Canonical Allele Identifier: CA1176726866
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761289T= , CM000663.2:g.75761289T= GRCh38
NC_000001.10:g.76226974T= , CM000663.1:g.76226974T= GRCh37
NC_000001.9:g.75999562T= NCBI36
NG_007045.2:g.41932T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1113T= MANE Select ENSP00000359878.5:p.Asp371=
ENST00000473018.3:n.3237T=
ENST00000532207.6:n.2124T=
ENST00000541113.6:c.1017T= ENSP00000442324.2:p.Asp339=
ENST00000679509.1:n.2075T=
ENST00000679530.1:c.*881T= ENSP00000506454.1:n.*881T=
ENST00000679615.1:n.3128T=
ENST00000679687.1:c.675T= ENSP00000506598.1:p.Asp225=
ENST00000679704.1:c.*879T= ENSP00000505117.1:n.*879T=
ENST00000679709.1:c.*1076T= ENSP00000506623.1:n.*1076T=
ENST00000679976.1:c.*697T= ENSP00000505565.1:n.*697T=
ENST00000680166.1:n.4402T=
ENST00000680315.1:n.996T=
ENST00000680517.1:c.*501T= ENSP00000505803.1:n.*501T=
ENST00000680582.1:n.2075T=
ENST00000680613.1:c.*606T= ENSP00000506114.1:n.*606T=
ENST00000680662.1:c.*1027T= ENSP00000505080.1:n.*1027T=
ENST00000680691.1:c.*776T= ENSP00000506487.1:n.*776T=
ENST00000680694.1:c.*701T= ENSP00000505658.1:n.*701T=
ENST00000680743.1:c.*902T= ENSP00000505073.1:n.*902T=
ENST00000680749.1:c.*398T= ENSP00000505122.1:n.*398T=
ENST00000680798.1:c.*588T= ENSP00000505670.1:n.*588T=
ENST00000680805.1:c.972T= ENSP00000505447.1:p.Asp324=
ENST00000680844.1:c.*897T= ENSP00000506541.1:n.*897T=
ENST00000680948.1:c.*980T= ENSP00000505441.1:n.*980T=
ENST00000680964.1:c.*206T= ENSP00000505961.1:n.*206T=
ENST00000681037.1:c.*2597T= ENSP00000506025.1:n.*2597T=
ENST00000681063.1:c.*382T= ENSP00000506616.1:n.*382T=
ENST00000681209.1:c.*768T= ENSP00000505877.1:n.*768T=
ENST00000681278.1:n.1815T=
ENST00000681289.1:n.5108T=
ENST00000681361.1:c.*780T= ENSP00000506679.1:n.*780T=
ENST00000681430.1:c.*206T= ENSP00000506301.1:n.*206T=
ENST00000681446.1:c.*817T= ENSP00000506244.1:n.*817T=
ENST00000681450.1:c.*784T= ENSP00000505660.1:n.*784T=
ENST00000681548.1:c.*699T= ENSP00000505275.1:n.*699T=
ENST00000681616.1:c.*772T= ENSP00000505111.1:n.*772T=
ENST00000681621.1:c.*697T= ENSP00000505770.1:n.*697T=
ENST00000681680.1:n.3208T=
ENST00000681720.1:c.*568T= ENSP00000505438.1:n.*568T=
ENST00000681730.1:n.1335T=
ENST00000681790.1:c.855T= ENSP00000505130.1:p.Asp285=
ENST00000681837.1:n.1729T=
ENST00000681913.1:n.3359T=
ENST00000681916.1:c.*881T= ENSP00000506477.1:n.*881T=
ENST00000681930.1:n.3237T=
ENST00000370834.9:c.1212T= ENSP00000359871.5:p.Asp404=
ENST00000370841.8:c.1113T= ENSP00000359878.4:p.Asp371=
ENST00000420607.6:c.1125T= ENSP00000409612.2:p.Asp375=
ENST00000481374.1:n.386T=
ENST00000525808.5:c.*699T= ENSP00000434823.1:n.*699T=
ENST00000526129.5:c.*897T= ENSP00000434092.1:n.*897T=
ENST00000526196.5:c.*881T= ENSP00000431953.1:n.*881T=
ENST00000528016.1:c.160-7888T= ENSP00000434284.1:n.160-7888T=
ENST00000529059.5:n.1022T=
ENST00000541113.5:c.1005T= ENSP00000442324.1:p.Asp335=
NM_000016.5:c.1113T= NP_000007.1:p.Asp371=
NM_001127328.2:c.1125T= NP_001120800.1:p.Asp375=
NM_001286042.1:c.1005T= NP_001272971.1:p.Asp335=
NM_001286043.1:c.1212T= NP_001272972.1:p.Asp404=
NM_001286044.1:c.546T= NP_001272973.1:p.Asp182=
NM_000016.6:c.1113T= MANE Select NP_000007.1:p.Asp371=
NM_001127328.3:c.1125T= NP_001120800.1:p.Asp375=
NM_001286042.2:c.1005T= NP_001272971.1:p.Asp335=
NM_001286043.2:c.1212T= NP_001272972.1:p.Asp404=
NM_001286044.2:c.546T= NP_001272973.1:p.Asp182=