Canonical Allele Identifier: CA435591804
Gene: ACAD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1100820
ClinVar RCV Id: RCV001423558
dbSNP Id: rs1274484021
MyVariant Identifiers: chr3:g.128622972T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128904129T>C , CM000665.2:g.128904129T>C GRCh38
NC_000003.11:g.128622972T>C , CM000665.1:g.128622972T>C GRCh37
NC_000003.10:g.130105662T>C NCBI36
NG_017064.1:g.29640T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000308982.12:c.1026T>C MANE Select ENSP00000312618.7:p.Ile342=
ENST00000511325.2:n.1104T>C
ENST00000679399.1:c.*920T>C ENSP00000505434.1:n.*920T>C
ENST00000679431.1:c.*902T>C ENSP00000506440.1:n.*902T>C
ENST00000679613.1:c.1026T>C ENSP00000504971.1:p.Ile342=
ENST00000679715.1:c.657T>C ENSP00000506228.1:p.Ile219=
ENST00000679824.1:c.*2332T>C ENSP00000505516.1:n.*2332T>C
ENST00000679990.1:n.1261T>C
ENST00000680636.1:c.1026T>C ENSP00000504886.1:p.Ile342=
ENST00000680744.1:c.*379T>C ENSP00000505243.1:n.*379T>C
ENST00000680764.1:c.*2430T>C ENSP00000505126.1:n.*2430T>C
ENST00000681319.1:n.1104T>C
ENST00000681367.1:c.1026T>C ENSP00000505309.1:p.Ile342=
ENST00000681552.1:c.1026T>C ENSP00000505699.1:p.Ile342=
ENST00000681583.1:c.1026T>C ENSP00000506340.1:p.Ile342=
ENST00000681585.1:c.1026T>C ENSP00000506316.1:p.Ile342=
ENST00000681589.1:n.1240T>C
ENST00000681784.1:n.1104T>C
ENST00000681886.1:c.*219T>C ENSP00000506500.1:n.*219T>C
ENST00000308982.11:c.1026T>C ENSP00000312618.7:p.Ile342=
ENST00000505192.5:c.*722T>C ENSP00000426277.1:n.*722T>C
ENST00000505867.5:c.*826T>C ENSP00000425346.1:n.*826T>C
ENST00000508971.1:c.315T>C ENSP00000422683.1:p.Ile105=
ENST00000511227.5:c.*920T>C ENSP00000425226.1:n.*920T>C
ENST00000511526.5:n.531T>C
NM_014049.4:c.1026T>C NP_054768.2:p.Ile342=
NR_033426.1:n.1404T>C
XM_011512742.1:c.657T>C XP_011511044.1:p.Ile219=
XR_427367.1:n.1102T>C
XM_024453484.1:c.657T>C XP_024309252.1:p.Ile219=
XM_024453485.1:c.657T>C XP_024309253.1:p.Ile219=
XR_427367.3:n.1102T>C
NM_014049.5:c.1026T>C MANE Select NP_054768.2:p.Ile342=
NR_033426.2:n.1274T>C