Canonical Allele Identifier: CA418707582

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226902T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761217T>C , CM000663.2:g.75761217T>C	GRCh38
NC_000001.10:g.76226902T>C , CM000663.1:g.76226902T>C	GRCh37
NC_000001.9:g.75999490T>C	NCBI36
NG_007045.2:g.41860T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.1041T>C MANE Select	ENSP00000359878.5:p.Gly347=
ENST00000473018.3:n.3165T>C
ENST00000532207.6:n.2052T>C
ENST00000541113.6:c.945T>C	ENSP00000442324.2:p.Gly315=
ENST00000679509.1:n.2003T>C
ENST00000679530.1:c.*809T>C	ENSP00000506454.1:n.*809T>C
ENST00000679615.1:n.3056T>C
ENST00000679687.1:c.603T>C	ENSP00000506598.1:p.Gly201=
ENST00000679704.1:c.*807T>C	ENSP00000505117.1:n.*807T>C
ENST00000679709.1:c.*1004T>C	ENSP00000506623.1:n.*1004T>C
ENST00000679976.1:c.*625T>C	ENSP00000505565.1:n.*625T>C
ENST00000680166.1:n.4330T>C
ENST00000680315.1:n.924T>C
ENST00000680517.1:c.*429T>C	ENSP00000505803.1:n.*429T>C
ENST00000680582.1:n.2003T>C
ENST00000680613.1:c.*534T>C	ENSP00000506114.1:n.*534T>C
ENST00000680662.1:c.*955T>C	ENSP00000505080.1:n.*955T>C
ENST00000680691.1:c.*704T>C	ENSP00000506487.1:n.*704T>C
ENST00000680694.1:c.*629T>C	ENSP00000505658.1:n.*629T>C
ENST00000680743.1:c.*830T>C	ENSP00000505073.1:n.*830T>C
ENST00000680749.1:c.*326T>C	ENSP00000505122.1:n.*326T>C
ENST00000680798.1:c.*516T>C	ENSP00000505670.1:n.*516T>C
ENST00000680805.1:c.900T>C	ENSP00000505447.1:p.Gly300=
ENST00000680844.1:c.*825T>C	ENSP00000506541.1:n.*825T>C
ENST00000680948.1:c.*908T>C	ENSP00000505441.1:n.*908T>C
ENST00000680964.1:c.*134T>C	ENSP00000505961.1:n.*134T>C
ENST00000681037.1:c.*2525T>C	ENSP00000506025.1:n.*2525T>C
ENST00000681063.1:c.*310T>C	ENSP00000506616.1:n.*310T>C
ENST00000681209.1:c.*696T>C	ENSP00000505877.1:n.*696T>C
ENST00000681278.1:n.1743T>C
ENST00000681289.1:n.5036T>C
ENST00000681361.1:c.*708T>C	ENSP00000506679.1:n.*708T>C
ENST00000681430.1:c.*134T>C	ENSP00000506301.1:n.*134T>C
ENST00000681446.1:c.*745T>C	ENSP00000506244.1:n.*745T>C
ENST00000681450.1:c.*712T>C	ENSP00000505660.1:n.*712T>C
ENST00000681548.1:c.*627T>C	ENSP00000505275.1:n.*627T>C
ENST00000681616.1:c.*700T>C	ENSP00000505111.1:n.*700T>C
ENST00000681621.1:c.*625T>C	ENSP00000505770.1:n.*625T>C
ENST00000681680.1:n.3136T>C
ENST00000681720.1:c.*496T>C	ENSP00000505438.1:n.*496T>C
ENST00000681730.1:n.1263T>C
ENST00000681790.1:c.783T>C	ENSP00000505130.1:p.Gly261=
ENST00000681837.1:n.1657T>C
ENST00000681913.1:n.3287T>C
ENST00000681916.1:c.*809T>C	ENSP00000506477.1:n.*809T>C
ENST00000681930.1:n.3165T>C
ENST00000370834.9:c.1140T>C	ENSP00000359871.5:p.Gly380=
ENST00000370841.8:c.1041T>C	ENSP00000359878.4:p.Gly347=
ENST00000420607.6:c.1053T>C	ENSP00000409612.2:p.Gly351=
ENST00000481374.1:n.314T>C
ENST00000525808.5:c.*627T>C	ENSP00000434823.1:n.*627T>C
ENST00000526129.5:c.*825T>C	ENSP00000434092.1:n.*825T>C
ENST00000526196.5:c.*809T>C	ENSP00000431953.1:n.*809T>C
ENST00000528016.1:c.160-7960T>C	ENSP00000434284.1:n.160-7960T>C
ENST00000529059.5:n.950T>C
ENST00000534334.5:c.*782T>C	ENSP00000435584.1:n.*782T>C
ENST00000541113.5:c.933T>C	ENSP00000442324.1:p.Gly311=
NM_000016.5:c.1041T>C	NP_000007.1:p.Gly347=
NM_001127328.2:c.1053T>C	NP_001120800.1:p.Gly351=
NM_001286042.1:c.933T>C	NP_001272971.1:p.Gly311=
NM_001286043.1:c.1140T>C	NP_001272972.1:p.Gly380=
NM_001286044.1:c.474T>C	NP_001272973.1:p.Gly158=
NM_000016.6:c.1041T>C MANE Select	NP_000007.1:p.Gly347=
NM_001127328.3:c.1053T>C	NP_001120800.1:p.Gly351=
NM_001286042.2:c.933T>C	NP_001272971.1:p.Gly311=
NM_001286043.2:c.1140T>C	NP_001272972.1:p.Gly380=
NM_001286044.2:c.474T>C	NP_001272973.1:p.Gly158=