Canonical Allele Identifier: CA340818028
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761207T>G , CM000663.2:g.75761207T>G GRCh38
NC_000001.10:g.76226892T>G , CM000663.1:g.76226892T>G GRCh37
NC_000001.9:g.75999480T>G NCBI36
NG_007045.2:g.41850T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1031T>G MANE Select ENSP00000359878.5:p.Val344Gly
ENST00000473018.3:n.3155T>G
ENST00000532207.6:n.2042T>G
ENST00000541113.6:c.935T>G ENSP00000442324.2:p.Val312Gly
ENST00000679509.1:n.1993T>G
ENST00000679530.1:c.*799T>G ENSP00000506454.1:n.*799T>G
ENST00000679615.1:n.3046T>G
ENST00000679687.1:c.593T>G ENSP00000506598.1:p.Val198Gly
ENST00000679704.1:c.*797T>G ENSP00000505117.1:n.*797T>G
ENST00000679709.1:c.*994T>G ENSP00000506623.1:n.*994T>G
ENST00000679976.1:c.*615T>G ENSP00000505565.1:n.*615T>G
ENST00000680166.1:n.4320T>G
ENST00000680315.1:n.914T>G
ENST00000680517.1:c.*419T>G ENSP00000505803.1:n.*419T>G
ENST00000680582.1:n.1993T>G
ENST00000680613.1:c.*524T>G ENSP00000506114.1:n.*524T>G
ENST00000680662.1:c.*945T>G ENSP00000505080.1:n.*945T>G
ENST00000680691.1:c.*694T>G ENSP00000506487.1:n.*694T>G
ENST00000680694.1:c.*619T>G ENSP00000505658.1:n.*619T>G
ENST00000680743.1:c.*820T>G ENSP00000505073.1:n.*820T>G
ENST00000680749.1:c.*316T>G ENSP00000505122.1:n.*316T>G
ENST00000680798.1:c.*506T>G ENSP00000505670.1:n.*506T>G
ENST00000680805.1:c.890T>G ENSP00000505447.1:p.Val297Gly
ENST00000680844.1:c.*815T>G ENSP00000506541.1:n.*815T>G
ENST00000680948.1:c.*898T>G ENSP00000505441.1:n.*898T>G
ENST00000680964.1:c.*124T>G ENSP00000505961.1:n.*124T>G
ENST00000681037.1:c.*2515T>G ENSP00000506025.1:n.*2515T>G
ENST00000681063.1:c.*300T>G ENSP00000506616.1:n.*300T>G
ENST00000681209.1:c.*686T>G ENSP00000505877.1:n.*686T>G
ENST00000681278.1:n.1733T>G
ENST00000681289.1:n.5026T>G
ENST00000681361.1:c.*698T>G ENSP00000506679.1:n.*698T>G
ENST00000681430.1:c.*124T>G ENSP00000506301.1:n.*124T>G
ENST00000681446.1:c.*735T>G ENSP00000506244.1:n.*735T>G
ENST00000681450.1:c.*702T>G ENSP00000505660.1:n.*702T>G
ENST00000681548.1:c.*617T>G ENSP00000505275.1:n.*617T>G
ENST00000681616.1:c.*690T>G ENSP00000505111.1:n.*690T>G
ENST00000681621.1:c.*615T>G ENSP00000505770.1:n.*615T>G
ENST00000681680.1:n.3126T>G
ENST00000681720.1:c.*486T>G ENSP00000505438.1:n.*486T>G
ENST00000681730.1:n.1253T>G
ENST00000681790.1:c.773T>G ENSP00000505130.1:p.Val258Gly
ENST00000681837.1:n.1647T>G
ENST00000681913.1:n.3277T>G
ENST00000681916.1:c.*799T>G ENSP00000506477.1:n.*799T>G
ENST00000681930.1:n.3155T>G
ENST00000370834.9:c.1130T>G ENSP00000359871.5:p.Val377Gly
ENST00000370841.8:c.1031T>G ENSP00000359878.4:p.Val344Gly
ENST00000420607.6:c.1043T>G ENSP00000409612.2:p.Val348Gly
ENST00000481374.1:n.304T>G
ENST00000525808.5:c.*617T>G ENSP00000434823.1:n.*617T>G
ENST00000526129.5:c.*815T>G ENSP00000434092.1:n.*815T>G
ENST00000526196.5:c.*799T>G ENSP00000431953.1:n.*799T>G
ENST00000528016.1:c.160-7970T>G ENSP00000434284.1:n.160-7970T>G
ENST00000529059.5:n.940T>G
ENST00000532207.5:n.761T>G
ENST00000534334.5:c.*772T>G ENSP00000435584.1:n.*772T>G
ENST00000541113.5:c.923T>G ENSP00000442324.1:p.Val308Gly
NM_000016.5:c.1031T>G NP_000007.1:p.Val344Gly
NM_001127328.2:c.1043T>G NP_001120800.1:p.Val348Gly
NM_001286042.1:c.923T>G NP_001272971.1:p.Val308Gly
NM_001286043.1:c.1130T>G NP_001272972.1:p.Val377Gly
NM_001286044.1:c.464T>G NP_001272973.1:p.Val155Gly
NM_000016.6:c.1031T>G MANE Select NP_000007.1:p.Val344Gly
NM_001127328.3:c.1043T>G NP_001120800.1:p.Val348Gly
NM_001286042.2:c.923T>G NP_001272971.1:p.Val308Gly
NM_001286043.2:c.1130T>G NP_001272972.1:p.Val377Gly
NM_001286044.2:c.464T>G NP_001272973.1:p.Val155Gly