Canonical Allele Identifier: CA1400924340

Gene: ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128904086_128904087delinsCA , CM000665.2:g.128904086_128904087delinsCA	GRCh38
NC_000003.11:g.128622929_128622930delinsCA , CM000665.1:g.128622929_128622930delinsCA	GRCh37
NC_000003.10:g.130105619_130105620delinsCA	NCBI36
NG_017064.1:g.29597_29598delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.983_984delinsCA MANE Select	ENSP00000312618.7:p.Thr328=
ENST00000511325.2:n.1061_1062delinsCA
ENST00000679399.1:c.*877_*878delinsCA	ENSP00000505434.1:n.*877_*878delinsCA
ENST00000679431.1:c.*859_*860delinsCA	ENSP00000506440.1:n.*859_*860delinsCA
ENST00000679613.1:c.983_984delinsCA	ENSP00000504971.1:p.Thr328=
ENST00000679715.1:c.614_615delinsCA	ENSP00000506228.1:p.Thr205=
ENST00000679824.1:c.*2289_*2290delinsCA	ENSP00000505516.1:n.*2289_*2290delinsCA
ENST00000679990.1:n.1218_1219delinsCA
ENST00000680636.1:c.983_984delinsCA	ENSP00000504886.1:p.Thr328=
ENST00000680744.1:c.*336_*337delinsCA	ENSP00000505243.1:n.*336_*337delinsCA
ENST00000680764.1:c.*2387_*2388delinsCA	ENSP00000505126.1:n.*2387_*2388delinsCA
ENST00000681319.1:n.1061_1062delinsCA
ENST00000681367.1:c.983_984delinsCA	ENSP00000505309.1:p.Thr328=
ENST00000681552.1:c.983_984delinsCA	ENSP00000505699.1:p.Thr328=
ENST00000681583.1:c.983_984delinsCA	ENSP00000506340.1:p.Thr328=
ENST00000681585.1:c.983_984delinsCA	ENSP00000506316.1:p.Thr328=
ENST00000681589.1:n.1197_1198delinsCA
ENST00000681784.1:n.1061_1062delinsCA
ENST00000681886.1:c.*176_*177delinsCA	ENSP00000506500.1:n.*176_*177delinsCA
ENST00000308982.11:c.983_984delinsCA	ENSP00000312618.7:p.Thr328=
ENST00000505192.5:c.*679_*680delinsCA	ENSP00000426277.1:n.*679_*680delinsCA
ENST00000505867.5:c.*783_*784delinsCA	ENSP00000425346.1:n.*783_*784delinsCA
ENST00000508971.1:c.272_273delinsCA	ENSP00000422683.1:p.Thr91=
ENST00000511227.5:c.*877_*878delinsCA	ENSP00000425226.1:n.*877_*878delinsCA
ENST00000511526.5:n.488_489delinsCA
NM_014049.4:c.983_984delinsCA	NP_054768.2:p.Thr328=
NR_033426.1:n.1361_1362delinsCA
XM_011512742.1:c.614_615delinsCA	XP_011511044.1:p.Thr205=
XR_427367.1:n.1059_1060delinsCA
XM_024453484.1:c.614_615delinsCA	XP_024309252.1:p.Thr205=
XM_024453485.1:c.614_615delinsCA	XP_024309253.1:p.Thr205=
XR_427367.3:n.1059_1060delinsCA
NM_014049.5:c.983_984delinsCA MANE Select	NP_054768.2:p.Thr328=
NR_033426.2:n.1231_1232delinsCA