Canonical Allele Identifier: CA354438422

Gene: ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909076G>T , CM000665.2:g.128909076G>T	GRCh38
NC_000003.11:g.128627919G>T , CM000665.1:g.128627919G>T	GRCh37
NC_000003.10:g.130110609G>T	NCBI36
NG_017064.1:g.34587G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1462G>T MANE Select	ENSP00000312618.7:p.Gly488Ter
ENST00000511325.2:n.1540G>T
ENST00000679399.1:c.*1633G>T	ENSP00000505434.1:n.*1633G>T
ENST00000679431.1:c.*1338G>T	ENSP00000506440.1:n.*1338G>T
ENST00000679613.1:c.1462G>T	ENSP00000504971.1:p.Gly488Ter
ENST00000679715.1:c.1093G>T	ENSP00000506228.1:p.Gly365Ter
ENST00000679824.1:c.*2768G>T	ENSP00000505516.1:n.*2768G>T
ENST00000679990.1:n.1697G>T
ENST00000680636.1:c.1462G>T	ENSP00000504886.1:p.Gly488Ter
ENST00000680638.1:n.1215G>T
ENST00000680744.1:c.*815G>T	ENSP00000505243.1:n.*815G>T
ENST00000680764.1:c.*2866G>T	ENSP00000505126.1:n.*2866G>T
ENST00000681319.1:n.2248G>T
ENST00000681367.1:c.1462G>T	ENSP00000505309.1:p.Gly488Ter
ENST00000681552.1:c.1150-3431G>T	ENSP00000505699.1:n.1150-3431G>T
ENST00000681583.1:c.1462G>T	ENSP00000506340.1:p.Gly488Ter
ENST00000681585.1:c.*81G>T	ENSP00000506316.1:n.*81G>T
ENST00000681784.1:n.1540G>T
ENST00000681886.1:c.*655G>T	ENSP00000506500.1:n.*655G>T
ENST00000308982.11:c.1462G>T	ENSP00000312618.7:p.Gly488Ter
ENST00000505867.5:c.*1262G>T	ENSP00000425346.1:n.*1262G>T
ENST00000508971.1:c.751G>T	ENSP00000422683.1:p.Gly251Ter
ENST00000511227.5:c.*1356G>T	ENSP00000425226.1:n.*1356G>T
ENST00000511325.1:n.443G>T
ENST00000511526.5:n.995G>T
NM_014049.4:c.1462G>T	NP_054768.2:p.Gly488Ter
NR_033426.1:n.1840G>T
XM_011512742.1:c.1093G>T	XP_011511044.1:p.Gly365Ter
XM_024453484.1:c.1093G>T	XP_024309252.1:p.Gly365Ter
XM_024453485.1:c.1093G>T	XP_024309253.1:p.Gly365Ter
XR_427367.3:n.1538G>T
NM_014049.5:c.1462G>T MANE Select	NP_054768.2:p.Gly488Ter
NR_033426.2:n.1710G>T