Canonical Allele Identifier: CA418531913

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76228415A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75762730A>T , CM000663.2:g.75762730A>T	GRCh38
NC_000001.10:g.76228415A>T , CM000663.1:g.76228415A>T	GRCh37
NC_000001.9:g.76001003A>T	NCBI36
NG_007045.2:g.43373A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.1233A>T MANE Select	ENSP00000359878.5:p.Val411=
ENST00000473018.3:n.3357A>T
ENST00000532207.6:n.3565A>T
ENST00000541113.6:c.1137A>T	ENSP00000442324.2:p.Val379=
ENST00000679509.1:n.3516A>T
ENST00000679530.1:c.*1001A>T	ENSP00000506454.1:n.*1001A>T
ENST00000679615.1:n.4569A>T
ENST00000679687.1:c.795A>T	ENSP00000506598.1:p.Val265=
ENST00000679704.1:c.*999A>T	ENSP00000505117.1:n.*999A>T
ENST00000679709.1:c.*1196A>T	ENSP00000506623.1:n.*1196A>T
ENST00000679976.1:c.*817A>T	ENSP00000505565.1:n.*817A>T
ENST00000680166.1:n.4522A>T
ENST00000680582.1:n.2195A>T
ENST00000680613.1:c.*726A>T	ENSP00000506114.1:n.*726A>T
ENST00000680662.1:c.*1147A>T	ENSP00000505080.1:n.*1147A>T
ENST00000680691.1:c.*896A>T	ENSP00000506487.1:n.*896A>T
ENST00000680694.1:c.*821A>T	ENSP00000505658.1:n.*821A>T
ENST00000680743.1:c.*1022A>T	ENSP00000505073.1:n.*1022A>T
ENST00000680749.1:c.*518A>T	ENSP00000505122.1:n.*518A>T
ENST00000680798.1:c.*2029A>T	ENSP00000505670.1:n.*2029A>T
ENST00000680805.1:c.1092A>T	ENSP00000505447.1:p.Val364=
ENST00000680844.1:c.*2338A>T	ENSP00000506541.1:n.*2338A>T
ENST00000680948.1:c.*1100A>T	ENSP00000505441.1:n.*1100A>T
ENST00000680964.1:c.*1647A>T	ENSP00000505961.1:n.*1647A>T
ENST00000681037.1:c.*2717A>T	ENSP00000506025.1:n.*2717A>T
ENST00000681063.1:c.*502A>T	ENSP00000506616.1:n.*502A>T
ENST00000681209.1:c.*888A>T	ENSP00000505877.1:n.*888A>T
ENST00000681278.1:n.1935A>T
ENST00000681289.1:n.5228A>T
ENST00000681361.1:c.*2221A>T	ENSP00000506679.1:n.*2221A>T
ENST00000681430.1:c.*326A>T	ENSP00000506301.1:n.*326A>T
ENST00000681446.1:c.*2258A>T	ENSP00000506244.1:n.*2258A>T
ENST00000681450.1:c.*904A>T	ENSP00000505660.1:n.*904A>T
ENST00000681548.1:c.*2140A>T	ENSP00000505275.1:n.*2140A>T
ENST00000681616.1:c.*2213A>T	ENSP00000505111.1:n.*2213A>T
ENST00000681621.1:c.*2138A>T	ENSP00000505770.1:n.*2138A>T
ENST00000681680.1:n.4649A>T
ENST00000681720.1:c.*688A>T	ENSP00000505438.1:n.*688A>T
ENST00000681730.1:n.1455A>T
ENST00000681790.1:c.975A>T	ENSP00000505130.1:p.Val325=
ENST00000681837.1:n.3170A>T
ENST00000681913.1:n.3479A>T
ENST00000681916.1:c.*1001A>T	ENSP00000506477.1:n.*1001A>T
ENST00000681930.1:n.4678A>T
ENST00000370834.9:c.1332A>T	ENSP00000359871.5:p.Val444=
ENST00000370841.8:c.1233A>T	ENSP00000359878.4:p.Val411=
ENST00000420607.6:c.1245A>T	ENSP00000409612.2:p.Val415=
ENST00000481374.1:n.468-563A>T
ENST00000525808.5:c.*819A>T	ENSP00000434823.1:n.*819A>T
ENST00000526196.5:c.*1001A>T	ENSP00000431953.1:n.*1001A>T
ENST00000528016.1:c.160-6447A>T	ENSP00000434284.1:n.160-6447A>T
ENST00000529059.5:n.1142A>T
ENST00000541113.5:c.1125A>T	ENSP00000442324.1:p.Val375=
NM_000016.5:c.1233A>T	NP_000007.1:p.Val411=
NM_001127328.2:c.1245A>T	NP_001120800.1:p.Val415=
NM_001286042.1:c.1125A>T	NP_001272971.1:p.Val375=
NM_001286043.1:c.1332A>T	NP_001272972.1:p.Val444=
NM_001286044.1:c.666A>T	NP_001272973.1:p.Val222=
NM_000016.6:c.1233A>T MANE Select	NP_000007.1:p.Val411=
NM_001127328.3:c.1245A>T	NP_001120800.1:p.Val415=
NM_001286042.2:c.1125A>T	NP_001272971.1:p.Val375=
NM_001286043.2:c.1332A>T	NP_001272972.1:p.Val444=
NM_001286044.2:c.666A>T	NP_001272973.1:p.Val222=