Canonical Allele Identifier: CA1400924342
Gene: ACAD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128904091A= , CM000665.2:g.128904091A= GRCh38
NC_000003.11:g.128622934A= , CM000665.1:g.128622934A= GRCh37
NC_000003.10:g.130105624A= NCBI36
NG_017064.1:g.29602A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308982.12:c.988A= MANE Select ENSP00000312618.7:p.Lys330=
ENST00000511325.2:n.1066A=
ENST00000679399.1:c.*882A= ENSP00000505434.1:n.*882A=
ENST00000679431.1:c.*864A= ENSP00000506440.1:n.*864A=
ENST00000679613.1:c.988A= ENSP00000504971.1:p.Lys330=
ENST00000679715.1:c.619A= ENSP00000506228.1:p.Lys207=
ENST00000679824.1:c.*2294A= ENSP00000505516.1:n.*2294A=
ENST00000679990.1:n.1223A=
ENST00000680636.1:c.988A= ENSP00000504886.1:p.Lys330=
ENST00000680744.1:c.*341A= ENSP00000505243.1:n.*341A=
ENST00000680764.1:c.*2392A= ENSP00000505126.1:n.*2392A=
ENST00000681319.1:n.1066A=
ENST00000681367.1:c.988A= ENSP00000505309.1:p.Lys330=
ENST00000681552.1:c.988A= ENSP00000505699.1:p.Lys330=
ENST00000681583.1:c.988A= ENSP00000506340.1:p.Lys330=
ENST00000681585.1:c.988A= ENSP00000506316.1:p.Lys330=
ENST00000681589.1:n.1202A=
ENST00000681784.1:n.1066A=
ENST00000681886.1:c.*181A= ENSP00000506500.1:n.*181A=
ENST00000308982.11:c.988A= ENSP00000312618.7:p.Lys330=
ENST00000505192.5:c.*684A= ENSP00000426277.1:n.*684A=
ENST00000505867.5:c.*788A= ENSP00000425346.1:n.*788A=
ENST00000508971.1:c.277A= ENSP00000422683.1:p.Lys93=
ENST00000511227.5:c.*882A= ENSP00000425226.1:n.*882A=
ENST00000511526.5:n.493A=
NM_014049.4:c.988A= NP_054768.2:p.Lys330=
NR_033426.1:n.1366A=
XM_011512742.1:c.619A= XP_011511044.1:p.Lys207=
XR_427367.1:n.1064A=
XM_024453484.1:c.619A= XP_024309252.1:p.Lys207=
XM_024453485.1:c.619A= XP_024309253.1:p.Lys207=
XR_427367.3:n.1064A=
NM_014049.5:c.988A= MANE Select NP_054768.2:p.Lys330=
NR_033426.2:n.1236A=