Canonical Allele Identifier: CA898718319

Gene: ACAD9

Linked Data

• dbSNP Id: rs1439248620
• gnomAD v3: 3-128902376-T-G
• gnomAD v4: 3-128902376-T-G
• MyVariant Identifiers: chr3:g.128621219T>G (hg19) ; chr3:g.128902376T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128902376T>G , CM000665.2:g.128902376T>G	GRCh38
NC_000003.11:g.128621219T>G , CM000665.1:g.128621219T>G	GRCh37
NC_000003.10:g.130103909T>G	NCBI36
NG_017064.1:g.27887T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.883-177T>G MANE Select	ENSP00000312618.7:n.883-177T>G
ENST00000511325.2:n.961-177T>G
ENST00000679399.1:c.*777-177T>G	ENSP00000505434.1:n.*777-177T>G
ENST00000679431.1:c.*755-177T>G	ENSP00000506440.1:n.*755-177T>G
ENST00000679613.1:c.883-177T>G	ENSP00000504971.1:n.883-177T>G
ENST00000679715.1:c.514-177T>G	ENSP00000506228.1:n.514-177T>G
ENST00000679824.1:c.*2189-177T>G	ENSP00000505516.1:n.*2189-177T>G
ENST00000679990.1:n.1118-177T>G
ENST00000680636.1:c.883-177T>G	ENSP00000504886.1:n.883-177T>G
ENST00000680744.1:c.*236-177T>G	ENSP00000505243.1:n.*236-177T>G
ENST00000680764.1:c.*2283-177T>G	ENSP00000505126.1:n.*2283-177T>G
ENST00000681319.1:n.961-177T>G
ENST00000681367.1:c.883-177T>G	ENSP00000505309.1:n.883-177T>G
ENST00000681552.1:c.883-177T>G	ENSP00000505699.1:n.883-177T>G
ENST00000681583.1:c.883-177T>G	ENSP00000506340.1:n.883-177T>G
ENST00000681585.1:c.883-177T>G	ENSP00000506316.1:n.883-177T>G
ENST00000681589.1:n.1097-177T>G
ENST00000681784.1:n.961-177T>G
ENST00000681886.1:c.*76-177T>G	ENSP00000506500.1:n.*76-177T>G
ENST00000308982.11:c.883-177T>G	ENSP00000312618.7:n.883-177T>G
ENST00000505192.5:c.*579-177T>G	ENSP00000426277.1:n.*579-177T>G
ENST00000505867.5:c.*683-177T>G	ENSP00000425346.1:n.*683-177T>G
ENST00000508971.1:c.172-177T>G	ENSP00000422683.1:n.172-177T>G
ENST00000511227.5:c.*777-177T>G	ENSP00000425226.1:n.*777-177T>G
ENST00000511526.5:n.384-177T>G
NM_014049.4:c.883-177T>G	NP_054768.2:n.883-177T>G
NR_033426.1:n.1261-177T>G
XM_011512742.1:c.514-177T>G	XP_011511044.1:n.514-177T>G
XR_427367.1:n.955-177T>G
XM_024453484.1:c.514-177T>G	XP_024309252.1:n.514-177T>G
XM_024453485.1:c.514-177T>G	XP_024309253.1:n.514-177T>G
XR_427367.3:n.955-177T>G
NM_014049.5:c.883-177T>G MANE Select	NP_054768.2:n.883-177T>G
NR_033426.2:n.1131-177T>G