Canonical Allele Identifier: CA418707636
Gene: ACADM HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.76226929T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761244T>A , CM000663.2:g.75761244T>A GRCh38
NC_000001.10:g.76226929T>A , CM000663.1:g.76226929T>A GRCh37
NC_000001.9:g.75999517T>A NCBI36
NG_007045.2:g.41887T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1068T>A MANE Select ENSP00000359878.5:p.Ile356=
ENST00000473018.3:n.3192T>A
ENST00000532207.6:n.2079T>A
ENST00000541113.6:c.972T>A ENSP00000442324.2:p.Ile324=
ENST00000679509.1:n.2030T>A
ENST00000679530.1:c.*836T>A ENSP00000506454.1:n.*836T>A
ENST00000679615.1:n.3083T>A
ENST00000679687.1:c.630T>A ENSP00000506598.1:p.Ile210=
ENST00000679704.1:c.*834T>A ENSP00000505117.1:n.*834T>A
ENST00000679709.1:c.*1031T>A ENSP00000506623.1:n.*1031T>A
ENST00000679976.1:c.*652T>A ENSP00000505565.1:n.*652T>A
ENST00000680166.1:n.4357T>A
ENST00000680315.1:n.951T>A
ENST00000680517.1:c.*456T>A ENSP00000505803.1:n.*456T>A
ENST00000680582.1:n.2030T>A
ENST00000680613.1:c.*561T>A ENSP00000506114.1:n.*561T>A
ENST00000680662.1:c.*982T>A ENSP00000505080.1:n.*982T>A
ENST00000680691.1:c.*731T>A ENSP00000506487.1:n.*731T>A
ENST00000680694.1:c.*656T>A ENSP00000505658.1:n.*656T>A
ENST00000680743.1:c.*857T>A ENSP00000505073.1:n.*857T>A
ENST00000680749.1:c.*353T>A ENSP00000505122.1:n.*353T>A
ENST00000680798.1:c.*543T>A ENSP00000505670.1:n.*543T>A
ENST00000680805.1:c.927T>A ENSP00000505447.1:p.Ile309=
ENST00000680844.1:c.*852T>A ENSP00000506541.1:n.*852T>A
ENST00000680948.1:c.*935T>A ENSP00000505441.1:n.*935T>A
ENST00000680964.1:c.*161T>A ENSP00000505961.1:n.*161T>A
ENST00000681037.1:c.*2552T>A ENSP00000506025.1:n.*2552T>A
ENST00000681063.1:c.*337T>A ENSP00000506616.1:n.*337T>A
ENST00000681209.1:c.*723T>A ENSP00000505877.1:n.*723T>A
ENST00000681278.1:n.1770T>A
ENST00000681289.1:n.5063T>A
ENST00000681361.1:c.*735T>A ENSP00000506679.1:n.*735T>A
ENST00000681430.1:c.*161T>A ENSP00000506301.1:n.*161T>A
ENST00000681446.1:c.*772T>A ENSP00000506244.1:n.*772T>A
ENST00000681450.1:c.*739T>A ENSP00000505660.1:n.*739T>A
ENST00000681548.1:c.*654T>A ENSP00000505275.1:n.*654T>A
ENST00000681616.1:c.*727T>A ENSP00000505111.1:n.*727T>A
ENST00000681621.1:c.*652T>A ENSP00000505770.1:n.*652T>A
ENST00000681680.1:n.3163T>A
ENST00000681720.1:c.*523T>A ENSP00000505438.1:n.*523T>A
ENST00000681730.1:n.1290T>A
ENST00000681790.1:c.810T>A ENSP00000505130.1:p.Ile270=
ENST00000681837.1:n.1684T>A
ENST00000681913.1:n.3314T>A
ENST00000681916.1:c.*836T>A ENSP00000506477.1:n.*836T>A
ENST00000681930.1:n.3192T>A
ENST00000370834.9:c.1167T>A ENSP00000359871.5:p.Ile389=
ENST00000370841.8:c.1068T>A ENSP00000359878.4:p.Ile356=
ENST00000420607.6:c.1080T>A ENSP00000409612.2:p.Ile360=
ENST00000481374.1:n.341T>A
ENST00000525808.5:c.*654T>A ENSP00000434823.1:n.*654T>A
ENST00000526129.5:c.*852T>A ENSP00000434092.1:n.*852T>A
ENST00000526196.5:c.*836T>A ENSP00000431953.1:n.*836T>A
ENST00000528016.1:c.160-7933T>A ENSP00000434284.1:n.160-7933T>A
ENST00000529059.5:n.977T>A
ENST00000534334.5:c.*809T>A ENSP00000435584.1:n.*809T>A
ENST00000541113.5:c.960T>A ENSP00000442324.1:p.Ile320=
NM_000016.5:c.1068T>A NP_000007.1:p.Ile356=
NM_001127328.2:c.1080T>A NP_001120800.1:p.Ile360=
NM_001286042.1:c.960T>A NP_001272971.1:p.Ile320=
NM_001286043.1:c.1167T>A NP_001272972.1:p.Ile389=
NM_001286044.1:c.501T>A NP_001272973.1:p.Ile167=
NM_000016.6:c.1068T>A MANE Select NP_000007.1:p.Ile356=
NM_001127328.3:c.1080T>A NP_001120800.1:p.Ile360=
NM_001286042.2:c.960T>A NP_001272971.1:p.Ile320=
NM_001286043.2:c.1167T>A NP_001272972.1:p.Ile389=
NM_001286044.2:c.501T>A NP_001272973.1:p.Ile167=