Canonical Allele Identifier: CA340818188
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761285C>A , CM000663.2:g.75761285C>A GRCh38
NC_000001.10:g.76226970C>A , CM000663.1:g.76226970C>A GRCh37
NC_000001.9:g.75999558C>A NCBI36
NG_007045.2:g.41928C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1109C>A MANE Select ENSP00000359878.5:p.Thr370Asn
ENST00000473018.3:n.3233C>A
ENST00000532207.6:n.2120C>A
ENST00000541113.6:c.1013C>A ENSP00000442324.2:p.Thr338Asn
ENST00000679509.1:n.2071C>A
ENST00000679530.1:c.*877C>A ENSP00000506454.1:n.*877C>A
ENST00000679615.1:n.3124C>A
ENST00000679687.1:c.671C>A ENSP00000506598.1:p.Thr224Asn
ENST00000679704.1:c.*875C>A ENSP00000505117.1:n.*875C>A
ENST00000679709.1:c.*1072C>A ENSP00000506623.1:n.*1072C>A
ENST00000679976.1:c.*693C>A ENSP00000505565.1:n.*693C>A
ENST00000680166.1:n.4398C>A
ENST00000680315.1:n.992C>A
ENST00000680517.1:c.*497C>A ENSP00000505803.1:n.*497C>A
ENST00000680582.1:n.2071C>A
ENST00000680613.1:c.*602C>A ENSP00000506114.1:n.*602C>A
ENST00000680662.1:c.*1023C>A ENSP00000505080.1:n.*1023C>A
ENST00000680691.1:c.*772C>A ENSP00000506487.1:n.*772C>A
ENST00000680694.1:c.*697C>A ENSP00000505658.1:n.*697C>A
ENST00000680743.1:c.*898C>A ENSP00000505073.1:n.*898C>A
ENST00000680749.1:c.*394C>A ENSP00000505122.1:n.*394C>A
ENST00000680798.1:c.*584C>A ENSP00000505670.1:n.*584C>A
ENST00000680805.1:c.968C>A ENSP00000505447.1:p.Thr323Asn
ENST00000680844.1:c.*893C>A ENSP00000506541.1:n.*893C>A
ENST00000680948.1:c.*976C>A ENSP00000505441.1:n.*976C>A
ENST00000680964.1:c.*202C>A ENSP00000505961.1:n.*202C>A
ENST00000681037.1:c.*2593C>A ENSP00000506025.1:n.*2593C>A
ENST00000681063.1:c.*378C>A ENSP00000506616.1:n.*378C>A
ENST00000681209.1:c.*764C>A ENSP00000505877.1:n.*764C>A
ENST00000681278.1:n.1811C>A
ENST00000681289.1:n.5104C>A
ENST00000681361.1:c.*776C>A ENSP00000506679.1:n.*776C>A
ENST00000681430.1:c.*202C>A ENSP00000506301.1:n.*202C>A
ENST00000681446.1:c.*813C>A ENSP00000506244.1:n.*813C>A
ENST00000681450.1:c.*780C>A ENSP00000505660.1:n.*780C>A
ENST00000681548.1:c.*695C>A ENSP00000505275.1:n.*695C>A
ENST00000681616.1:c.*768C>A ENSP00000505111.1:n.*768C>A
ENST00000681621.1:c.*693C>A ENSP00000505770.1:n.*693C>A
ENST00000681680.1:n.3204C>A
ENST00000681720.1:c.*564C>A ENSP00000505438.1:n.*564C>A
ENST00000681730.1:n.1331C>A
ENST00000681790.1:c.851C>A ENSP00000505130.1:p.Thr284Asn
ENST00000681837.1:n.1725C>A
ENST00000681913.1:n.3355C>A
ENST00000681916.1:c.*877C>A ENSP00000506477.1:n.*877C>A
ENST00000681930.1:n.3233C>A
ENST00000370834.9:c.1208C>A ENSP00000359871.5:p.Thr403Asn
ENST00000370841.8:c.1109C>A ENSP00000359878.4:p.Thr370Asn
ENST00000420607.6:c.1121C>A ENSP00000409612.2:p.Thr374Asn
ENST00000481374.1:n.382C>A
ENST00000525808.5:c.*695C>A ENSP00000434823.1:n.*695C>A
ENST00000526129.5:c.*893C>A ENSP00000434092.1:n.*893C>A
ENST00000526196.5:c.*877C>A ENSP00000431953.1:n.*877C>A
ENST00000528016.1:c.160-7892C>A ENSP00000434284.1:n.160-7892C>A
ENST00000529059.5:n.1018C>A
ENST00000541113.5:c.1001C>A ENSP00000442324.1:p.Thr334Asn
NM_000016.5:c.1109C>A NP_000007.1:p.Thr370Asn
NM_001127328.2:c.1121C>A NP_001120800.1:p.Thr374Asn
NM_001286042.1:c.1001C>A NP_001272971.1:p.Thr334Asn
NM_001286043.1:c.1208C>A NP_001272972.1:p.Thr403Asn
NM_001286044.1:c.542C>A NP_001272973.1:p.Thr181Asn
NM_000016.6:c.1109C>A MANE Select NP_000007.1:p.Thr370Asn
NM_001127328.3:c.1121C>A NP_001120800.1:p.Thr374Asn
NM_001286042.2:c.1001C>A NP_001272971.1:p.Thr334Asn
NM_001286043.2:c.1208C>A NP_001272972.1:p.Thr403Asn
NM_001286044.2:c.542C>A NP_001272973.1:p.Thr181Asn