Canonical Allele Identifier: CA1400926917
Gene: ACAD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128909392G= , CM000665.2:g.128909392G= GRCh38
NC_000003.11:g.128628235G= , CM000665.1:g.128628235G= GRCh37
NC_000003.10:g.130110925G= NCBI36
NG_017064.1:g.34903G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308982.12:c.1534G= MANE Select ENSP00000312618.7:p.Val512=
ENST00000511325.2:n.1612G=
ENST00000679399.1:c.*1705G= ENSP00000505434.1:n.*1705G=
ENST00000679431.1:c.*1410G= ENSP00000506440.1:n.*1410G=
ENST00000679613.1:c.1534G= ENSP00000504971.1:p.Val512=
ENST00000679715.1:c.1165G= ENSP00000506228.1:p.Val389=
ENST00000679824.1:c.*2840G= ENSP00000505516.1:n.*2840G=
ENST00000679990.1:n.1769G=
ENST00000680636.1:c.1534G= ENSP00000504886.1:p.Val512=
ENST00000680638.1:n.1287G=
ENST00000680744.1:c.*887G= ENSP00000505243.1:n.*887G=
ENST00000680764.1:c.*2938G= ENSP00000505126.1:n.*2938G=
ENST00000681319.1:n.2320G=
ENST00000681367.1:c.1534G= ENSP00000505309.1:p.Val512=
ENST00000681552.1:c.1150-3115G= ENSP00000505699.1:n.1150-3115G=
ENST00000681583.1:c.1534G= ENSP00000506340.1:p.Val512=
ENST00000681585.1:c.*153G= ENSP00000506316.1:n.*153G=
ENST00000681784.1:n.1612G=
ENST00000681886.1:c.*727G= ENSP00000506500.1:n.*727G=
ENST00000308982.11:c.1534G= ENSP00000312618.7:p.Val512=
ENST00000505867.5:c.*1334G= ENSP00000425346.1:n.*1334G=
ENST00000508971.1:c.823G= ENSP00000422683.1:p.Val275=
ENST00000511227.5:c.*1428G= ENSP00000425226.1:n.*1428G=
ENST00000511325.1:n.515G=
ENST00000511526.5:n.1067G=
NM_014049.4:c.1534G= NP_054768.2:p.Val512=
NR_033426.1:n.1912G=
XM_011512742.1:c.1165G= XP_011511044.1:p.Val389=
XM_024453484.1:c.1165G= XP_024309252.1:p.Val389=
XM_024453485.1:c.1165G= XP_024309253.1:p.Val389=
XR_427367.3:n.1610G=
NM_014049.5:c.1534G= MANE Select NP_054768.2:p.Val512=
NR_033426.2:n.1782G=