Canonical Allele Identifier: CA2667560517

Gene: ACAD9

Linked Data

• gnomAD v4: 3-128908115-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128908115C>A , CM000665.2:g.128908115C>A	GRCh38
NC_000003.11:g.128626958C>A , CM000665.1:g.128626958C>A	GRCh37
NC_000003.10:g.130109648C>A	NCBI36
NG_017064.1:g.33626C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1279-70C>A MANE Select	ENSP00000312618.7:n.1279-70C>A
ENST00000511325.2:n.1357-70C>A
ENST00000679399.1:c.*1380C>A	ENSP00000505434.1:n.*1380C>A
ENST00000679431.1:c.*1155-70C>A	ENSP00000506440.1:n.*1155-70C>A
ENST00000679613.1:c.1279-70C>A	ENSP00000504971.1:n.1279-70C>A
ENST00000679715.1:c.910-70C>A	ENSP00000506228.1:n.910-70C>A
ENST00000679824.1:c.*2585-70C>A	ENSP00000505516.1:n.*2585-70C>A
ENST00000679990.1:n.1514-70C>A
ENST00000680636.1:c.1279-70C>A	ENSP00000504886.1:n.1279-70C>A
ENST00000680638.1:n.254C>A
ENST00000680744.1:c.*632-70C>A	ENSP00000505243.1:n.*632-70C>A
ENST00000680764.1:c.*2683-70C>A	ENSP00000505126.1:n.*2683-70C>A
ENST00000681319.1:n.1357-70C>A
ENST00000681367.1:c.1279-70C>A	ENSP00000505309.1:n.1279-70C>A
ENST00000681552.1:c.1149+3610C>A	ENSP00000505699.1:n.1149+3610C>A
ENST00000681583.1:c.1279-70C>A	ENSP00000506340.1:n.1279-70C>A
ENST00000681585.1:c.1279-70C>A	ENSP00000506316.1:n.1279-70C>A
ENST00000681784.1:n.1357-70C>A
ENST00000681886.1:c.*472-70C>A	ENSP00000506500.1:n.*472-70C>A
ENST00000308982.11:c.1279-70C>A	ENSP00000312618.7:n.1279-70C>A
ENST00000505192.5:c.*975-70C>A	ENSP00000426277.1:n.*975-70C>A
ENST00000505867.5:c.*1079-70C>A	ENSP00000425346.1:n.*1079-70C>A
ENST00000508971.1:c.568-70C>A	ENSP00000422683.1:n.568-70C>A
ENST00000511227.5:c.*1173-70C>A	ENSP00000425226.1:n.*1173-70C>A
ENST00000511325.1:n.260-70C>A
ENST00000511526.5:n.812-70C>A
NM_014049.4:c.1279-70C>A	NP_054768.2:n.1279-70C>A
NR_033426.1:n.1657-70C>A
XM_011512742.1:c.910-70C>A	XP_011511044.1:n.910-70C>A
XR_427367.1:n.1355-70C>A
XM_024453484.1:c.910-70C>A	XP_024309252.1:n.910-70C>A
XM_024453485.1:c.910-70C>A	XP_024309253.1:n.910-70C>A
XR_427367.3:n.1355-70C>A
NM_014049.5:c.1279-70C>A MANE Select	NP_054768.2:n.1279-70C>A
NR_033426.2:n.1527-70C>A