Canonical Allele Identifier: CA82531943

Gene: ACAD9

Linked Data

• dbSNP Id: rs759491530
• gnomAD v2: 3-128621668-CCT-C
• gnomAD v3: 3-128902825-CCT-C
• gnomAD v4: 3-128902825-CCT-C
• MyVariant Identifiers: chr3:g.128621669_128621670del (hg19) ; chr3:g.128902826_128902827del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128902828_128902829del , CM000665.2:g.128902828_128902829del	GRCh38
NC_000003.11:g.128621671_128621672del , CM000665.1:g.128621671_128621672del	GRCh37
NC_000003.10:g.130104361_130104362del	NCBI36
NG_017064.1:g.28339_28340del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.958+200_958+201del MANE Select	ENSP00000312618.7:n.958+200_958+201del
ENST00000511325.2:n.1036+200_1036+201del
ENST00000679399.1:c.*852+200_*852+201del	ENSP00000505434.1:n.*852+200_*852+201del
ENST00000679431.1:c.*834+196_*834+197del	ENSP00000506440.1:n.*834+196_*834+197del
ENST00000679613.1:c.958+200_958+201del	ENSP00000504971.1:n.958+200_958+201del
ENST00000679715.1:c.589+200_589+201del	ENSP00000506228.1:n.589+200_589+201del
ENST00000679824.1:c.*2264+200_*2264+201del	ENSP00000505516.1:n.*2264+200_*2264+201del
ENST00000679990.1:n.1193+200_1193+201del
ENST00000680636.1:c.958+200_958+201del	ENSP00000504886.1:n.958+200_958+201del
ENST00000680744.1:c.*311+200_*311+201del	ENSP00000505243.1:n.*311+200_*311+201del
ENST00000680764.1:c.*2362+196_*2362+197del	ENSP00000505126.1:n.*2362+196_*2362+197del
ENST00000681319.1:n.1036+200_1036+201del
ENST00000681367.1:c.958+200_958+201del	ENSP00000505309.1:n.958+200_958+201del
ENST00000681552.1:c.958+200_958+201del	ENSP00000505699.1:n.958+200_958+201del
ENST00000681583.1:c.958+200_958+201del	ENSP00000506340.1:n.958+200_958+201del
ENST00000681585.1:c.958+200_958+201del	ENSP00000506316.1:n.958+200_958+201del
ENST00000681589.1:n.1172+200_1172+201del
ENST00000681784.1:n.1036+200_1036+201del
ENST00000681886.1:c.*151+200_*151+201del	ENSP00000506500.1:n.*151+200_*151+201del
ENST00000308982.11:c.958+200_958+201del	ENSP00000312618.7:n.958+200_958+201del
ENST00000505192.5:c.*654+200_*654+201del	ENSP00000426277.1:n.*654+200_*654+201del
ENST00000505867.5:c.*758+200_*758+201del	ENSP00000425346.1:n.*758+200_*758+201del
ENST00000508971.1:c.247+200_247+201del	ENSP00000422683.1:n.247+200_247+201del
ENST00000511227.5:c.*852+200_*852+201del	ENSP00000425226.1:n.*852+200_*852+201del
ENST00000511526.5:n.463+196_463+197del
NM_014049.4:c.958+200_958+201del	NP_054768.2:n.958+200_958+201del
NR_033426.1:n.1336+200_1336+201del
XM_011512742.1:c.589+200_589+201del	XP_011511044.1:n.589+200_589+201del
XR_427367.1:n.1034+196_1034+197del
XM_024453484.1:c.589+200_589+201del	XP_024309252.1:n.589+200_589+201del
XM_024453485.1:c.589+200_589+201del	XP_024309253.1:n.589+200_589+201del
XR_427367.3:n.1034+196_1034+197del
NM_014049.5:c.958+200_958+201del MANE Select	NP_054768.2:n.958+200_958+201del
NR_033426.2:n.1206+200_1206+201del