Canonical Allele Identifier: CA354436069

Gene: ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128622971T>C (hg19) ; chr3:g.128904128T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128904128T>C , CM000665.2:g.128904128T>C	GRCh38
NC_000003.11:g.128622971T>C , CM000665.1:g.128622971T>C	GRCh37
NC_000003.10:g.130105661T>C	NCBI36
NG_017064.1:g.29639T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1025T>C MANE Select	ENSP00000312618.7:p.Ile342Thr
ENST00000511325.2:n.1103T>C
ENST00000679399.1:c.*919T>C	ENSP00000505434.1:n.*919T>C
ENST00000679431.1:c.*901T>C	ENSP00000506440.1:n.*901T>C
ENST00000679613.1:c.1025T>C	ENSP00000504971.1:p.Ile342Thr
ENST00000679715.1:c.656T>C	ENSP00000506228.1:p.Ile219Thr
ENST00000679824.1:c.*2331T>C	ENSP00000505516.1:n.*2331T>C
ENST00000679990.1:n.1260T>C
ENST00000680636.1:c.1025T>C	ENSP00000504886.1:p.Ile342Thr
ENST00000680744.1:c.*378T>C	ENSP00000505243.1:n.*378T>C
ENST00000680764.1:c.*2429T>C	ENSP00000505126.1:n.*2429T>C
ENST00000681319.1:n.1103T>C
ENST00000681367.1:c.1025T>C	ENSP00000505309.1:p.Ile342Thr
ENST00000681552.1:c.1025T>C	ENSP00000505699.1:p.Ile342Thr
ENST00000681583.1:c.1025T>C	ENSP00000506340.1:p.Ile342Thr
ENST00000681585.1:c.1025T>C	ENSP00000506316.1:p.Ile342Thr
ENST00000681589.1:n.1239T>C
ENST00000681784.1:n.1103T>C
ENST00000681886.1:c.*218T>C	ENSP00000506500.1:n.*218T>C
ENST00000308982.11:c.1025T>C	ENSP00000312618.7:p.Ile342Thr
ENST00000505192.5:c.*721T>C	ENSP00000426277.1:n.*721T>C
ENST00000505867.5:c.*825T>C	ENSP00000425346.1:n.*825T>C
ENST00000508971.1:c.314T>C	ENSP00000422683.1:p.Ile105Thr
ENST00000511227.5:c.*919T>C	ENSP00000425226.1:n.*919T>C
ENST00000511526.5:n.530T>C
NM_014049.4:c.1025T>C	NP_054768.2:p.Ile342Thr
NR_033426.1:n.1403T>C
XM_011512742.1:c.656T>C	XP_011511044.1:p.Ile219Thr
XR_427367.1:n.1101T>C
XM_024453484.1:c.656T>C	XP_024309252.1:p.Ile219Thr
XM_024453485.1:c.656T>C	XP_024309253.1:p.Ile219Thr
XR_427367.3:n.1101T>C
NM_014049.5:c.1025T>C MANE Select	NP_054768.2:p.Ile342Thr
NR_033426.2:n.1273T>C