Canonical Allele Identifier: CA15232103
Community Standard Title: NM_014049.5(ACAD9):c.555-116C>G
Gene: ACAD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128897516C>G , CM000665.2:g.128897516C>G GRCh38
NC_000003.11:g.128616359C>G , CM000665.1:g.128616359C>G GRCh37
NC_000003.10:g.130099049C>G NCBI36
NG_017064.1:g.23027C>G

Transcript Alleles

HGVS Amino-acid Change
NM_014049.5:c.555-116C>G MANE Select NP_054768.2:n.555-116C>G
ENST00000308982.12:c.555-116C>G MANE Select ENSP00000312618.7:n.555-116C>G
NM_014049.4:c.555-116C>G NP_054768.2:n.555-116C>G
NR_033426.1:n.933-116C>G
NR_033426.2:n.803-116C>G
ENST00000308982.11:c.555-116C>G ENSP00000312618.7:n.555-116C>G
ENST00000505192.5:c.*251-116C>G ENSP00000426277.1:n.*251-116C>G
ENST00000505867.5:c.*355-116C>G ENSP00000425346.1:n.*355-116C>G
ENST00000511227.5:c.*449-116C>G ENSP00000425226.1:n.*449-116C>G
ENST00000511325.2:n.633-116C>G
ENST00000512801.5:c.*251-116C>G ENSP00000427283.1:n.*251-116C>G
ENST00000514643.5:c.*251-116C>G ENSP00000422020.1:n.*251-116C>G
ENST00000679399.1:c.*449-116C>G ENSP00000505434.1:n.*449-116C>G
ENST00000679431.1:c.*427-116C>G ENSP00000506440.1:n.*427-116C>G
ENST00000679613.1:c.555-116C>G ENSP00000504971.1:n.555-116C>G
ENST00000679715.1:c.186-116C>G ENSP00000506228.1:n.186-116C>G
ENST00000679824.1:c.*1861-116C>G ENSP00000505516.1:n.*1861-116C>G
ENST00000679990.1:n.790-116C>G
ENST00000680636.1:c.555-116C>G ENSP00000504886.1:n.555-116C>G
ENST00000680744.1:c.555-116C>G ENSP00000505243.1:n.555-116C>G
ENST00000680764.1:c.*1955-116C>G ENSP00000505126.1:n.*1955-116C>G
ENST00000681319.1:n.633-116C>G
ENST00000681367.1:c.555-116C>G ENSP00000505309.1:n.555-116C>G
ENST00000681552.1:c.555-116C>G ENSP00000505699.1:n.555-116C>G
ENST00000681583.1:c.555-116C>G ENSP00000506340.1:n.555-116C>G
ENST00000681585.1:c.555-116C>G ENSP00000506316.1:n.555-116C>G
ENST00000681589.1:n.769-116C>G
ENST00000681784.1:n.633-116C>G
ENST00000681886.1:c.555-116C>G ENSP00000506500.1:n.555-116C>G
XM_011512742.1:c.186-116C>G XP_011511044.1:n.186-116C>G
XM_024453484.1:c.186-116C>G XP_024309252.1:n.186-116C>G
XM_024453485.1:c.186-116C>G XP_024309253.1:n.186-116C>G
XR_427367.1:n.627-116C>G
XR_427367.3:n.627-116C>G