Canonical Allele Identifier: CA2667560281

Gene: ACAD9

Linked Data

• gnomAD v4: 3-128904231-GGAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128904237_128904239del , CM000665.2:g.128904237_128904239del	GRCh38
NC_000003.11:g.128623080_128623082del , CM000665.1:g.128623080_128623082del	GRCh37
NC_000003.10:g.130105770_130105772del	NCBI36
NG_017064.1:g.29748_29750del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1029+105_1029+107del MANE Select	ENSP00000312618.7:n.1029+105_1029+107del
ENST00000511325.2:n.1107+105_1107+107del
ENST00000679399.1:c.*923+105_*923+107del	ENSP00000505434.1:n.*923+105_*923+107del
ENST00000679431.1:c.*905+105_*905+107del	ENSP00000506440.1:n.*905+105_*905+107del
ENST00000679613.1:c.1029+105_1029+107del	ENSP00000504971.1:n.1029+105_1029+107del
ENST00000679715.1:c.660+105_660+107del	ENSP00000506228.1:n.660+105_660+107del
ENST00000679824.1:c.*2335+105_*2335+107del	ENSP00000505516.1:n.*2335+105_*2335+107del
ENST00000679990.1:n.1264+105_1264+107del
ENST00000680636.1:c.1029+105_1029+107del	ENSP00000504886.1:n.1029+105_1029+107del
ENST00000680744.1:c.*382+105_*382+107del	ENSP00000505243.1:n.*382+105_*382+107del
ENST00000680764.1:c.*2433+105_*2433+107del	ENSP00000505126.1:n.*2433+105_*2433+107del
ENST00000681319.1:n.1107+105_1107+107del
ENST00000681367.1:c.1029+105_1029+107del	ENSP00000505309.1:n.1029+105_1029+107del
ENST00000681552.1:c.1029+105_1029+107del	ENSP00000505699.1:n.1029+105_1029+107del
ENST00000681583.1:c.1029+105_1029+107del	ENSP00000506340.1:n.1029+105_1029+107del
ENST00000681585.1:c.1029+105_1029+107del	ENSP00000506316.1:n.1029+105_1029+107del
ENST00000681589.1:n.1243+105_1243+107del
ENST00000681784.1:n.1107+105_1107+107del
ENST00000681886.1:c.*222+105_*222+107del	ENSP00000506500.1:n.*222+105_*222+107del
ENST00000308982.11:c.1029+105_1029+107del	ENSP00000312618.7:n.1029+105_1029+107del
ENST00000505192.5:c.*725+105_*725+107del	ENSP00000426277.1:n.*725+105_*725+107del
ENST00000505867.5:c.*829+105_*829+107del	ENSP00000425346.1:n.*829+105_*829+107del
ENST00000508971.1:c.318+105_318+107del	ENSP00000422683.1:n.318+105_318+107del
ENST00000511227.5:c.*923+105_*923+107del	ENSP00000425226.1:n.*923+105_*923+107del
ENST00000511526.5:n.534+105_534+107del
NM_014049.4:c.1029+105_1029+107del	NP_054768.2:n.1029+105_1029+107del
NR_033426.1:n.1407+105_1407+107del
XM_011512742.1:c.660+105_660+107del	XP_011511044.1:n.660+105_660+107del
XR_427367.1:n.1105+105_1105+107del
XM_024453484.1:c.660+105_660+107del	XP_024309252.1:n.660+105_660+107del
XM_024453485.1:c.660+105_660+107del	XP_024309253.1:n.660+105_660+107del
XR_427367.3:n.1105+105_1105+107del
NM_014049.5:c.1029+105_1029+107del MANE Select	NP_054768.2:n.1029+105_1029+107del
NR_033426.2:n.1277+105_1277+107del