Canonical Allele Identifier: CA354438604

Gene: ACAD9

Linked Data

• gnomAD v4: 3-128909399-C-T
• MyVariant Identifiers: chr3:g.128628242C>T (hg19) ; chr3:g.128909399C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1541C>T MANE Select	ENSP00000312618.7:p.Thr514Ile
ENST00000511325.2:n.1619C>T
ENST00000679399.1:c.*1712C>T	ENSP00000505434.1:n.*1712C>T
ENST00000679431.1:c.*1417C>T	ENSP00000506440.1:n.*1417C>T
ENST00000679613.1:c.1541C>T	ENSP00000504971.1:p.Thr514Ile
ENST00000679715.1:c.1172C>T	ENSP00000506228.1:p.Thr391Ile
ENST00000679824.1:c.*2847C>T	ENSP00000505516.1:n.*2847C>T
ENST00000679990.1:n.1776C>T
ENST00000680636.1:c.1541C>T	ENSP00000504886.1:p.Thr514Ile
ENST00000680638.1:n.1294C>T
ENST00000680744.1:c.*894C>T	ENSP00000505243.1:n.*894C>T
ENST00000680764.1:c.*2945C>T	ENSP00000505126.1:n.*2945C>T
ENST00000681319.1:n.2327C>T
ENST00000681367.1:c.1541C>T	ENSP00000505309.1:p.Thr514Ile
ENST00000681552.1:c.1150-3108C>T	ENSP00000505699.1:n.1150-3108C>T
ENST00000681583.1:c.1541C>T	ENSP00000506340.1:p.Thr514Ile
ENST00000681585.1:c.*160C>T	ENSP00000506316.1:n.*160C>T
ENST00000681784.1:n.1619C>T
ENST00000681886.1:c.*734C>T	ENSP00000506500.1:n.*734C>T
ENST00000308982.11:c.1541C>T	ENSP00000312618.7:p.Thr514Ile
ENST00000505867.5:c.*1341C>T	ENSP00000425346.1:n.*1341C>T
ENST00000508971.1:c.830C>T	ENSP00000422683.1:p.Thr277Ile
ENST00000511227.5:c.*1435C>T	ENSP00000425226.1:n.*1435C>T
ENST00000511325.1:n.522C>T
ENST00000511526.5:n.1074C>T
NM_014049.4:c.1541C>T	NP_054768.2:p.Thr514Ile
NR_033426.1:n.1919C>T
XM_011512742.1:c.1172C>T	XP_011511044.1:p.Thr391Ile
XM_024453484.1:c.1172C>T	XP_024309252.1:p.Thr391Ile
XM_024453485.1:c.1172C>T	XP_024309253.1:p.Thr391Ile
XR_427367.3:n.1617C>T
NM_014049.5:c.1541C>T MANE Select	NP_054768.2:p.Thr514Ile
NR_033426.2:n.1789C>T