Canonical Allele Identifier: CA418707679

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226956A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761271A>C , CM000663.2:g.75761271A>C	GRCh38
NC_000001.10:g.76226956A>C , CM000663.1:g.76226956A>C	GRCh37
NC_000001.9:g.75999544A>C	NCBI36
NG_007045.2:g.41914A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.1095A>C MANE Select	ENSP00000359878.5:p.Ala365=
ENST00000473018.3:n.3219A>C
ENST00000532207.6:n.2106A>C
ENST00000541113.6:c.999A>C	ENSP00000442324.2:p.Ala333=
ENST00000679509.1:n.2057A>C
ENST00000679530.1:c.*863A>C	ENSP00000506454.1:n.*863A>C
ENST00000679615.1:n.3110A>C
ENST00000679687.1:c.657A>C	ENSP00000506598.1:p.Ala219=
ENST00000679704.1:c.*861A>C	ENSP00000505117.1:n.*861A>C
ENST00000679709.1:c.*1058A>C	ENSP00000506623.1:n.*1058A>C
ENST00000679976.1:c.*679A>C	ENSP00000505565.1:n.*679A>C
ENST00000680166.1:n.4384A>C
ENST00000680315.1:n.978A>C
ENST00000680517.1:c.*483A>C	ENSP00000505803.1:n.*483A>C
ENST00000680582.1:n.2057A>C
ENST00000680613.1:c.*588A>C	ENSP00000506114.1:n.*588A>C
ENST00000680662.1:c.*1009A>C	ENSP00000505080.1:n.*1009A>C
ENST00000680691.1:c.*758A>C	ENSP00000506487.1:n.*758A>C
ENST00000680694.1:c.*683A>C	ENSP00000505658.1:n.*683A>C
ENST00000680743.1:c.*884A>C	ENSP00000505073.1:n.*884A>C
ENST00000680749.1:c.*380A>C	ENSP00000505122.1:n.*380A>C
ENST00000680798.1:c.*570A>C	ENSP00000505670.1:n.*570A>C
ENST00000680805.1:c.954A>C	ENSP00000505447.1:p.Ala318=
ENST00000680844.1:c.*879A>C	ENSP00000506541.1:n.*879A>C
ENST00000680948.1:c.*962A>C	ENSP00000505441.1:n.*962A>C
ENST00000680964.1:c.*188A>C	ENSP00000505961.1:n.*188A>C
ENST00000681037.1:c.*2579A>C	ENSP00000506025.1:n.*2579A>C
ENST00000681063.1:c.*364A>C	ENSP00000506616.1:n.*364A>C
ENST00000681209.1:c.*750A>C	ENSP00000505877.1:n.*750A>C
ENST00000681278.1:n.1797A>C
ENST00000681289.1:n.5090A>C
ENST00000681361.1:c.*762A>C	ENSP00000506679.1:n.*762A>C
ENST00000681430.1:c.*188A>C	ENSP00000506301.1:n.*188A>C
ENST00000681446.1:c.*799A>C	ENSP00000506244.1:n.*799A>C
ENST00000681450.1:c.*766A>C	ENSP00000505660.1:n.*766A>C
ENST00000681548.1:c.*681A>C	ENSP00000505275.1:n.*681A>C
ENST00000681616.1:c.*754A>C	ENSP00000505111.1:n.*754A>C
ENST00000681621.1:c.*679A>C	ENSP00000505770.1:n.*679A>C
ENST00000681680.1:n.3190A>C
ENST00000681720.1:c.*550A>C	ENSP00000505438.1:n.*550A>C
ENST00000681730.1:n.1317A>C
ENST00000681790.1:c.837A>C	ENSP00000505130.1:p.Ala279=
ENST00000681837.1:n.1711A>C
ENST00000681913.1:n.3341A>C
ENST00000681916.1:c.*863A>C	ENSP00000506477.1:n.*863A>C
ENST00000681930.1:n.3219A>C
ENST00000370834.9:c.1194A>C	ENSP00000359871.5:p.Ala398=
ENST00000370841.8:c.1095A>C	ENSP00000359878.4:p.Ala365=
ENST00000420607.6:c.1107A>C	ENSP00000409612.2:p.Ala369=
ENST00000481374.1:n.368A>C
ENST00000525808.5:c.*681A>C	ENSP00000434823.1:n.*681A>C
ENST00000526129.5:c.*879A>C	ENSP00000434092.1:n.*879A>C
ENST00000526196.5:c.*863A>C	ENSP00000431953.1:n.*863A>C
ENST00000528016.1:c.160-7906A>C	ENSP00000434284.1:n.160-7906A>C
ENST00000529059.5:n.1004A>C
ENST00000541113.5:c.987A>C	ENSP00000442324.1:p.Ala329=
NM_000016.5:c.1095A>C	NP_000007.1:p.Ala365=
NM_001127328.2:c.1107A>C	NP_001120800.1:p.Ala369=
NM_001286042.1:c.987A>C	NP_001272971.1:p.Ala329=
NM_001286043.1:c.1194A>C	NP_001272972.1:p.Ala398=
NM_001286044.1:c.528A>C	NP_001272973.1:p.Ala176=
NM_000016.6:c.1095A>C MANE Select	NP_000007.1:p.Ala365=
NM_001127328.3:c.1107A>C	NP_001120800.1:p.Ala369=
NM_001286042.2:c.987A>C	NP_001272971.1:p.Ala329=
NM_001286043.2:c.1194A>C	NP_001272972.1:p.Ala398=
NM_001286044.2:c.528A>C	NP_001272973.1:p.Ala176=