Canonical Allele Identifier: CA418531871
Gene: ACADM HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.76228409T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75762724T>A , CM000663.2:g.75762724T>A GRCh38
NC_000001.10:g.76228409T>A , CM000663.1:g.76228409T>A GRCh37
NC_000001.9:g.76000997T>A NCBI36
NG_007045.2:g.43367T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1227T>A MANE Select ENSP00000359878.5:p.Leu409=
ENST00000473018.3:n.3351T>A
ENST00000532207.6:n.3559T>A
ENST00000541113.6:c.1131T>A ENSP00000442324.2:p.Leu377=
ENST00000679509.1:n.3510T>A
ENST00000679530.1:c.*995T>A ENSP00000506454.1:n.*995T>A
ENST00000679615.1:n.4563T>A
ENST00000679687.1:c.789T>A ENSP00000506598.1:p.Leu263=
ENST00000679704.1:c.*993T>A ENSP00000505117.1:n.*993T>A
ENST00000679709.1:c.*1190T>A ENSP00000506623.1:n.*1190T>A
ENST00000679976.1:c.*811T>A ENSP00000505565.1:n.*811T>A
ENST00000680166.1:n.4516T>A
ENST00000680582.1:n.2189T>A
ENST00000680613.1:c.*720T>A ENSP00000506114.1:n.*720T>A
ENST00000680662.1:c.*1141T>A ENSP00000505080.1:n.*1141T>A
ENST00000680691.1:c.*890T>A ENSP00000506487.1:n.*890T>A
ENST00000680694.1:c.*815T>A ENSP00000505658.1:n.*815T>A
ENST00000680743.1:c.*1016T>A ENSP00000505073.1:n.*1016T>A
ENST00000680749.1:c.*512T>A ENSP00000505122.1:n.*512T>A
ENST00000680798.1:c.*2023T>A ENSP00000505670.1:n.*2023T>A
ENST00000680805.1:c.1086T>A ENSP00000505447.1:p.Leu362=
ENST00000680844.1:c.*2332T>A ENSP00000506541.1:n.*2332T>A
ENST00000680948.1:c.*1094T>A ENSP00000505441.1:n.*1094T>A
ENST00000680964.1:c.*1641T>A ENSP00000505961.1:n.*1641T>A
ENST00000681037.1:c.*2711T>A ENSP00000506025.1:n.*2711T>A
ENST00000681063.1:c.*496T>A ENSP00000506616.1:n.*496T>A
ENST00000681209.1:c.*882T>A ENSP00000505877.1:n.*882T>A
ENST00000681278.1:n.1929T>A
ENST00000681289.1:n.5222T>A
ENST00000681361.1:c.*2215T>A ENSP00000506679.1:n.*2215T>A
ENST00000681430.1:c.*320T>A ENSP00000506301.1:n.*320T>A
ENST00000681446.1:c.*2252T>A ENSP00000506244.1:n.*2252T>A
ENST00000681450.1:c.*898T>A ENSP00000505660.1:n.*898T>A
ENST00000681548.1:c.*2134T>A ENSP00000505275.1:n.*2134T>A
ENST00000681616.1:c.*2207T>A ENSP00000505111.1:n.*2207T>A
ENST00000681621.1:c.*2132T>A ENSP00000505770.1:n.*2132T>A
ENST00000681680.1:n.4643T>A
ENST00000681720.1:c.*682T>A ENSP00000505438.1:n.*682T>A
ENST00000681730.1:n.1449T>A
ENST00000681790.1:c.969T>A ENSP00000505130.1:p.Leu323=
ENST00000681837.1:n.3164T>A
ENST00000681913.1:n.3473T>A
ENST00000681916.1:c.*995T>A ENSP00000506477.1:n.*995T>A
ENST00000681930.1:n.4672T>A
ENST00000370834.9:c.1326T>A ENSP00000359871.5:p.Leu442=
ENST00000370841.8:c.1227T>A ENSP00000359878.4:p.Leu409=
ENST00000420607.6:c.1239T>A ENSP00000409612.2:p.Leu413=
ENST00000481374.1:n.468-569T>A
ENST00000525808.5:c.*813T>A ENSP00000434823.1:n.*813T>A
ENST00000526196.5:c.*995T>A ENSP00000431953.1:n.*995T>A
ENST00000528016.1:c.160-6453T>A ENSP00000434284.1:n.160-6453T>A
ENST00000529059.5:n.1136T>A
ENST00000541113.5:c.1119T>A ENSP00000442324.1:p.Leu373=
NM_000016.5:c.1227T>A NP_000007.1:p.Leu409=
NM_001127328.2:c.1239T>A NP_001120800.1:p.Leu413=
NM_001286042.1:c.1119T>A NP_001272971.1:p.Leu373=
NM_001286043.1:c.1326T>A NP_001272972.1:p.Leu442=
NM_001286044.1:c.660T>A NP_001272973.1:p.Leu220=
NM_000016.6:c.1227T>A MANE Select NP_000007.1:p.Leu409=
NM_001127328.3:c.1239T>A NP_001120800.1:p.Leu413=
NM_001286042.2:c.1119T>A NP_001272971.1:p.Leu373=
NM_001286043.2:c.1326T>A NP_001272972.1:p.Leu442=
NM_001286044.2:c.660T>A NP_001272973.1:p.Leu220=