Canonical Allele Identifier: CA2667561348
Gene: ACAD9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128909420_128909428del , CM000665.2:g.128909420_128909428del GRCh38
NC_000003.11:g.128628263_128628271del , CM000665.1:g.128628263_128628271del GRCh37
NC_000003.10:g.130110953_130110961del NCBI36
NG_017064.1:g.34931_34939del

Transcript Alleles

HGVS Amino-acid Change
ENST00000308982.12:c.1562_1563+7del
ENST00000511325.2:n.1640_1648del
ENST00000679399.1:c.*1733_*1734+7del
ENST00000679431.1:c.*1438_*1439+7del
ENST00000679613.1:c.1562_1563+7del
ENST00000679715.1:c.1193_1194+7del
ENST00000679824.1:c.*2868_*2869+7del
ENST00000679990.1:n.1797_1805del
ENST00000680636.1:c.1562_1563+7del
ENST00000680638.1:n.1315_1323del
ENST00000680744.1:c.*915_*916+7del
ENST00000680764.1:c.*2966_*2967+7del
ENST00000681319.1:n.2348_2349+7del
ENST00000681367.1:c.1562_1563+7del
ENST00000681552.1:c.1150-3087_1150-3079del ENSP00000505699.1:n.1150-3087_1150-3079del
ENST00000681583.1:c.1562_1563+7del
ENST00000681585.1:c.*181_*182+7del
ENST00000681784.1:n.1640_1648del
ENST00000681886.1:c.*755_*763del ENSP00000506500.1:n.*755_*763del
ENST00000308982.11:c.1562_1563+7del
ENST00000505867.5:c.*1362_*1363+7del
ENST00000508971.1:c.851_852+7del
ENST00000511227.5:c.*1456_*1457+7del
ENST00000511325.1:n.543_551del
ENST00000511526.5:n.1095_1096+7del
NM_014049.4:c.1562_1563+7del
NR_033426.1:n.1940_1941+7del
XM_011512742.1:c.1193_1194+7del
XM_024453484.1:c.1193_1194+7del
XM_024453485.1:c.1193_1194+7del
XR_427367.3:n.1638_1639+7del
NM_014049.5:c.1562_1563+7del
NR_033426.2:n.1810_1811+7del