Canonical Allele Identifier: CA354438643

Gene: ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128628264G>C (hg19) ; chr3:g.128909421G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909421G>C , CM000665.2:g.128909421G>C	GRCh38
NC_000003.11:g.128628264G>C , CM000665.1:g.128628264G>C	GRCh37
NC_000003.10:g.130110954G>C	NCBI36
NG_017064.1:g.34932G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1563G>C MANE Select	ENSP00000312618.7:p.Lys521Asn
ENST00000511325.2:n.1641G>C
ENST00000679399.1:c.*1734G>C	ENSP00000505434.1:n.*1734G>C
ENST00000679431.1:c.*1439G>C	ENSP00000506440.1:n.*1439G>C
ENST00000679613.1:c.1563G>C	ENSP00000504971.1:p.Lys521Asn
ENST00000679715.1:c.1194G>C	ENSP00000506228.1:p.Lys398Asn
ENST00000679824.1:c.*2869G>C	ENSP00000505516.1:n.*2869G>C
ENST00000679990.1:n.1798G>C
ENST00000680636.1:c.1563G>C	ENSP00000504886.1:p.Lys521Asn
ENST00000680638.1:n.1316G>C
ENST00000680744.1:c.*916G>C	ENSP00000505243.1:n.*916G>C
ENST00000680764.1:c.*2967G>C	ENSP00000505126.1:n.*2967G>C
ENST00000681319.1:n.2349G>C
ENST00000681367.1:c.1563G>C	ENSP00000505309.1:p.Lys521Asn
ENST00000681552.1:c.1150-3086G>C	ENSP00000505699.1:n.1150-3086G>C
ENST00000681583.1:c.1563G>C	ENSP00000506340.1:p.Lys521Asn
ENST00000681585.1:c.*182G>C	ENSP00000506316.1:n.*182G>C
ENST00000681784.1:n.1641G>C
ENST00000681886.1:c.*756G>C	ENSP00000506500.1:n.*756G>C
ENST00000308982.11:c.1563G>C	ENSP00000312618.7:p.Lys521Asn
ENST00000505867.5:c.*1363G>C	ENSP00000425346.1:n.*1363G>C
ENST00000508971.1:c.852G>C	ENSP00000422683.1:p.Lys284Asn
ENST00000511227.5:c.*1457G>C	ENSP00000425226.1:n.*1457G>C
ENST00000511325.1:n.544G>C
ENST00000511526.5:n.1096G>C
NM_014049.4:c.1563G>C	NP_054768.2:p.Lys521Asn
NR_033426.1:n.1941G>C
XM_011512742.1:c.1194G>C	XP_011511044.1:p.Lys398Asn
XM_024453484.1:c.1194G>C	XP_024309252.1:p.Lys398Asn
XM_024453485.1:c.1194G>C	XP_024309253.1:p.Lys398Asn
XR_427367.3:n.1639G>C
NM_014049.5:c.1563G>C MANE Select	NP_054768.2:p.Lys521Asn
NR_033426.2:n.1811G>C