Canonical Allele Identifier: CA2646248338

Gene: ACADM

Linked Data

• gnomAD v4: 1-75734852-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75734853_75734854del , CM000663.2:g.75734853_75734854del	GRCh38
NC_000001.10:g.76200538_76200539del , CM000663.1:g.76200538_76200539del	GRCh37
NC_000001.9:g.75973126_75973127del	NCBI36
NG_007045.2:g.15496_15497del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.450_451del MANE Select	ENSP00000359878.5:p.Glu151GlyfsTer17
ENST00000473018.3:n.2574_2575del
ENST00000525881.6:n.1412_1413del
ENST00000541113.6:c.450_451del	ENSP00000442324.2:p.Glu151GlyfsTer17
ENST00000679509.1:n.1412_1413del
ENST00000679530.1:c.*218_*219del	ENSP00000506454.1:n.*218_*219del
ENST00000679615.1:n.2574_2575del
ENST00000679687.1:c.31-5127_31-5126del	ENSP00000506598.1:n.31-5127_31-5126del
ENST00000679704.1:c.*216_*217del	ENSP00000505117.1:n.*216_*217del
ENST00000679709.1:c.*413_*414del	ENSP00000506623.1:n.*413_*414del
ENST00000679804.1:n.207+1931_207+1932del
ENST00000679976.1:c.*34_*35del	ENSP00000505565.1:n.*34_*35del
ENST00000680166.1:n.3739_3740del
ENST00000680517.1:c.286+1931_286+1932del	ENSP00000505803.1:n.286+1931_286+1932del
ENST00000680582.1:n.1412_1413del
ENST00000680613.1:c.450_451del	ENSP00000506114.1:p.Glu151GlyfsTer17
ENST00000680662.1:c.*364_*365del	ENSP00000505080.1:n.*364_*365del
ENST00000680691.1:c.*113_*114del	ENSP00000506487.1:n.*113_*114del
ENST00000680694.1:c.*34_*35del	ENSP00000505658.1:n.*34_*35del
ENST00000680743.1:c.*117_*118del	ENSP00000505073.1:n.*117_*118del
ENST00000680749.1:c.450_451del	ENSP00000505122.1:p.Glu151GlyfsTer17
ENST00000680798.1:c.*34_*35del	ENSP00000505670.1:n.*34_*35del
ENST00000680805.1:c.450_451del	ENSP00000505447.1:p.Glu151GlyfsTer17
ENST00000680844.1:c.*234_*235del	ENSP00000506541.1:n.*234_*235del
ENST00000680948.1:c.*317_*318del	ENSP00000505441.1:n.*317_*318del
ENST00000680964.1:c.450_451del	ENSP00000505961.1:p.Glu151GlyfsTer17
ENST00000681037.1:c.450_451del	ENSP00000506025.1:p.Glu151GlyfsTer17
ENST00000681063.1:c.450_451del	ENSP00000506616.1:p.Glu151GlyfsTer17
ENST00000681209.1:c.*214_*215del	ENSP00000505877.1:n.*214_*215del
ENST00000681278.1:n.807_808del
ENST00000681289.1:n.807_808del
ENST00000681361.1:c.*117_*118del	ENSP00000506679.1:n.*117_*118del
ENST00000681430.1:c.450_451del	ENSP00000506301.1:p.Glu151GlyfsTer17
ENST00000681446.1:c.*34_*35del	ENSP00000506244.1:n.*34_*35del
ENST00000681450.1:c.*117_*118del	ENSP00000505660.1:n.*117_*118del
ENST00000681548.1:c.*54+1931_*54+1932del	ENSP00000505275.1:n.*54+1931_*54+1932del
ENST00000681616.1:c.*218_*219del	ENSP00000505111.1:n.*218_*219del
ENST00000681621.1:c.*34_*35del	ENSP00000505770.1:n.*34_*35del
ENST00000681680.1:n.2574_2575del
ENST00000681720.1:c.*54+1931_*54+1932del	ENSP00000505438.1:n.*54+1931_*54+1932del
ENST00000681730.1:n.672_673del
ENST00000681790.1:c.192_193del	ENSP00000505130.1:p.Glu65GlyfsTer17
ENST00000681837.1:n.1066_1067del
ENST00000681913.1:n.2574_2575del
ENST00000681916.1:c.*218_*219del	ENSP00000506477.1:n.*218_*219del
ENST00000681930.1:n.2574_2575del
ENST00000370834.9:c.549_550del	ENSP00000359871.5:p.Glu184GlyfsTer17
ENST00000370841.8:c.450_451del	ENSP00000359878.4:p.Glu151GlyfsTer17
ENST00000420607.6:c.462_463del	ENSP00000409612.2:p.Glu155GlyfsTer17
ENST00000525808.5:c.*54+1931_*54+1932del	ENSP00000434823.1:n.*54+1931_*54+1932del
ENST00000526129.5:c.*234_*235del	ENSP00000434092.1:n.*234_*235del
ENST00000526196.5:c.*218_*219del	ENSP00000431953.1:n.*218_*219del
ENST00000526930.1:n.223_224del
ENST00000529059.5:n.359_360del
ENST00000530953.6:c.119-5127_119-5126del	ENSP00000431372.1:n.119-5127_119-5126del
ENST00000532509.5:c.*214_*215del	ENSP00000432522.1:n.*214_*215del
ENST00000534334.5:c.*34_*35del	ENSP00000435584.1:n.*34_*35del
ENST00000541113.5:c.342_343del	ENSP00000442324.1:p.Glu115GlyfsTer17
NM_000016.5:c.450_451del	NP_000007.1:p.Glu151GlyfsTer17
NM_001127328.2:c.462_463del	NP_001120800.1:p.Glu155GlyfsTer17
NM_001286042.1:c.342_343del	NP_001272971.1:p.Glu115GlyfsTer17
NM_001286043.1:c.549_550del	NP_001272972.1:p.Glu184GlyfsTer17
NM_001286044.1:c.-100+1931_-100+1932del	NP_001272973.1:n.-100+1931_-100+1932del
NM_000016.6:c.450_451del MANE Select	NP_000007.1:p.Glu151GlyfsTer17
NM_001127328.3:c.462_463del	NP_001120800.1:p.Glu155GlyfsTer17
NM_001286042.2:c.342_343del	NP_001272971.1:p.Glu115GlyfsTer17
NM_001286043.2:c.549_550del	NP_001272972.1:p.Glu184GlyfsTer17
NM_001286044.2:c.-100+1931_-100+1932del	NP_001272973.1:n.-100+1931_-100+1932del