Canonical Allele Identifier: CA354438519

Gene: ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128628203T>G (hg19) ; chr3:g.128909360T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909360T>G , CM000665.2:g.128909360T>G	GRCh38
NC_000003.11:g.128628203T>G , CM000665.1:g.128628203T>G	GRCh37
NC_000003.10:g.130110893T>G	NCBI36
NG_017064.1:g.34871T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1502T>G MANE Select	ENSP00000312618.7:p.Phe501Cys
ENST00000511325.2:n.1580T>G
ENST00000679399.1:c.*1673T>G	ENSP00000505434.1:n.*1673T>G
ENST00000679431.1:c.*1378T>G	ENSP00000506440.1:n.*1378T>G
ENST00000679613.1:c.1502T>G	ENSP00000504971.1:p.Phe501Cys
ENST00000679715.1:c.1133T>G	ENSP00000506228.1:p.Phe378Cys
ENST00000679824.1:c.*2808T>G	ENSP00000505516.1:n.*2808T>G
ENST00000679990.1:n.1737T>G
ENST00000680636.1:c.1502T>G	ENSP00000504886.1:p.Phe501Cys
ENST00000680638.1:n.1255T>G
ENST00000680744.1:c.*855T>G	ENSP00000505243.1:n.*855T>G
ENST00000680764.1:c.*2906T>G	ENSP00000505126.1:n.*2906T>G
ENST00000681319.1:n.2288T>G
ENST00000681367.1:c.1502T>G	ENSP00000505309.1:p.Phe501Cys
ENST00000681552.1:c.1150-3147T>G	ENSP00000505699.1:n.1150-3147T>G
ENST00000681583.1:c.1502T>G	ENSP00000506340.1:p.Phe501Cys
ENST00000681585.1:c.*121T>G	ENSP00000506316.1:n.*121T>G
ENST00000681784.1:n.1580T>G
ENST00000681886.1:c.*695T>G	ENSP00000506500.1:n.*695T>G
ENST00000308982.11:c.1502T>G	ENSP00000312618.7:p.Phe501Cys
ENST00000505867.5:c.*1302T>G	ENSP00000425346.1:n.*1302T>G
ENST00000508971.1:c.791T>G	ENSP00000422683.1:p.Phe264Cys
ENST00000511227.5:c.*1396T>G	ENSP00000425226.1:n.*1396T>G
ENST00000511325.1:n.483T>G
ENST00000511526.5:n.1035T>G
NM_014049.4:c.1502T>G	NP_054768.2:p.Phe501Cys
NR_033426.1:n.1880T>G
XM_011512742.1:c.1133T>G	XP_011511044.1:p.Phe378Cys
XM_024453484.1:c.1133T>G	XP_024309252.1:p.Phe378Cys
XM_024453485.1:c.1133T>G	XP_024309253.1:p.Phe378Cys
XR_427367.3:n.1578T>G
NM_014049.5:c.1502T>G MANE Select	NP_054768.2:p.Phe501Cys
NR_033426.2:n.1750T>G