Canonical Allele Identifier: CA418707830

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76227049C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761364C>T , CM000663.2:g.75761364C>T	GRCh38
NC_000001.10:g.76227049C>T , CM000663.1:g.76227049C>T	GRCh37
NC_000001.9:g.75999637C>T	NCBI36
NG_007045.2:g.42007C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.1188C>T MANE Select	ENSP00000359878.5:p.Ile396=
ENST00000473018.3:n.3312C>T
ENST00000532207.6:n.2199C>T
ENST00000541113.6:c.1092C>T	ENSP00000442324.2:p.Ile364=
ENST00000679509.1:n.2150C>T
ENST00000679530.1:c.*956C>T	ENSP00000506454.1:n.*956C>T
ENST00000679615.1:n.3203C>T
ENST00000679687.1:c.750C>T	ENSP00000506598.1:p.Ile250=
ENST00000679704.1:c.*954C>T	ENSP00000505117.1:n.*954C>T
ENST00000679709.1:c.*1151C>T	ENSP00000506623.1:n.*1151C>T
ENST00000679976.1:c.*772C>T	ENSP00000505565.1:n.*772C>T
ENST00000680166.1:n.4477C>T
ENST00000680315.1:n.1071C>T
ENST00000680517.1:c.*576C>T	ENSP00000505803.1:n.*576C>T
ENST00000680582.1:n.2150C>T
ENST00000680613.1:c.*681C>T	ENSP00000506114.1:n.*681C>T
ENST00000680662.1:c.*1102C>T	ENSP00000505080.1:n.*1102C>T
ENST00000680691.1:c.*851C>T	ENSP00000506487.1:n.*851C>T
ENST00000680694.1:c.*776C>T	ENSP00000505658.1:n.*776C>T
ENST00000680743.1:c.*977C>T	ENSP00000505073.1:n.*977C>T
ENST00000680749.1:c.*473C>T	ENSP00000505122.1:n.*473C>T
ENST00000680798.1:c.*663C>T	ENSP00000505670.1:n.*663C>T
ENST00000680805.1:c.1047C>T	ENSP00000505447.1:p.Ile349=
ENST00000680844.1:c.*972C>T	ENSP00000506541.1:n.*972C>T
ENST00000680948.1:c.*1055C>T	ENSP00000505441.1:n.*1055C>T
ENST00000680964.1:c.*281C>T	ENSP00000505961.1:n.*281C>T
ENST00000681037.1:c.*2672C>T	ENSP00000506025.1:n.*2672C>T
ENST00000681063.1:c.*457C>T	ENSP00000506616.1:n.*457C>T
ENST00000681209.1:c.*843C>T	ENSP00000505877.1:n.*843C>T
ENST00000681278.1:n.1890C>T
ENST00000681289.1:n.5183C>T
ENST00000681361.1:c.*855C>T	ENSP00000506679.1:n.*855C>T
ENST00000681430.1:c.*281C>T	ENSP00000506301.1:n.*281C>T
ENST00000681446.1:c.*892C>T	ENSP00000506244.1:n.*892C>T
ENST00000681450.1:c.*859C>T	ENSP00000505660.1:n.*859C>T
ENST00000681548.1:c.*774C>T	ENSP00000505275.1:n.*774C>T
ENST00000681616.1:c.*847C>T	ENSP00000505111.1:n.*847C>T
ENST00000681621.1:c.*772C>T	ENSP00000505770.1:n.*772C>T
ENST00000681680.1:n.3283C>T
ENST00000681720.1:c.*643C>T	ENSP00000505438.1:n.*643C>T
ENST00000681730.1:n.1410C>T
ENST00000681790.1:c.930C>T	ENSP00000505130.1:p.Ile310=
ENST00000681837.1:n.1804C>T
ENST00000681913.1:n.3434C>T
ENST00000681916.1:c.*956C>T	ENSP00000506477.1:n.*956C>T
ENST00000681930.1:n.3312C>T
ENST00000370834.9:c.1287C>T	ENSP00000359871.5:p.Ile429=
ENST00000370841.8:c.1188C>T	ENSP00000359878.4:p.Ile396=
ENST00000420607.6:c.1200C>T	ENSP00000409612.2:p.Ile400=
ENST00000481374.1:n.461C>T
ENST00000525808.5:c.*774C>T	ENSP00000434823.1:n.*774C>T
ENST00000526129.5:c.*972C>T	ENSP00000434092.1:n.*972C>T
ENST00000526196.5:c.*956C>T	ENSP00000431953.1:n.*956C>T
ENST00000528016.1:c.160-7813C>T	ENSP00000434284.1:n.160-7813C>T
ENST00000529059.5:n.1097C>T
ENST00000541113.5:c.1080C>T	ENSP00000442324.1:p.Ile360=
NM_000016.5:c.1188C>T	NP_000007.1:p.Ile396=
NM_001127328.2:c.1200C>T	NP_001120800.1:p.Ile400=
NM_001286042.1:c.1080C>T	NP_001272971.1:p.Ile360=
NM_001286043.1:c.1287C>T	NP_001272972.1:p.Ile429=
NM_001286044.1:c.621C>T	NP_001272973.1:p.Ile207=
NM_000016.6:c.1188C>T MANE Select	NP_000007.1:p.Ile396=
NM_001127328.3:c.1200C>T	NP_001120800.1:p.Ile400=
NM_001286042.2:c.1080C>T	NP_001272971.1:p.Ile360=
NM_001286043.2:c.1287C>T	NP_001272972.1:p.Ile429=
NM_001286044.2:c.621C>T	NP_001272973.1:p.Ile207=