENST00000681583.1:c.1536G>A	ENSP00000506340.1:p.Val512=
ENST00000681585.1:c.*155G>A	ENSP00000506316.1:n.*155G>A
ENST00000681784.1:n.1614G>A
ENST00000681886.1:c.*729G>A	ENSP00000506500.1:n.*729G>A
ENST00000308982.11:c.1536G>A	ENSP00000312618.7:p.Val512=
ENST00000505867.5:c.*1336G>A	ENSP00000425346.1:n.*1336G>A
ENST00000508971.1:c.825G>A	ENSP00000422683.1:p.Val275=
ENST00000511227.5:c.*1430G>A	ENSP00000425226.1:n.*1430G>A
ENST00000511325.1:n.517G>A
ENST00000511526.5:n.1069G>A
NM_014049.4:c.1536G>A	NP_054768.2:p.Val512=
NR_033426.1:n.1914G>A
XM_011512742.1:c.1167G>A	XP_011511044.1:p.Val389=
XM_024453484.1:c.1167G>A	XP_024309252.1:p.Val389=
XM_024453485.1:c.1167G>A	XP_024309253.1:p.Val389=
XR_427367.3:n.1612G>A
NM_014049.5:c.1536G>A MANE Select	NP_054768.2:p.Val512=
NR_033426.2:n.1784G>A