Canonical Allele Identifier: CA1176721850
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75750447C= , CM000663.2:g.75750447C= GRCh38
NC_000001.10:g.76216132C= , CM000663.1:g.76216132C= GRCh37
NC_000001.9:g.75988720C= NCBI36
NG_007045.2:g.31090C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.850-4C= MANE Select ENSP00000359878.5:n.850-4C=
ENST00000473018.3:n.2974-4C=
ENST00000532207.6:n.1739-4C=
ENST00000541113.6:c.849+888C= ENSP00000442324.2:n.849+888C=
ENST00000679509.1:n.1812-4C=
ENST00000679530.1:c.*618-4C= ENSP00000506454.1:n.*618-4C=
ENST00000679615.1:n.2865-4C=
ENST00000679687.1:c.412-4C= ENSP00000506598.1:n.412-4C=
ENST00000679704.1:c.*616-4C= ENSP00000505117.1:n.*616-4C=
ENST00000679709.1:c.*813-4C= ENSP00000506623.1:n.*813-4C=
ENST00000679976.1:c.*434-4C= ENSP00000505565.1:n.*434-4C=
ENST00000680166.1:n.4139-4C=
ENST00000680315.1:n.729C=
ENST00000680517.1:c.*238-4C= ENSP00000505803.1:n.*238-4C=
ENST00000680582.1:n.1812-4C=
ENST00000680613.1:c.*221-4C= ENSP00000506114.1:n.*221-4C=
ENST00000680662.1:c.*764-4C= ENSP00000505080.1:n.*764-4C=
ENST00000680691.1:c.*513-4C= ENSP00000506487.1:n.*513-4C=
ENST00000680694.1:c.*438-4C= ENSP00000505658.1:n.*438-4C=
ENST00000680743.1:c.*517-4C= ENSP00000505073.1:n.*517-4C=
ENST00000680749.1:c.*135-4C= ENSP00000505122.1:n.*135-4C=
ENST00000680798.1:c.*325-4C= ENSP00000505670.1:n.*325-4C=
ENST00000680805.1:c.709-4C= ENSP00000505447.1:n.709-4C=
ENST00000680844.1:c.*634-4C= ENSP00000506541.1:n.*634-4C=
ENST00000680948.1:c.*717-4C= ENSP00000505441.1:n.*717-4C=
ENST00000680964.1:c.850-4C= ENSP00000505961.1:n.850-4C=
ENST00000681037.1:c.*2334-4C= ENSP00000506025.1:n.*2334-4C=
ENST00000681063.1:c.600-4C= ENSP00000506616.1:n.600-4C=
ENST00000681209.1:c.*505-4C= ENSP00000505877.1:n.*505-4C=
ENST00000681278.1:n.1207-4C=
ENST00000681289.1:n.4845-4C=
ENST00000681361.1:c.*517-4C= ENSP00000506679.1:n.*517-4C=
ENST00000681430.1:c.850-4C= ENSP00000506301.1:n.850-4C=
ENST00000681446.1:c.*432-4C= ENSP00000506244.1:n.*432-4C=
ENST00000681450.1:c.*521-4C= ENSP00000505660.1:n.*521-4C=
ENST00000681548.1:c.*436-4C= ENSP00000505275.1:n.*436-4C=
ENST00000681616.1:c.*509-4C= ENSP00000505111.1:n.*509-4C=
ENST00000681621.1:c.*434-4C= ENSP00000505770.1:n.*434-4C=
ENST00000681680.1:n.2945-4C=
ENST00000681720.1:c.*305-4C= ENSP00000505438.1:n.*305-4C=
ENST00000681730.1:n.1072-4C=
ENST00000681790.1:c.592-4C= ENSP00000505130.1:n.592-4C=
ENST00000681837.1:n.1466-4C=
ENST00000681913.1:n.2974-4C=
ENST00000681916.1:c.*618-4C= ENSP00000506477.1:n.*618-4C=
ENST00000681930.1:n.2974-4C=
ENST00000370834.9:c.949-4C= ENSP00000359871.5:n.949-4C=
ENST00000370841.8:c.850-4C= ENSP00000359878.4:n.850-4C=
ENST00000420607.6:c.862-4C= ENSP00000409612.2:n.862-4C=
ENST00000525808.5:c.*436-4C= ENSP00000434823.1:n.*436-4C=
ENST00000526129.5:c.*634-4C= ENSP00000434092.1:n.*634-4C=
ENST00000526196.5:c.*618-4C= ENSP00000431953.1:n.*618-4C=
ENST00000528016.1:c.64-4C= ENSP00000434284.1:n.64-4C=
ENST00000529059.5:n.759-4C=
ENST00000532207.5:n.580-4C=
ENST00000534334.5:c.*434-4C= ENSP00000435584.1:n.*434-4C=
ENST00000541113.5:c.742-4C= ENSP00000442324.1:n.742-4C=
NM_000016.5:c.850-4C= NP_000007.1:n.850-4C=
NM_001127328.2:c.862-4C= NP_001120800.1:n.862-4C=
NM_001286042.1:c.742-4C= NP_001272971.1:n.742-4C=
NM_001286043.1:c.949-4C= NP_001272972.1:n.949-4C=
NM_001286044.1:c.283-4C= NP_001272973.1:n.283-4C=
NM_000016.6:c.850-4C= MANE Select NP_000007.1:n.850-4C=
NM_001127328.3:c.862-4C= NP_001120800.1:n.862-4C=
NM_001286042.2:c.742-4C= NP_001272971.1:n.742-4C=
NM_001286043.2:c.949-4C= NP_001272972.1:n.949-4C=
NM_001286044.2:c.283-4C= NP_001272973.1:n.283-4C=