Canonical Allele Identifier: CA2739291979

Gene: ACADM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75749502del , CM000663.2:g.75749502del	GRCh38
NC_000001.10:g.76215187del , CM000663.1:g.76215187del	GRCh37
NC_000001.9:g.75987775del	NCBI36
NG_007045.2:g.30145del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.792del MANE Select	ENSP00000359878.5:p.Ile264MetfsTer20
ENST00000473018.3:n.2916del
ENST00000532207.6:n.1681del
ENST00000541113.6:c.792del	ENSP00000442324.2:p.Ile264MetfsTer?
ENST00000679509.1:n.1754del
ENST00000679530.1:c.*560del	ENSP00000506454.1:n.*560del
ENST00000679615.1:n.2807del
ENST00000679687.1:c.354del	ENSP00000506598.1:p.Ile118MetfsTer20
ENST00000679704.1:c.*558del	ENSP00000505117.1:n.*558del
ENST00000679709.1:c.*755del	ENSP00000506623.1:n.*755del
ENST00000679976.1:c.*376del	ENSP00000505565.1:n.*376del
ENST00000680166.1:n.4081del
ENST00000680517.1:c.*180del	ENSP00000505803.1:n.*180del
ENST00000680582.1:n.1754del
ENST00000680613.1:c.*163del	ENSP00000506114.1:n.*163del
ENST00000680662.1:c.*706del	ENSP00000505080.1:n.*706del
ENST00000680691.1:c.*455del	ENSP00000506487.1:n.*455del
ENST00000680694.1:c.*380del	ENSP00000505658.1:n.*380del
ENST00000680743.1:c.*459del	ENSP00000505073.1:n.*459del
ENST00000680749.1:c.*77del	ENSP00000505122.1:n.*77del
ENST00000680798.1:c.*267del	ENSP00000505670.1:n.*267del
ENST00000680805.1:c.709-949del	ENSP00000505447.1:n.709-949del
ENST00000680844.1:c.*576del	ENSP00000506541.1:n.*576del
ENST00000680948.1:c.*659del	ENSP00000505441.1:n.*659del
ENST00000680964.1:c.792del	ENSP00000505961.1:p.Ile264MetfsTer20
ENST00000681037.1:c.*2276del	ENSP00000506025.1:n.*2276del
ENST00000681063.1:c.600-949del	ENSP00000506616.1:n.600-949del
ENST00000681209.1:c.*447del	ENSP00000505877.1:n.*447del
ENST00000681278.1:n.1149del
ENST00000681289.1:n.4787del
ENST00000681361.1:c.*459del	ENSP00000506679.1:n.*459del
ENST00000681430.1:c.792del	ENSP00000506301.1:p.Ile264MetfsTer20
ENST00000681446.1:c.*374del	ENSP00000506244.1:n.*374del
ENST00000681450.1:c.*463del	ENSP00000505660.1:n.*463del
ENST00000681548.1:c.*378del	ENSP00000505275.1:n.*378del
ENST00000681616.1:c.*451del	ENSP00000505111.1:n.*451del
ENST00000681621.1:c.*376del	ENSP00000505770.1:n.*376del
ENST00000681680.1:n.2887del
ENST00000681720.1:c.*247del	ENSP00000505438.1:n.*247del
ENST00000681730.1:n.1014del
ENST00000681790.1:c.534del	ENSP00000505130.1:p.Ile178MetfsTer20
ENST00000681837.1:n.1408del
ENST00000681913.1:n.2916del
ENST00000681916.1:c.*560del	ENSP00000506477.1:n.*560del
ENST00000681930.1:n.2916del
ENST00000370834.9:c.891del	ENSP00000359871.5:p.Ile297MetfsTer20
ENST00000370841.8:c.792del	ENSP00000359878.4:p.Ile264MetfsTer20
ENST00000420607.6:c.804del	ENSP00000409612.2:p.Ile268MetfsTer20
ENST00000525808.5:c.*378del	ENSP00000434823.1:n.*378del
ENST00000526129.5:c.*576del	ENSP00000434092.1:n.*576del
ENST00000526196.5:c.*560del	ENSP00000431953.1:n.*560del
ENST00000526930.1:n.565del
ENST00000528016.1:c.6del	ENSP00000434284.1:p.Ile2MetfsTer20
ENST00000529059.5:n.701del
ENST00000530953.6:c.*289del	ENSP00000431372.1:n.*289del
ENST00000532207.5:n.522del
ENST00000532509.5:c.*556del	ENSP00000432522.1:n.*556del
ENST00000534334.5:c.*376del	ENSP00000435584.1:n.*376del
ENST00000541113.5:c.684del	ENSP00000442324.1:p.Ile228MetfsTer20
NM_000016.5:c.792del	NP_000007.1:p.Ile264MetfsTer20
NM_001127328.2:c.804del	NP_001120800.1:p.Ile268MetfsTer20
NM_001286042.1:c.684del	NP_001272971.1:p.Ile228MetfsTer20
NM_001286043.1:c.891del	NP_001272972.1:p.Ile297MetfsTer20
NM_001286044.1:c.225del	NP_001272973.1:p.Ile75MetfsTer20
NM_000016.6:c.792del MANE Select	NP_000007.1:p.Ile264MetfsTer20
NM_001127328.3:c.804del	NP_001120800.1:p.Ile268MetfsTer20
NM_001286042.2:c.684del	NP_001272971.1:p.Ile228MetfsTer20
NM_001286043.2:c.891del	NP_001272972.1:p.Ile297MetfsTer20
NM_001286044.2:c.225del	NP_001272973.1:p.Ile75MetfsTer20