Canonical Allele Identifier: CA1176726830
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761198C= , CM000663.2:g.75761198C= GRCh38
NC_000001.10:g.76226883C= , CM000663.1:g.76226883C= GRCh37
NC_000001.9:g.75999471C= NCBI36
NG_007045.2:g.41841C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1022C= MANE Select ENSP00000359878.5:p.Ala341=
ENST00000473018.3:n.3146C=
ENST00000532207.6:n.2033C=
ENST00000541113.6:c.926C= ENSP00000442324.2:p.Ala309=
ENST00000679509.1:n.1984C=
ENST00000679530.1:c.*790C= ENSP00000506454.1:n.*790C=
ENST00000679615.1:n.3037C=
ENST00000679687.1:c.584C= ENSP00000506598.1:p.Ala195=
ENST00000679704.1:c.*788C= ENSP00000505117.1:n.*788C=
ENST00000679709.1:c.*985C= ENSP00000506623.1:n.*985C=
ENST00000679976.1:c.*606C= ENSP00000505565.1:n.*606C=
ENST00000680166.1:n.4311C=
ENST00000680315.1:n.905C=
ENST00000680517.1:c.*410C= ENSP00000505803.1:n.*410C=
ENST00000680582.1:n.1984C=
ENST00000680613.1:c.*515C= ENSP00000506114.1:n.*515C=
ENST00000680662.1:c.*936C= ENSP00000505080.1:n.*936C=
ENST00000680691.1:c.*685C= ENSP00000506487.1:n.*685C=
ENST00000680694.1:c.*610C= ENSP00000505658.1:n.*610C=
ENST00000680743.1:c.*811C= ENSP00000505073.1:n.*811C=
ENST00000680749.1:c.*307C= ENSP00000505122.1:n.*307C=
ENST00000680798.1:c.*497C= ENSP00000505670.1:n.*497C=
ENST00000680805.1:c.881C= ENSP00000505447.1:p.Ala294=
ENST00000680844.1:c.*806C= ENSP00000506541.1:n.*806C=
ENST00000680948.1:c.*889C= ENSP00000505441.1:n.*889C=
ENST00000680964.1:c.*115C= ENSP00000505961.1:n.*115C=
ENST00000681037.1:c.*2506C= ENSP00000506025.1:n.*2506C=
ENST00000681063.1:c.*291C= ENSP00000506616.1:n.*291C=
ENST00000681209.1:c.*677C= ENSP00000505877.1:n.*677C=
ENST00000681278.1:n.1724C=
ENST00000681289.1:n.5017C=
ENST00000681361.1:c.*689C= ENSP00000506679.1:n.*689C=
ENST00000681430.1:c.*115C= ENSP00000506301.1:n.*115C=
ENST00000681446.1:c.*726C= ENSP00000506244.1:n.*726C=
ENST00000681450.1:c.*693C= ENSP00000505660.1:n.*693C=
ENST00000681548.1:c.*608C= ENSP00000505275.1:n.*608C=
ENST00000681616.1:c.*681C= ENSP00000505111.1:n.*681C=
ENST00000681621.1:c.*606C= ENSP00000505770.1:n.*606C=
ENST00000681680.1:n.3117C=
ENST00000681720.1:c.*477C= ENSP00000505438.1:n.*477C=
ENST00000681730.1:n.1244C=
ENST00000681790.1:c.764C= ENSP00000505130.1:p.Ala255=
ENST00000681837.1:n.1638C=
ENST00000681913.1:n.3268C=
ENST00000681916.1:c.*790C= ENSP00000506477.1:n.*790C=
ENST00000681930.1:n.3146C=
ENST00000370834.9:c.1121C= ENSP00000359871.5:p.Ala374=
ENST00000370841.8:c.1022C= ENSP00000359878.4:p.Ala341=
ENST00000420607.6:c.1034C= ENSP00000409612.2:p.Ala345=
ENST00000481374.1:n.295C=
ENST00000525808.5:c.*608C= ENSP00000434823.1:n.*608C=
ENST00000526129.5:c.*806C= ENSP00000434092.1:n.*806C=
ENST00000526196.5:c.*790C= ENSP00000431953.1:n.*790C=
ENST00000528016.1:c.160-7979C= ENSP00000434284.1:n.160-7979C=
ENST00000529059.5:n.931C=
ENST00000532207.5:n.752C=
ENST00000534334.5:c.*763C= ENSP00000435584.1:n.*763C=
ENST00000541113.5:c.914C= ENSP00000442324.1:p.Ala305=
NM_000016.5:c.1022C= NP_000007.1:p.Ala341=
NM_001127328.2:c.1034C= NP_001120800.1:p.Ala345=
NM_001286042.1:c.914C= NP_001272971.1:p.Ala305=
NM_001286043.1:c.1121C= NP_001272972.1:p.Ala374=
NM_001286044.1:c.455C= NP_001272973.1:p.Ala152=
NM_000016.6:c.1022C= MANE Select NP_000007.1:p.Ala341=
NM_001127328.3:c.1034C= NP_001120800.1:p.Ala345=
NM_001286042.2:c.914C= NP_001272971.1:p.Ala305=
NM_001286043.2:c.1121C= NP_001272972.1:p.Ala374=
NM_001286044.2:c.455C= NP_001272973.1:p.Ala152=