Canonical Allele Identifier: CA546182897

Gene: ACAD9

Linked Data

• dbSNP Id: rs1260441712
• gnomAD v2: 3-128628362-T-TAGAAC
• gnomAD v3: 3-128909519-T-TAGAAC
• gnomAD v4: 3-128909519-T-TAGAAC
• MyVariant Identifiers: chr3:g.128628362_128628363insAGAAC (hg19) ; chr3:g.128909519_128909520insAGAAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128909524_128909528dup , CM000665.2:g.128909524_128909528dup	GRCh38
NC_000003.11:g.128628367_128628371dup , CM000665.1:g.128628367_128628371dup	GRCh37
NC_000003.10:g.130111057_130111061dup	NCBI36
NG_017064.1:g.35035_35039dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1563+103_1563+107dup MANE Select	ENSP00000312618.7:n.1563+103_1563+107dup
ENST00000511325.2:n.1744_1748dup
ENST00000679399.1:c.*1734+103_*1734+107dup	ENSP00000505434.1:n.*1734+103_*1734+107dup
ENST00000679431.1:c.*1439+103_*1439+107dup	ENSP00000506440.1:n.*1439+103_*1439+107dup
ENST00000679613.1:c.1563+103_1563+107dup	ENSP00000504971.1:n.1563+103_1563+107dup
ENST00000679715.1:c.1194+103_1194+107dup	ENSP00000506228.1:n.1194+103_1194+107dup
ENST00000679824.1:c.*2869+103_*2869+107dup	ENSP00000505516.1:n.*2869+103_*2869+107dup
ENST00000679990.1:n.1901_1905dup
ENST00000680636.1:c.1563+103_1563+107dup	ENSP00000504886.1:n.1563+103_1563+107dup
ENST00000680638.1:n.1419_1423dup
ENST00000680744.1:c.*916+103_*916+107dup	ENSP00000505243.1:n.*916+103_*916+107dup
ENST00000680764.1:c.*2967+103_*2967+107dup	ENSP00000505126.1:n.*2967+103_*2967+107dup
ENST00000681319.1:n.2349+103_2349+107dup
ENST00000681367.1:c.1563+103_1563+107dup	ENSP00000505309.1:n.1563+103_1563+107dup
ENST00000681552.1:c.1150-2983_1150-2979dup	ENSP00000505699.1:n.1150-2983_1150-2979dup
ENST00000681583.1:c.1563+103_1563+107dup	ENSP00000506340.1:n.1563+103_1563+107dup
ENST00000681585.1:c.*182+103_*182+107dup	ENSP00000506316.1:n.*182+103_*182+107dup
ENST00000681784.1:n.1744_1748dup
ENST00000681886.1:c.*859_*863dup	ENSP00000506500.1:n.*859_*863dup
ENST00000308982.11:c.1563+103_1563+107dup	ENSP00000312618.7:n.1563+103_1563+107dup
ENST00000505867.5:c.*1363+103_*1363+107dup	ENSP00000425346.1:n.*1363+103_*1363+107dup
ENST00000508971.1:c.852+103_852+107dup	ENSP00000422683.1:n.852+103_852+107dup
ENST00000511227.5:c.*1457+103_*1457+107dup	ENSP00000425226.1:n.*1457+103_*1457+107dup
ENST00000511325.1:n.647_651dup
ENST00000511526.5:n.1096+103_1096+107dup
NM_014049.4:c.1563+103_1563+107dup	NP_054768.2:n.1563+103_1563+107dup
NR_033426.1:n.1941+103_1941+107dup
XM_011512742.1:c.1194+103_1194+107dup	XP_011511044.1:n.1194+103_1194+107dup
XM_024453484.1:c.1194+103_1194+107dup	XP_024309252.1:n.1194+103_1194+107dup
XM_024453485.1:c.1194+103_1194+107dup	XP_024309253.1:n.1194+103_1194+107dup
XR_427367.3:n.1639+103_1639+107dup
NM_014049.5:c.1563+103_1563+107dup MANE Select	NP_054768.2:n.1563+103_1563+107dup
NR_033426.2:n.1811+103_1811+107dup