Canonical Allele Identifier: CA1176721472

Gene: ACADM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75749535_75749538delinsAGCT , CM000663.2:g.75749535_75749538delinsAGCT	GRCh38
NC_000001.10:g.76215220_76215223delinsAGCT , CM000663.1:g.76215220_76215223delinsAGCT	GRCh37
NC_000001.9:g.75987808_75987811delinsAGCT	NCBI36
NG_007045.2:g.30178_30181delinsAGCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.825_828delinsAGCT MANE Select	ENSP00000359878.5:p.Gly275=
ENST00000473018.3:n.2949_2952delinsAGCT
ENST00000532207.6:n.1714_1717delinsAGCT
ENST00000541113.6:c.825_828delinsAGCT	ENSP00000442324.2:p.Gly275=
ENST00000679509.1:n.1787_1790delinsAGCT
ENST00000679530.1:c.*593_*596delinsAGCT	ENSP00000506454.1:n.*593_*596delinsAGCT
ENST00000679615.1:n.2840_2843delinsAGCT
ENST00000679687.1:c.387_390delinsAGCT	ENSP00000506598.1:p.Gly129=
ENST00000679704.1:c.*591_*594delinsAGCT	ENSP00000505117.1:n.*591_*594delinsAGCT
ENST00000679709.1:c.*788_*791delinsAGCT	ENSP00000506623.1:n.*788_*791delinsAGCT
ENST00000679976.1:c.*409_*412delinsAGCT	ENSP00000505565.1:n.*409_*412delinsAGCT
ENST00000680166.1:n.4114_4117delinsAGCT
ENST00000680517.1:c.*213_*216delinsAGCT	ENSP00000505803.1:n.*213_*216delinsAGCT
ENST00000680582.1:n.1787_1790delinsAGCT
ENST00000680613.1:c.*196_*199delinsAGCT	ENSP00000506114.1:n.*196_*199delinsAGCT
ENST00000680662.1:c.*739_*742delinsAGCT	ENSP00000505080.1:n.*739_*742delinsAGCT
ENST00000680691.1:c.*488_*491delinsAGCT	ENSP00000506487.1:n.*488_*491delinsAGCT
ENST00000680694.1:c.*413_*416delinsAGCT	ENSP00000505658.1:n.*413_*416delinsAGCT
ENST00000680743.1:c.*492_*495delinsAGCT	ENSP00000505073.1:n.*492_*495delinsAGCT
ENST00000680749.1:c.*110_*113delinsAGCT	ENSP00000505122.1:n.*110_*113delinsAGCT
ENST00000680798.1:c.*300_*303delinsAGCT	ENSP00000505670.1:n.*300_*303delinsAGCT
ENST00000680805.1:c.709-916_709-913delinsAGCT	ENSP00000505447.1:n.709-916_709-913delins...
ENST00000680844.1:c.*609_*612delinsAGCT	ENSP00000506541.1:n.*609_*612delinsAGCT
ENST00000680948.1:c.*692_*695delinsAGCT	ENSP00000505441.1:n.*692_*695delinsAGCT
ENST00000680964.1:c.825_828delinsAGCT	ENSP00000505961.1:p.Gly275=
ENST00000681037.1:c.*2309_*2312delinsAGCT	ENSP00000506025.1:n.*2309_*2312delinsAGCT...
ENST00000681063.1:c.600-916_600-913delinsAGCT	ENSP00000506616.1:n.600-916_600-913delins...
ENST00000681209.1:c.*480_*483delinsAGCT	ENSP00000505877.1:n.*480_*483delinsAGCT
ENST00000681278.1:n.1182_1185delinsAGCT
ENST00000681289.1:n.4820_4823delinsAGCT
ENST00000681361.1:c.*492_*495delinsAGCT	ENSP00000506679.1:n.*492_*495delinsAGCT
ENST00000681430.1:c.825_828delinsAGCT	ENSP00000506301.1:p.Gly275=
ENST00000681446.1:c.*407_*410delinsAGCT	ENSP00000506244.1:n.*407_*410delinsAGCT
ENST00000681450.1:c.*496_*499delinsAGCT	ENSP00000505660.1:n.*496_*499delinsAGCT
ENST00000681548.1:c.*411_*414delinsAGCT	ENSP00000505275.1:n.*411_*414delinsAGCT
ENST00000681616.1:c.*484_*487delinsAGCT	ENSP00000505111.1:n.*484_*487delinsAGCT
ENST00000681621.1:c.*409_*412delinsAGCT	ENSP00000505770.1:n.*409_*412delinsAGCT
ENST00000681680.1:n.2920_2923delinsAGCT
ENST00000681720.1:c.*280_*283delinsAGCT	ENSP00000505438.1:n.*280_*283delinsAGCT
ENST00000681730.1:n.1047_1050delinsAGCT
ENST00000681790.1:c.567_570delinsAGCT	ENSP00000505130.1:p.Gly189=
ENST00000681837.1:n.1441_1444delinsAGCT
ENST00000681913.1:n.2949_2952delinsAGCT
ENST00000681916.1:c.*593_*596delinsAGCT	ENSP00000506477.1:n.*593_*596delinsAGCT
ENST00000681930.1:n.2949_2952delinsAGCT
ENST00000370834.9:c.924_927delinsAGCT	ENSP00000359871.5:p.Gly308=
ENST00000370841.8:c.825_828delinsAGCT	ENSP00000359878.4:p.Gly275=
ENST00000420607.6:c.837_840delinsAGCT	ENSP00000409612.2:p.Gly279=
ENST00000525808.5:c.*411_*414delinsAGCT	ENSP00000434823.1:n.*411_*414delinsAGCT
ENST00000526129.5:c.*609_*612delinsAGCT	ENSP00000434092.1:n.*609_*612delinsAGCT
ENST00000526196.5:c.*593_*596delinsAGCT	ENSP00000431953.1:n.*593_*596delinsAGCT
ENST00000528016.1:c.39_42delinsAGCT	ENSP00000434284.1:p.Gly13=
ENST00000529059.5:n.734_737delinsAGCT
ENST00000530953.6:c.*322_*325delinsAGCT	ENSP00000431372.1:n.*322_*325delinsAGCT
ENST00000532207.5:n.555_558delinsAGCT
ENST00000532509.5:c.*589_*592delinsAGCT	ENSP00000432522.1:n.*589_*592delinsAGCT
ENST00000534334.5:c.*409_*412delinsAGCT	ENSP00000435584.1:n.*409_*412delinsAGCT
ENST00000541113.5:c.717_720delinsAGCT	ENSP00000442324.1:p.Gly239=
NM_000016.5:c.825_828delinsAGCT	NP_000007.1:p.Gly275=
NM_001127328.2:c.837_840delinsAGCT	NP_001120800.1:p.Gly279=
NM_001286042.1:c.717_720delinsAGCT	NP_001272971.1:p.Gly239=
NM_001286043.1:c.924_927delinsAGCT	NP_001272972.1:p.Gly308=
NM_001286044.1:c.258_261delinsAGCT	NP_001272973.1:p.Gly86=
NM_000016.6:c.825_828delinsAGCT MANE Select	NP_000007.1:p.Gly275=
NM_001127328.3:c.837_840delinsAGCT	NP_001120800.1:p.Gly279=
NM_001286042.2:c.717_720delinsAGCT	NP_001272971.1:p.Gly239=
NM_001286043.2:c.924_927delinsAGCT	NP_001272972.1:p.Gly308=
NM_001286044.2:c.258_261delinsAGCT	NP_001272973.1:p.Gly86=