Canonical Allele Identifier: CA354438606

Gene: ACAD9

Linked Data

• MyVariant Identifiers: chr3:g.128628242C>A (hg19) ; chr3:g.128909399C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909399C>A , CM000665.2:g.128909399C>A	GRCh38
NC_000003.11:g.128628242C>A , CM000665.1:g.128628242C>A	GRCh37
NC_000003.10:g.130110932C>A	NCBI36
NG_017064.1:g.34910C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1541C>A MANE Select	ENSP00000312618.7:p.Thr514Lys
ENST00000511325.2:n.1619C>A
ENST00000679399.1:c.*1712C>A	ENSP00000505434.1:n.*1712C>A
ENST00000679431.1:c.*1417C>A	ENSP00000506440.1:n.*1417C>A
ENST00000679613.1:c.1541C>A	ENSP00000504971.1:p.Thr514Lys
ENST00000679715.1:c.1172C>A	ENSP00000506228.1:p.Thr391Lys
ENST00000679824.1:c.*2847C>A	ENSP00000505516.1:n.*2847C>A
ENST00000679990.1:n.1776C>A
ENST00000680636.1:c.1541C>A	ENSP00000504886.1:p.Thr514Lys
ENST00000680638.1:n.1294C>A
ENST00000680744.1:c.*894C>A	ENSP00000505243.1:n.*894C>A
ENST00000680764.1:c.*2945C>A	ENSP00000505126.1:n.*2945C>A
ENST00000681319.1:n.2327C>A
ENST00000681367.1:c.1541C>A	ENSP00000505309.1:p.Thr514Lys
ENST00000681552.1:c.1150-3108C>A	ENSP00000505699.1:n.1150-3108C>A
ENST00000681583.1:c.1541C>A	ENSP00000506340.1:p.Thr514Lys
ENST00000681585.1:c.*160C>A	ENSP00000506316.1:n.*160C>A
ENST00000681784.1:n.1619C>A
ENST00000681886.1:c.*734C>A	ENSP00000506500.1:n.*734C>A
ENST00000308982.11:c.1541C>A	ENSP00000312618.7:p.Thr514Lys
ENST00000505867.5:c.*1341C>A	ENSP00000425346.1:n.*1341C>A
ENST00000508971.1:c.830C>A	ENSP00000422683.1:p.Thr277Lys
ENST00000511227.5:c.*1435C>A	ENSP00000425226.1:n.*1435C>A
ENST00000511325.1:n.522C>A
ENST00000511526.5:n.1074C>A
NM_014049.4:c.1541C>A	NP_054768.2:p.Thr514Lys
NR_033426.1:n.1919C>A
XM_011512742.1:c.1172C>A	XP_011511044.1:p.Thr391Lys
XM_024453484.1:c.1172C>A	XP_024309252.1:p.Thr391Lys
XM_024453485.1:c.1172C>A	XP_024309253.1:p.Thr391Lys
XR_427367.3:n.1617C>A
NM_014049.5:c.1541C>A MANE Select	NP_054768.2:p.Thr514Lys
NR_033426.2:n.1789C>A