Canonical Allele Identifier: CA1176726884

Gene: ACADM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761344_75761346delinsCTA , CM000663.2:g.75761344_75761346delinsCTA	GRCh38
NC_000001.10:g.76227029_76227031delinsCTA , CM000663.1:g.76227029_76227031delinsCTA	GRCh37
NC_000001.9:g.75999617_75999619delinsCTA	NCBI36
NG_007045.2:g.41987_41989delinsCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.1168_1170delinsCTA MANE Select	ENSP00000359878.5:p.Leu390=
ENST00000473018.3:n.3292_3294delinsCTA
ENST00000532207.6:n.2179_2181delinsCTA
ENST00000541113.6:c.1072_1074delinsCTA	ENSP00000442324.2:p.Leu358=
ENST00000679509.1:n.2130_2132delinsCTA
ENST00000679530.1:c.*936_*938delinsCTA	ENSP00000506454.1:n.*936_*938delinsCTA
ENST00000679615.1:n.3183_3185delinsCTA
ENST00000679687.1:c.730_732delinsCTA	ENSP00000506598.1:p.Leu244=
ENST00000679704.1:c.*934_*936delinsCTA	ENSP00000505117.1:n.*934_*936delinsCTA
ENST00000679709.1:c.*1131_*1133delinsCTA	ENSP00000506623.1:n.*1131_*1133delinsCTA
ENST00000679976.1:c.*752_*754delinsCTA	ENSP00000505565.1:n.*752_*754delinsCTA
ENST00000680166.1:n.4457_4459delinsCTA
ENST00000680315.1:n.1051_1053delinsCTA
ENST00000680517.1:c.*556_*558delinsCTA	ENSP00000505803.1:n.*556_*558delinsCTA
ENST00000680582.1:n.2130_2132delinsCTA
ENST00000680613.1:c.*661_*663delinsCTA	ENSP00000506114.1:n.*661_*663delinsCTA
ENST00000680662.1:c.*1082_*1084delinsCTA	ENSP00000505080.1:n.*1082_*1084delinsCTA
ENST00000680691.1:c.*831_*833delinsCTA	ENSP00000506487.1:n.*831_*833delinsCTA
ENST00000680694.1:c.*756_*758delinsCTA	ENSP00000505658.1:n.*756_*758delinsCTA
ENST00000680743.1:c.*957_*959delinsCTA	ENSP00000505073.1:n.*957_*959delinsCTA
ENST00000680749.1:c.*453_*455delinsCTA	ENSP00000505122.1:n.*453_*455delinsCTA
ENST00000680798.1:c.*643_*645delinsCTA	ENSP00000505670.1:n.*643_*645delinsCTA
ENST00000680805.1:c.1027_1029delinsCTA	ENSP00000505447.1:p.Leu343=
ENST00000680844.1:c.*952_*954delinsCTA	ENSP00000506541.1:n.*952_*954delinsCTA
ENST00000680948.1:c.*1035_*1037delinsCTA	ENSP00000505441.1:n.*1035_*1037delinsCTA
ENST00000680964.1:c.*261_*263delinsCTA	ENSP00000505961.1:n.*261_*263delinsCTA
ENST00000681037.1:c.*2652_*2654delinsCTA	ENSP00000506025.1:n.*2652_*2654delinsCTA
ENST00000681063.1:c.*437_*439delinsCTA	ENSP00000506616.1:n.*437_*439delinsCTA
ENST00000681209.1:c.*823_*825delinsCTA	ENSP00000505877.1:n.*823_*825delinsCTA
ENST00000681278.1:n.1870_1872delinsCTA
ENST00000681289.1:n.5163_5165delinsCTA
ENST00000681361.1:c.*835_*837delinsCTA	ENSP00000506679.1:n.*835_*837delinsCTA
ENST00000681430.1:c.*261_*263delinsCTA	ENSP00000506301.1:n.*261_*263delinsCTA
ENST00000681446.1:c.*872_*874delinsCTA	ENSP00000506244.1:n.*872_*874delinsCTA
ENST00000681450.1:c.*839_*841delinsCTA	ENSP00000505660.1:n.*839_*841delinsCTA
ENST00000681548.1:c.*754_*756delinsCTA	ENSP00000505275.1:n.*754_*756delinsCTA
ENST00000681616.1:c.*827_*829delinsCTA	ENSP00000505111.1:n.*827_*829delinsCTA
ENST00000681621.1:c.*752_*754delinsCTA	ENSP00000505770.1:n.*752_*754delinsCTA
ENST00000681680.1:n.3263_3265delinsCTA
ENST00000681720.1:c.*623_*625delinsCTA	ENSP00000505438.1:n.*623_*625delinsCTA
ENST00000681730.1:n.1390_1392delinsCTA
ENST00000681790.1:c.910_912delinsCTA	ENSP00000505130.1:p.Leu304=
ENST00000681837.1:n.1784_1786delinsCTA
ENST00000681913.1:n.3414_3416delinsCTA
ENST00000681916.1:c.*936_*938delinsCTA	ENSP00000506477.1:n.*936_*938delinsCTA
ENST00000681930.1:n.3292_3294delinsCTA
ENST00000370834.9:c.1267_1269delinsCTA	ENSP00000359871.5:p.Leu423=
ENST00000370841.8:c.1168_1170delinsCTA	ENSP00000359878.4:p.Leu390=
ENST00000420607.6:c.1180_1182delinsCTA	ENSP00000409612.2:p.Leu394=
ENST00000481374.1:n.441_443delinsCTA
ENST00000525808.5:c.*754_*756delinsCTA	ENSP00000434823.1:n.*754_*756delinsCTA
ENST00000526129.5:c.*952_*954delinsCTA	ENSP00000434092.1:n.*952_*954delinsCTA
ENST00000526196.5:c.*936_*938delinsCTA	ENSP00000431953.1:n.*936_*938delinsCTA
ENST00000528016.1:c.160-7833_160-7831delinsCTA	ENSP00000434284.1:n.160-7833_160-7831delinsCTA
ENST00000529059.5:n.1077_1079delinsCTA
ENST00000541113.5:c.1060_1062delinsCTA	ENSP00000442324.1:p.Leu354=
NM_000016.5:c.1168_1170delinsCTA	NP_000007.1:p.Leu390=
NM_001127328.2:c.1180_1182delinsCTA	NP_001120800.1:p.Leu394=
NM_001286042.1:c.1060_1062delinsCTA	NP_001272971.1:p.Leu354=
NM_001286043.1:c.1267_1269delinsCTA	NP_001272972.1:p.Leu423=
NM_001286044.1:c.601_603delinsCTA	NP_001272973.1:p.Leu201=
NM_000016.6:c.1168_1170delinsCTA MANE Select	NP_000007.1:p.Leu390=
NM_001127328.3:c.1180_1182delinsCTA	NP_001120800.1:p.Leu394=
NM_001286042.2:c.1060_1062delinsCTA	NP_001272971.1:p.Leu354=
NM_001286043.2:c.1267_1269delinsCTA	NP_001272972.1:p.Leu423=
NM_001286044.2:c.601_603delinsCTA	NP_001272973.1:p.Leu201=