Canonical Allele Identifier: CA418707709
Gene: ACADM HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.76226971T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761286T>A , CM000663.2:g.75761286T>A GRCh38
NC_000001.10:g.76226971T>A , CM000663.1:g.76226971T>A GRCh37
NC_000001.9:g.75999559T>A NCBI36
NG_007045.2:g.41929T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1110T>A MANE Select ENSP00000359878.5:p.Thr370=
ENST00000473018.3:n.3234T>A
ENST00000532207.6:n.2121T>A
ENST00000541113.6:c.1014T>A ENSP00000442324.2:p.Thr338=
ENST00000679509.1:n.2072T>A
ENST00000679530.1:c.*878T>A ENSP00000506454.1:n.*878T>A
ENST00000679615.1:n.3125T>A
ENST00000679687.1:c.672T>A ENSP00000506598.1:p.Thr224=
ENST00000679704.1:c.*876T>A ENSP00000505117.1:n.*876T>A
ENST00000679709.1:c.*1073T>A ENSP00000506623.1:n.*1073T>A
ENST00000679976.1:c.*694T>A ENSP00000505565.1:n.*694T>A
ENST00000680166.1:n.4399T>A
ENST00000680315.1:n.993T>A
ENST00000680517.1:c.*498T>A ENSP00000505803.1:n.*498T>A
ENST00000680582.1:n.2072T>A
ENST00000680613.1:c.*603T>A ENSP00000506114.1:n.*603T>A
ENST00000680662.1:c.*1024T>A ENSP00000505080.1:n.*1024T>A
ENST00000680691.1:c.*773T>A ENSP00000506487.1:n.*773T>A
ENST00000680694.1:c.*698T>A ENSP00000505658.1:n.*698T>A
ENST00000680743.1:c.*899T>A ENSP00000505073.1:n.*899T>A
ENST00000680749.1:c.*395T>A ENSP00000505122.1:n.*395T>A
ENST00000680798.1:c.*585T>A ENSP00000505670.1:n.*585T>A
ENST00000680805.1:c.969T>A ENSP00000505447.1:p.Thr323=
ENST00000680844.1:c.*894T>A ENSP00000506541.1:n.*894T>A
ENST00000680948.1:c.*977T>A ENSP00000505441.1:n.*977T>A
ENST00000680964.1:c.*203T>A ENSP00000505961.1:n.*203T>A
ENST00000681037.1:c.*2594T>A ENSP00000506025.1:n.*2594T>A
ENST00000681063.1:c.*379T>A ENSP00000506616.1:n.*379T>A
ENST00000681209.1:c.*765T>A ENSP00000505877.1:n.*765T>A
ENST00000681278.1:n.1812T>A
ENST00000681289.1:n.5105T>A
ENST00000681361.1:c.*777T>A ENSP00000506679.1:n.*777T>A
ENST00000681430.1:c.*203T>A ENSP00000506301.1:n.*203T>A
ENST00000681446.1:c.*814T>A ENSP00000506244.1:n.*814T>A
ENST00000681450.1:c.*781T>A ENSP00000505660.1:n.*781T>A
ENST00000681548.1:c.*696T>A ENSP00000505275.1:n.*696T>A
ENST00000681616.1:c.*769T>A ENSP00000505111.1:n.*769T>A
ENST00000681621.1:c.*694T>A ENSP00000505770.1:n.*694T>A
ENST00000681680.1:n.3205T>A
ENST00000681720.1:c.*565T>A ENSP00000505438.1:n.*565T>A
ENST00000681730.1:n.1332T>A
ENST00000681790.1:c.852T>A ENSP00000505130.1:p.Thr284=
ENST00000681837.1:n.1726T>A
ENST00000681913.1:n.3356T>A
ENST00000681916.1:c.*878T>A ENSP00000506477.1:n.*878T>A
ENST00000681930.1:n.3234T>A
ENST00000370834.9:c.1209T>A ENSP00000359871.5:p.Thr403=
ENST00000370841.8:c.1110T>A ENSP00000359878.4:p.Thr370=
ENST00000420607.6:c.1122T>A ENSP00000409612.2:p.Thr374=
ENST00000481374.1:n.383T>A
ENST00000525808.5:c.*696T>A ENSP00000434823.1:n.*696T>A
ENST00000526129.5:c.*894T>A ENSP00000434092.1:n.*894T>A
ENST00000526196.5:c.*878T>A ENSP00000431953.1:n.*878T>A
ENST00000528016.1:c.160-7891T>A ENSP00000434284.1:n.160-7891T>A
ENST00000529059.5:n.1019T>A
ENST00000541113.5:c.1002T>A ENSP00000442324.1:p.Thr334=
NM_000016.5:c.1110T>A NP_000007.1:p.Thr370=
NM_001127328.2:c.1122T>A NP_001120800.1:p.Thr374=
NM_001286042.1:c.1002T>A NP_001272971.1:p.Thr334=
NM_001286043.1:c.1209T>A NP_001272972.1:p.Thr403=
NM_001286044.1:c.543T>A NP_001272973.1:p.Thr181=
NM_000016.6:c.1110T>A MANE Select NP_000007.1:p.Thr370=
NM_001127328.3:c.1122T>A NP_001120800.1:p.Thr374=
NM_001286042.2:c.1002T>A NP_001272971.1:p.Thr334=
NM_001286043.2:c.1209T>A NP_001272972.1:p.Thr403=
NM_001286044.2:c.543T>A NP_001272973.1:p.Thr181=