Canonical Allele Identifier: CA418531849
Gene: ACADM HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.76228406A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75762721A>G , CM000663.2:g.75762721A>G GRCh38
NC_000001.10:g.76228406A>G , CM000663.1:g.76228406A>G GRCh37
NC_000001.9:g.76000994A>G NCBI36
NG_007045.2:g.43364A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1224A>G MANE Select ENSP00000359878.5:p.Arg408=
ENST00000473018.3:n.3348A>G
ENST00000532207.6:n.3556A>G
ENST00000541113.6:c.1128A>G ENSP00000442324.2:p.Arg376=
ENST00000679509.1:n.3507A>G
ENST00000679530.1:c.*992A>G ENSP00000506454.1:n.*992A>G
ENST00000679615.1:n.4560A>G
ENST00000679687.1:c.786A>G ENSP00000506598.1:p.Arg262=
ENST00000679704.1:c.*990A>G ENSP00000505117.1:n.*990A>G
ENST00000679709.1:c.*1187A>G ENSP00000506623.1:n.*1187A>G
ENST00000679976.1:c.*808A>G ENSP00000505565.1:n.*808A>G
ENST00000680166.1:n.4513A>G
ENST00000680582.1:n.2186A>G
ENST00000680613.1:c.*717A>G ENSP00000506114.1:n.*717A>G
ENST00000680662.1:c.*1138A>G ENSP00000505080.1:n.*1138A>G
ENST00000680691.1:c.*887A>G ENSP00000506487.1:n.*887A>G
ENST00000680694.1:c.*812A>G ENSP00000505658.1:n.*812A>G
ENST00000680743.1:c.*1013A>G ENSP00000505073.1:n.*1013A>G
ENST00000680749.1:c.*509A>G ENSP00000505122.1:n.*509A>G
ENST00000680798.1:c.*2020A>G ENSP00000505670.1:n.*2020A>G
ENST00000680805.1:c.1083A>G ENSP00000505447.1:p.Arg361=
ENST00000680844.1:c.*2329A>G ENSP00000506541.1:n.*2329A>G
ENST00000680948.1:c.*1091A>G ENSP00000505441.1:n.*1091A>G
ENST00000680964.1:c.*1638A>G ENSP00000505961.1:n.*1638A>G
ENST00000681037.1:c.*2708A>G ENSP00000506025.1:n.*2708A>G
ENST00000681063.1:c.*493A>G ENSP00000506616.1:n.*493A>G
ENST00000681209.1:c.*879A>G ENSP00000505877.1:n.*879A>G
ENST00000681278.1:n.1926A>G
ENST00000681289.1:n.5219A>G
ENST00000681361.1:c.*2212A>G ENSP00000506679.1:n.*2212A>G
ENST00000681430.1:c.*317A>G ENSP00000506301.1:n.*317A>G
ENST00000681446.1:c.*2249A>G ENSP00000506244.1:n.*2249A>G
ENST00000681450.1:c.*895A>G ENSP00000505660.1:n.*895A>G
ENST00000681548.1:c.*2131A>G ENSP00000505275.1:n.*2131A>G
ENST00000681616.1:c.*2204A>G ENSP00000505111.1:n.*2204A>G
ENST00000681621.1:c.*2129A>G ENSP00000505770.1:n.*2129A>G
ENST00000681680.1:n.4640A>G
ENST00000681720.1:c.*679A>G ENSP00000505438.1:n.*679A>G
ENST00000681730.1:n.1446A>G
ENST00000681790.1:c.966A>G ENSP00000505130.1:p.Arg322=
ENST00000681837.1:n.3161A>G
ENST00000681913.1:n.3470A>G
ENST00000681916.1:c.*992A>G ENSP00000506477.1:n.*992A>G
ENST00000681930.1:n.4669A>G
ENST00000370834.9:c.1323A>G ENSP00000359871.5:p.Arg441=
ENST00000370841.8:c.1224A>G ENSP00000359878.4:p.Arg408=
ENST00000420607.6:c.1236A>G ENSP00000409612.2:p.Arg412=
ENST00000481374.1:n.468-572A>G
ENST00000525808.5:c.*810A>G ENSP00000434823.1:n.*810A>G
ENST00000526196.5:c.*992A>G ENSP00000431953.1:n.*992A>G
ENST00000528016.1:c.160-6456A>G ENSP00000434284.1:n.160-6456A>G
ENST00000529059.5:n.1133A>G
ENST00000541113.5:c.1116A>G ENSP00000442324.1:p.Arg372=
NM_000016.5:c.1224A>G NP_000007.1:p.Arg408=
NM_001127328.2:c.1236A>G NP_001120800.1:p.Arg412=
NM_001286042.1:c.1116A>G NP_001272971.1:p.Arg372=
NM_001286043.1:c.1323A>G NP_001272972.1:p.Arg441=
NM_001286044.1:c.657A>G NP_001272973.1:p.Arg219=
NM_000016.6:c.1224A>G MANE Select NP_000007.1:p.Arg408=
NM_001127328.3:c.1236A>G NP_001120800.1:p.Arg412=
NM_001286042.2:c.1116A>G NP_001272971.1:p.Arg372=
NM_001286043.2:c.1323A>G NP_001272972.1:p.Arg441=
NM_001286044.2:c.657A>G NP_001272973.1:p.Arg219=