Canonical Allele Identifier: CA340818207
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761296C>A , CM000663.2:g.75761296C>A GRCh38
NC_000001.10:g.76226981C>A , CM000663.1:g.76226981C>A GRCh37
NC_000001.9:g.75999569C>A NCBI36
NG_007045.2:g.41939C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1120C>A MANE Select ENSP00000359878.5:p.Gln374Lys
ENST00000473018.3:n.3244C>A
ENST00000532207.6:n.2131C>A
ENST00000541113.6:c.1024C>A ENSP00000442324.2:p.Gln342Lys
ENST00000679509.1:n.2082C>A
ENST00000679530.1:c.*888C>A ENSP00000506454.1:n.*888C>A
ENST00000679615.1:n.3135C>A
ENST00000679687.1:c.682C>A ENSP00000506598.1:p.Gln228Lys
ENST00000679704.1:c.*886C>A ENSP00000505117.1:n.*886C>A
ENST00000679709.1:c.*1083C>A ENSP00000506623.1:n.*1083C>A
ENST00000679976.1:c.*704C>A ENSP00000505565.1:n.*704C>A
ENST00000680166.1:n.4409C>A
ENST00000680315.1:n.1003C>A
ENST00000680517.1:c.*508C>A ENSP00000505803.1:n.*508C>A
ENST00000680582.1:n.2082C>A
ENST00000680613.1:c.*613C>A ENSP00000506114.1:n.*613C>A
ENST00000680662.1:c.*1034C>A ENSP00000505080.1:n.*1034C>A
ENST00000680691.1:c.*783C>A ENSP00000506487.1:n.*783C>A
ENST00000680694.1:c.*708C>A ENSP00000505658.1:n.*708C>A
ENST00000680743.1:c.*909C>A ENSP00000505073.1:n.*909C>A
ENST00000680749.1:c.*405C>A ENSP00000505122.1:n.*405C>A
ENST00000680798.1:c.*595C>A ENSP00000505670.1:n.*595C>A
ENST00000680805.1:c.979C>A ENSP00000505447.1:p.Gln327Lys
ENST00000680844.1:c.*904C>A ENSP00000506541.1:n.*904C>A
ENST00000680948.1:c.*987C>A ENSP00000505441.1:n.*987C>A
ENST00000680964.1:c.*213C>A ENSP00000505961.1:n.*213C>A
ENST00000681037.1:c.*2604C>A ENSP00000506025.1:n.*2604C>A
ENST00000681063.1:c.*389C>A ENSP00000506616.1:n.*389C>A
ENST00000681209.1:c.*775C>A ENSP00000505877.1:n.*775C>A
ENST00000681278.1:n.1822C>A
ENST00000681289.1:n.5115C>A
ENST00000681361.1:c.*787C>A ENSP00000506679.1:n.*787C>A
ENST00000681430.1:c.*213C>A ENSP00000506301.1:n.*213C>A
ENST00000681446.1:c.*824C>A ENSP00000506244.1:n.*824C>A
ENST00000681450.1:c.*791C>A ENSP00000505660.1:n.*791C>A
ENST00000681548.1:c.*706C>A ENSP00000505275.1:n.*706C>A
ENST00000681616.1:c.*779C>A ENSP00000505111.1:n.*779C>A
ENST00000681621.1:c.*704C>A ENSP00000505770.1:n.*704C>A
ENST00000681680.1:n.3215C>A
ENST00000681720.1:c.*575C>A ENSP00000505438.1:n.*575C>A
ENST00000681730.1:n.1342C>A
ENST00000681790.1:c.862C>A ENSP00000505130.1:p.Gln288Lys
ENST00000681837.1:n.1736C>A
ENST00000681913.1:n.3366C>A
ENST00000681916.1:c.*888C>A ENSP00000506477.1:n.*888C>A
ENST00000681930.1:n.3244C>A
ENST00000370834.9:c.1219C>A ENSP00000359871.5:p.Gln407Lys
ENST00000370841.8:c.1120C>A ENSP00000359878.4:p.Gln374Lys
ENST00000420607.6:c.1132C>A ENSP00000409612.2:p.Gln378Lys
ENST00000481374.1:n.393C>A
ENST00000525808.5:c.*706C>A ENSP00000434823.1:n.*706C>A
ENST00000526129.5:c.*904C>A ENSP00000434092.1:n.*904C>A
ENST00000526196.5:c.*888C>A ENSP00000431953.1:n.*888C>A
ENST00000528016.1:c.160-7881C>A ENSP00000434284.1:n.160-7881C>A
ENST00000529059.5:n.1029C>A
ENST00000541113.5:c.1012C>A ENSP00000442324.1:p.Gln338Lys
NM_000016.5:c.1120C>A NP_000007.1:p.Gln374Lys
NM_001127328.2:c.1132C>A NP_001120800.1:p.Gln378Lys
NM_001286042.1:c.1012C>A NP_001272971.1:p.Gln338Lys
NM_001286043.1:c.1219C>A NP_001272972.1:p.Gln407Lys
NM_001286044.1:c.553C>A NP_001272973.1:p.Gln185Lys
NM_000016.6:c.1120C>A MANE Select NP_000007.1:p.Gln374Lys
NM_001127328.3:c.1132C>A NP_001120800.1:p.Gln378Lys
NM_001286042.2:c.1012C>A NP_001272971.1:p.Gln338Lys
NM_001286043.2:c.1219C>A NP_001272972.1:p.Gln407Lys
NM_001286044.2:c.553C>A NP_001272973.1:p.Gln185Lys