Canonical Allele Identifier: CA418707727
Gene: ACADM HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.76226983G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761298G>A , CM000663.2:g.75761298G>A GRCh38
NC_000001.10:g.76226983G>A , CM000663.1:g.76226983G>A GRCh37
NC_000001.9:g.75999571G>A NCBI36
NG_007045.2:g.41941G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1122G>A MANE Select ENSP00000359878.5:p.Gln374=
ENST00000473018.3:n.3246G>A
ENST00000532207.6:n.2133G>A
ENST00000541113.6:c.1026G>A ENSP00000442324.2:p.Gln342=
ENST00000679509.1:n.2084G>A
ENST00000679530.1:c.*890G>A ENSP00000506454.1:n.*890G>A
ENST00000679615.1:n.3137G>A
ENST00000679687.1:c.684G>A ENSP00000506598.1:p.Gln228=
ENST00000679704.1:c.*888G>A ENSP00000505117.1:n.*888G>A
ENST00000679709.1:c.*1085G>A ENSP00000506623.1:n.*1085G>A
ENST00000679976.1:c.*706G>A ENSP00000505565.1:n.*706G>A
ENST00000680166.1:n.4411G>A
ENST00000680315.1:n.1005G>A
ENST00000680517.1:c.*510G>A ENSP00000505803.1:n.*510G>A
ENST00000680582.1:n.2084G>A
ENST00000680613.1:c.*615G>A ENSP00000506114.1:n.*615G>A
ENST00000680662.1:c.*1036G>A ENSP00000505080.1:n.*1036G>A
ENST00000680691.1:c.*785G>A ENSP00000506487.1:n.*785G>A
ENST00000680694.1:c.*710G>A ENSP00000505658.1:n.*710G>A
ENST00000680743.1:c.*911G>A ENSP00000505073.1:n.*911G>A
ENST00000680749.1:c.*407G>A ENSP00000505122.1:n.*407G>A
ENST00000680798.1:c.*597G>A ENSP00000505670.1:n.*597G>A
ENST00000680805.1:c.981G>A ENSP00000505447.1:p.Gln327=
ENST00000680844.1:c.*906G>A ENSP00000506541.1:n.*906G>A
ENST00000680948.1:c.*989G>A ENSP00000505441.1:n.*989G>A
ENST00000680964.1:c.*215G>A ENSP00000505961.1:n.*215G>A
ENST00000681037.1:c.*2606G>A ENSP00000506025.1:n.*2606G>A
ENST00000681063.1:c.*391G>A ENSP00000506616.1:n.*391G>A
ENST00000681209.1:c.*777G>A ENSP00000505877.1:n.*777G>A
ENST00000681278.1:n.1824G>A
ENST00000681289.1:n.5117G>A
ENST00000681361.1:c.*789G>A ENSP00000506679.1:n.*789G>A
ENST00000681430.1:c.*215G>A ENSP00000506301.1:n.*215G>A
ENST00000681446.1:c.*826G>A ENSP00000506244.1:n.*826G>A
ENST00000681450.1:c.*793G>A ENSP00000505660.1:n.*793G>A
ENST00000681548.1:c.*708G>A ENSP00000505275.1:n.*708G>A
ENST00000681616.1:c.*781G>A ENSP00000505111.1:n.*781G>A
ENST00000681621.1:c.*706G>A ENSP00000505770.1:n.*706G>A
ENST00000681680.1:n.3217G>A
ENST00000681720.1:c.*577G>A ENSP00000505438.1:n.*577G>A
ENST00000681730.1:n.1344G>A
ENST00000681790.1:c.864G>A ENSP00000505130.1:p.Gln288=
ENST00000681837.1:n.1738G>A
ENST00000681913.1:n.3368G>A
ENST00000681916.1:c.*890G>A ENSP00000506477.1:n.*890G>A
ENST00000681930.1:n.3246G>A
ENST00000370834.9:c.1221G>A ENSP00000359871.5:p.Gln407=
ENST00000370841.8:c.1122G>A ENSP00000359878.4:p.Gln374=
ENST00000420607.6:c.1134G>A ENSP00000409612.2:p.Gln378=
ENST00000481374.1:n.395G>A
ENST00000525808.5:c.*708G>A ENSP00000434823.1:n.*708G>A
ENST00000526129.5:c.*906G>A ENSP00000434092.1:n.*906G>A
ENST00000526196.5:c.*890G>A ENSP00000431953.1:n.*890G>A
ENST00000528016.1:c.160-7879G>A ENSP00000434284.1:n.160-7879G>A
ENST00000529059.5:n.1031G>A
ENST00000541113.5:c.1014G>A ENSP00000442324.1:p.Gln338=
NM_000016.5:c.1122G>A NP_000007.1:p.Gln374=
NM_001127328.2:c.1134G>A NP_001120800.1:p.Gln378=
NM_001286042.1:c.1014G>A NP_001272971.1:p.Gln338=
NM_001286043.1:c.1221G>A NP_001272972.1:p.Gln407=
NM_001286044.1:c.555G>A NP_001272973.1:p.Gln185=
NM_000016.6:c.1122G>A MANE Select NP_000007.1:p.Gln374=
NM_001127328.3:c.1134G>A NP_001120800.1:p.Gln378=
NM_001286042.2:c.1014G>A NP_001272971.1:p.Gln338=
NM_001286043.2:c.1221G>A NP_001272972.1:p.Gln407=
NM_001286044.2:c.555G>A NP_001272973.1:p.Gln185=