Canonical Allele Identifier: CA1400924314
Gene: ACAD9 HGNC NCBI

Linked Data

dbSNP Id: rs1935817168

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128904023A>C , CM000665.2:g.128904023A>C GRCh38
NC_000003.11:g.128622866A>C , CM000665.1:g.128622866A>C GRCh37
NC_000003.10:g.130105556A>C NCBI36
NG_017064.1:g.29534A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000308982.12:c.959-39A>C MANE Select ENSP00000312618.7:n.959-39A>C
ENST00000511325.2:n.1037-39A>C
ENST00000679399.1:c.*853-39A>C ENSP00000505434.1:n.*853-39A>C
ENST00000679431.1:c.*835-39A>C ENSP00000506440.1:n.*835-39A>C
ENST00000679613.1:c.959-39A>C ENSP00000504971.1:n.959-39A>C
ENST00000679715.1:c.590-39A>C ENSP00000506228.1:n.590-39A>C
ENST00000679824.1:c.*2265-39A>C ENSP00000505516.1:n.*2265-39A>C
ENST00000679990.1:n.1194-39A>C
ENST00000680636.1:c.959-39A>C ENSP00000504886.1:n.959-39A>C
ENST00000680744.1:c.*312-39A>C ENSP00000505243.1:n.*312-39A>C
ENST00000680764.1:c.*2363-39A>C ENSP00000505126.1:n.*2363-39A>C
ENST00000681319.1:n.1037-39A>C
ENST00000681367.1:c.959-39A>C ENSP00000505309.1:n.959-39A>C
ENST00000681552.1:c.959-39A>C ENSP00000505699.1:n.959-39A>C
ENST00000681583.1:c.959-39A>C ENSP00000506340.1:n.959-39A>C
ENST00000681585.1:c.959-39A>C ENSP00000506316.1:n.959-39A>C
ENST00000681589.1:n.1173-39A>C
ENST00000681784.1:n.1037-39A>C
ENST00000681886.1:c.*152-39A>C ENSP00000506500.1:n.*152-39A>C
ENST00000308982.11:c.959-39A>C ENSP00000312618.7:n.959-39A>C
ENST00000505192.5:c.*655-39A>C ENSP00000426277.1:n.*655-39A>C
ENST00000505867.5:c.*759-39A>C ENSP00000425346.1:n.*759-39A>C
ENST00000508971.1:c.248-39A>C ENSP00000422683.1:n.248-39A>C
ENST00000511227.5:c.*853-39A>C ENSP00000425226.1:n.*853-39A>C
ENST00000511526.5:n.464-39A>C
NM_014049.4:c.959-39A>C NP_054768.2:n.959-39A>C
NR_033426.1:n.1337-39A>C
XM_011512742.1:c.590-39A>C XP_011511044.1:n.590-39A>C
XR_427367.1:n.1035-39A>C
XM_024453484.1:c.590-39A>C XP_024309252.1:n.590-39A>C
XM_024453485.1:c.590-39A>C XP_024309253.1:n.590-39A>C
XR_427367.3:n.1035-39A>C
NM_014049.5:c.959-39A>C MANE Select NP_054768.2:n.959-39A>C
NR_033426.2:n.1207-39A>C