Canonical Allele Identifier: CA354438628

Gene: ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128628256T>G (hg19) ; chr3:g.128909413T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909413T>G , CM000665.2:g.128909413T>G	GRCh38
NC_000003.11:g.128628256T>G , CM000665.1:g.128628256T>G	GRCh37
NC_000003.10:g.130110946T>G	NCBI36
NG_017064.1:g.34924T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1555T>G MANE Select	ENSP00000312618.7:p.Phe519Val
ENST00000511325.2:n.1633T>G
ENST00000679399.1:c.*1726T>G	ENSP00000505434.1:n.*1726T>G
ENST00000679431.1:c.*1431T>G	ENSP00000506440.1:n.*1431T>G
ENST00000679613.1:c.1555T>G	ENSP00000504971.1:p.Phe519Val
ENST00000679715.1:c.1186T>G	ENSP00000506228.1:p.Phe396Val
ENST00000679824.1:c.*2861T>G	ENSP00000505516.1:n.*2861T>G
ENST00000679990.1:n.1790T>G
ENST00000680636.1:c.1555T>G	ENSP00000504886.1:p.Phe519Val
ENST00000680638.1:n.1308T>G
ENST00000680744.1:c.*908T>G	ENSP00000505243.1:n.*908T>G
ENST00000680764.1:c.*2959T>G	ENSP00000505126.1:n.*2959T>G
ENST00000681319.1:n.2341T>G
ENST00000681367.1:c.1555T>G	ENSP00000505309.1:p.Phe519Val
ENST00000681552.1:c.1150-3094T>G	ENSP00000505699.1:n.1150-3094T>G
ENST00000681583.1:c.1555T>G	ENSP00000506340.1:p.Phe519Val
ENST00000681585.1:c.*174T>G	ENSP00000506316.1:n.*174T>G
ENST00000681784.1:n.1633T>G
ENST00000681886.1:c.*748T>G	ENSP00000506500.1:n.*748T>G
ENST00000308982.11:c.1555T>G	ENSP00000312618.7:p.Phe519Val
ENST00000505867.5:c.*1355T>G	ENSP00000425346.1:n.*1355T>G
ENST00000508971.1:c.844T>G	ENSP00000422683.1:p.Phe282Val
ENST00000511227.5:c.*1449T>G	ENSP00000425226.1:n.*1449T>G
ENST00000511325.1:n.536T>G
ENST00000511526.5:n.1088T>G
NM_014049.4:c.1555T>G	NP_054768.2:p.Phe519Val
NR_033426.1:n.1933T>G
XM_011512742.1:c.1186T>G	XP_011511044.1:p.Phe396Val
XM_024453484.1:c.1186T>G	XP_024309252.1:p.Phe396Val
XM_024453485.1:c.1186T>G	XP_024309253.1:p.Phe396Val
XR_427367.3:n.1631T>G
NM_014049.5:c.1555T>G MANE Select	NP_054768.2:p.Phe519Val
NR_033426.2:n.1803T>G