Canonical Allele Identifier: CA1400924382

Gene: ACAD9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128904179_128904180delinsGA , CM000665.2:g.128904179_128904180delinsGA	GRCh38
NC_000003.11:g.128623022_128623023delinsGA , CM000665.1:g.128623022_128623023delinsGA	GRCh37
NC_000003.10:g.130105712_130105713delinsGA	NCBI36
NG_017064.1:g.29690_29691delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308982.12:c.1029+47_1029+48delinsGA MANE Select	ENSP00000312618.7:n.1029+47_1029+48delinsGA
ENST00000511325.2:n.1107+47_1107+48delinsGA
ENST00000679399.1:c.*923+47_*923+48delinsGA	ENSP00000505434.1:n.*923+47_*923+48delinsGA
ENST00000679431.1:c.*905+47_*905+48delinsGA	ENSP00000506440.1:n.*905+47_*905+48delinsGA
ENST00000679613.1:c.1029+47_1029+48delinsGA	ENSP00000504971.1:n.1029+47_1029+48delinsGA
ENST00000679715.1:c.660+47_660+48delinsGA	ENSP00000506228.1:n.660+47_660+48delinsGA
ENST00000679824.1:c.*2335+47_*2335+48delinsGA	ENSP00000505516.1:n.*2335+47_*2335+48delinsGA
ENST00000679990.1:n.1264+47_1264+48delinsGA
ENST00000680636.1:c.1029+47_1029+48delinsGA	ENSP00000504886.1:n.1029+47_1029+48delinsGA
ENST00000680744.1:c.*382+47_*382+48delinsGA	ENSP00000505243.1:n.*382+47_*382+48delinsGA
ENST00000680764.1:c.*2433+47_*2433+48delinsGA	ENSP00000505126.1:n.*2433+47_*2433+48delinsGA
ENST00000681319.1:n.1107+47_1107+48delinsGA
ENST00000681367.1:c.1029+47_1029+48delinsGA	ENSP00000505309.1:n.1029+47_1029+48delinsGA
ENST00000681552.1:c.1029+47_1029+48delinsGA	ENSP00000505699.1:n.1029+47_1029+48delinsGA
ENST00000681583.1:c.1029+47_1029+48delinsGA	ENSP00000506340.1:n.1029+47_1029+48delinsGA
ENST00000681585.1:c.1029+47_1029+48delinsGA	ENSP00000506316.1:n.1029+47_1029+48delinsGA
ENST00000681589.1:n.1243+47_1243+48delinsGA
ENST00000681784.1:n.1107+47_1107+48delinsGA
ENST00000681886.1:c.*222+47_*222+48delinsGA	ENSP00000506500.1:n.*222+47_*222+48delinsGA
ENST00000308982.11:c.1029+47_1029+48delinsGA	ENSP00000312618.7:n.1029+47_1029+48delinsGA
ENST00000505192.5:c.*725+47_*725+48delinsGA	ENSP00000426277.1:n.*725+47_*725+48delinsGA
ENST00000505867.5:c.*829+47_*829+48delinsGA	ENSP00000425346.1:n.*829+47_*829+48delinsGA
ENST00000508971.1:c.318+47_318+48delinsGA	ENSP00000422683.1:n.318+47_318+48delinsGA
ENST00000511227.5:c.*923+47_*923+48delinsGA	ENSP00000425226.1:n.*923+47_*923+48delinsGA
ENST00000511526.5:n.534+47_534+48delinsGA
NM_014049.4:c.1029+47_1029+48delinsGA	NP_054768.2:n.1029+47_1029+48delinsGA
NR_033426.1:n.1407+47_1407+48delinsGA
XM_011512742.1:c.660+47_660+48delinsGA	XP_011511044.1:n.660+47_660+48delinsGA
XR_427367.1:n.1105+47_1105+48delinsGA
XM_024453484.1:c.660+47_660+48delinsGA	XP_024309252.1:n.660+47_660+48delinsGA
XM_024453485.1:c.660+47_660+48delinsGA	XP_024309253.1:n.660+47_660+48delinsGA
XR_427367.3:n.1105+47_1105+48delinsGA
NM_014049.5:c.1029+47_1029+48delinsGA MANE Select	NP_054768.2:n.1029+47_1029+48delinsGA
NR_033426.2:n.1277+47_1277+48delinsGA