Canonical Allele Identifier: CA546182253

Gene: ACAD9

Linked Data

• dbSNP Id: rs1243790486
• gnomAD v2: 3-128627017-ACTG-A
• gnomAD v4: 3-128908174-ACTG-A
• MyVariant Identifiers: chr3:g.128627018_128627020del (hg19) ; chr3:g.128908175_128908177del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128908175_128908177del , CM000665.2:g.128908175_128908177del	GRCh38
NC_000003.11:g.128627018_128627020del , CM000665.1:g.128627018_128627020del	GRCh37
NC_000003.10:g.130109708_130109710del	NCBI36
NG_017064.1:g.33686_33688del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1279-10_1279-8del MANE Select	ENSP00000312618.7:n.1279-10_1279-8del
ENST00000511325.2:n.1357-10_1357-8del
ENST00000679399.1:c.*1440_*1442del	ENSP00000505434.1:n.*1440_*1442del
ENST00000679431.1:c.*1155-10_*1155-8del	ENSP00000506440.1:n.*1155-10_*1155-8del
ENST00000679613.1:c.1279-10_1279-8del	ENSP00000504971.1:n.1279-10_1279-8del
ENST00000679715.1:c.910-10_910-8del	ENSP00000506228.1:n.910-10_910-8del
ENST00000679824.1:c.*2585-10_*2585-8del	ENSP00000505516.1:n.*2585-10_*2585-8del
ENST00000679990.1:n.1514-10_1514-8del
ENST00000680636.1:c.1279-10_1279-8del	ENSP00000504886.1:n.1279-10_1279-8del
ENST00000680638.1:n.314_316del
ENST00000680744.1:c.*632-10_*632-8del	ENSP00000505243.1:n.*632-10_*632-8del
ENST00000680764.1:c.*2683-10_*2683-8del	ENSP00000505126.1:n.*2683-10_*2683-8del
ENST00000681319.1:n.1357-10_1357-8del
ENST00000681367.1:c.1279-10_1279-8del	ENSP00000505309.1:n.1279-10_1279-8del
ENST00000681552.1:c.1149+3670_1149+3672del	ENSP00000505699.1:n.1149+3670_1149+3672del
ENST00000681583.1:c.1279-10_1279-8del	ENSP00000506340.1:n.1279-10_1279-8del
ENST00000681585.1:c.1279-10_1279-8del	ENSP00000506316.1:n.1279-10_1279-8del
ENST00000681784.1:n.1357-10_1357-8del
ENST00000681886.1:c.*472-10_*472-8del	ENSP00000506500.1:n.*472-10_*472-8del
ENST00000308982.11:c.1279-10_1279-8del	ENSP00000312618.7:n.1279-10_1279-8del
ENST00000505192.5:c.*975-10_*975-8del	ENSP00000426277.1:n.*975-10_*975-8del
ENST00000505867.5:c.*1079-10_*1079-8del	ENSP00000425346.1:n.*1079-10_*1079-8del
ENST00000508971.1:c.568-10_568-8del	ENSP00000422683.1:n.568-10_568-8del
ENST00000511227.5:c.*1173-10_*1173-8del	ENSP00000425226.1:n.*1173-10_*1173-8del
ENST00000511325.1:n.260-10_260-8del
ENST00000511526.5:n.812-10_812-8del
NM_014049.4:c.1279-10_1279-8del	NP_054768.2:n.1279-10_1279-8del
NR_033426.1:n.1657-10_1657-8del
XM_011512742.1:c.910-10_910-8del	XP_011511044.1:n.910-10_910-8del
XR_427367.1:n.1355-10_1355-8del
XM_024453484.1:c.910-10_910-8del	XP_024309252.1:n.910-10_910-8del
XM_024453485.1:c.910-10_910-8del	XP_024309253.1:n.910-10_910-8del
XR_427367.3:n.1355-10_1355-8del
NM_014049.5:c.1279-10_1279-8del MANE Select	NP_054768.2:n.1279-10_1279-8del
NR_033426.2:n.1527-10_1527-8del