Canonical Allele Identifier: CA82537734

Gene: ACAD9

Linked Data

• dbSNP Id: rs928864946
• gnomAD v4: 3-128909467-T-C
• MyVariant Identifiers: chr3:g.128628310T>C (hg19) ; chr3:g.128909467T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909467T>C , CM000665.2:g.128909467T>C	GRCh38
NC_000003.11:g.128628310T>C , CM000665.1:g.128628310T>C	GRCh37
NC_000003.10:g.130111000T>C	NCBI36
NG_017064.1:g.34978T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1563+46T>C MANE Select	ENSP00000312618.7:n.1563+46T>C
ENST00000511325.2:n.1687T>C
ENST00000679399.1:c.*1734+46T>C	ENSP00000505434.1:n.*1734+46T>C
ENST00000679431.1:c.*1439+46T>C	ENSP00000506440.1:n.*1439+46T>C
ENST00000679613.1:c.1563+46T>C	ENSP00000504971.1:n.1563+46T>C
ENST00000679715.1:c.1194+46T>C	ENSP00000506228.1:n.1194+46T>C
ENST00000679824.1:c.*2869+46T>C	ENSP00000505516.1:n.*2869+46T>C
ENST00000679990.1:n.1844T>C
ENST00000680636.1:c.1563+46T>C	ENSP00000504886.1:n.1563+46T>C
ENST00000680638.1:n.1362T>C
ENST00000680744.1:c.*916+46T>C	ENSP00000505243.1:n.*916+46T>C
ENST00000680764.1:c.*2967+46T>C	ENSP00000505126.1:n.*2967+46T>C
ENST00000681319.1:n.2349+46T>C
ENST00000681367.1:c.1563+46T>C	ENSP00000505309.1:n.1563+46T>C
ENST00000681552.1:c.1150-3040T>C	ENSP00000505699.1:n.1150-3040T>C
ENST00000681583.1:c.1563+46T>C	ENSP00000506340.1:n.1563+46T>C
ENST00000681585.1:c.*182+46T>C	ENSP00000506316.1:n.*182+46T>C
ENST00000681784.1:n.1687T>C
ENST00000681886.1:c.*802T>C	ENSP00000506500.1:n.*802T>C
ENST00000308982.11:c.1563+46T>C	ENSP00000312618.7:n.1563+46T>C
ENST00000505867.5:c.*1363+46T>C	ENSP00000425346.1:n.*1363+46T>C
ENST00000508971.1:c.852+46T>C	ENSP00000422683.1:n.852+46T>C
ENST00000511227.5:c.*1457+46T>C	ENSP00000425226.1:n.*1457+46T>C
ENST00000511325.1:n.590T>C
ENST00000511526.5:n.1096+46T>C
NM_014049.4:c.1563+46T>C	NP_054768.2:n.1563+46T>C
NR_033426.1:n.1941+46T>C
XM_011512742.1:c.1194+46T>C	XP_011511044.1:n.1194+46T>C
XM_024453484.1:c.1194+46T>C	XP_024309252.1:n.1194+46T>C
XM_024453485.1:c.1194+46T>C	XP_024309253.1:n.1194+46T>C
XR_427367.3:n.1639+46T>C
NM_014049.5:c.1563+46T>C MANE Select	NP_054768.2:n.1563+46T>C
NR_033426.2:n.1811+46T>C