Canonical Allele Identifier: CA418707662

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226944T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761259T>G , CM000663.2:g.75761259T>G	GRCh38
NC_000001.10:g.76226944T>G , CM000663.1:g.76226944T>G	GRCh37
NC_000001.9:g.75999532T>G	NCBI36
NG_007045.2:g.41902T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.1083T>G MANE Select	ENSP00000359878.5:p.Ala361=
ENST00000473018.3:n.3207T>G
ENST00000532207.6:n.2094T>G
ENST00000541113.6:c.987T>G	ENSP00000442324.2:p.Ala329=
ENST00000679509.1:n.2045T>G
ENST00000679530.1:c.*851T>G	ENSP00000506454.1:n.*851T>G
ENST00000679615.1:n.3098T>G
ENST00000679687.1:c.645T>G	ENSP00000506598.1:p.Ala215=
ENST00000679704.1:c.*849T>G	ENSP00000505117.1:n.*849T>G
ENST00000679709.1:c.*1046T>G	ENSP00000506623.1:n.*1046T>G
ENST00000679976.1:c.*667T>G	ENSP00000505565.1:n.*667T>G
ENST00000680166.1:n.4372T>G
ENST00000680315.1:n.966T>G
ENST00000680517.1:c.*471T>G	ENSP00000505803.1:n.*471T>G
ENST00000680582.1:n.2045T>G
ENST00000680613.1:c.*576T>G	ENSP00000506114.1:n.*576T>G
ENST00000680662.1:c.*997T>G	ENSP00000505080.1:n.*997T>G
ENST00000680691.1:c.*746T>G	ENSP00000506487.1:n.*746T>G
ENST00000680694.1:c.*671T>G	ENSP00000505658.1:n.*671T>G
ENST00000680743.1:c.*872T>G	ENSP00000505073.1:n.*872T>G
ENST00000680749.1:c.*368T>G	ENSP00000505122.1:n.*368T>G
ENST00000680798.1:c.*558T>G	ENSP00000505670.1:n.*558T>G
ENST00000680805.1:c.942T>G	ENSP00000505447.1:p.Ala314=
ENST00000680844.1:c.*867T>G	ENSP00000506541.1:n.*867T>G
ENST00000680948.1:c.*950T>G	ENSP00000505441.1:n.*950T>G
ENST00000680964.1:c.*176T>G	ENSP00000505961.1:n.*176T>G
ENST00000681037.1:c.*2567T>G	ENSP00000506025.1:n.*2567T>G
ENST00000681063.1:c.*352T>G	ENSP00000506616.1:n.*352T>G
ENST00000681209.1:c.*738T>G	ENSP00000505877.1:n.*738T>G
ENST00000681278.1:n.1785T>G
ENST00000681289.1:n.5078T>G
ENST00000681361.1:c.*750T>G	ENSP00000506679.1:n.*750T>G
ENST00000681430.1:c.*176T>G	ENSP00000506301.1:n.*176T>G
ENST00000681446.1:c.*787T>G	ENSP00000506244.1:n.*787T>G
ENST00000681450.1:c.*754T>G	ENSP00000505660.1:n.*754T>G
ENST00000681548.1:c.*669T>G	ENSP00000505275.1:n.*669T>G
ENST00000681616.1:c.*742T>G	ENSP00000505111.1:n.*742T>G
ENST00000681621.1:c.*667T>G	ENSP00000505770.1:n.*667T>G
ENST00000681680.1:n.3178T>G
ENST00000681720.1:c.*538T>G	ENSP00000505438.1:n.*538T>G
ENST00000681730.1:n.1305T>G
ENST00000681790.1:c.825T>G	ENSP00000505130.1:p.Ala275=
ENST00000681837.1:n.1699T>G
ENST00000681913.1:n.3329T>G
ENST00000681916.1:c.*851T>G	ENSP00000506477.1:n.*851T>G
ENST00000681930.1:n.3207T>G
ENST00000370834.9:c.1182T>G	ENSP00000359871.5:p.Ala394=
ENST00000370841.8:c.1083T>G	ENSP00000359878.4:p.Ala361=
ENST00000420607.6:c.1095T>G	ENSP00000409612.2:p.Ala365=
ENST00000481374.1:n.356T>G
ENST00000525808.5:c.*669T>G	ENSP00000434823.1:n.*669T>G
ENST00000526129.5:c.*867T>G	ENSP00000434092.1:n.*867T>G
ENST00000526196.5:c.*851T>G	ENSP00000431953.1:n.*851T>G
ENST00000528016.1:c.160-7918T>G	ENSP00000434284.1:n.160-7918T>G
ENST00000529059.5:n.992T>G
ENST00000541113.5:c.975T>G	ENSP00000442324.1:p.Ala325=
NM_000016.5:c.1083T>G	NP_000007.1:p.Ala361=
NM_001127328.2:c.1095T>G	NP_001120800.1:p.Ala365=
NM_001286042.1:c.975T>G	NP_001272971.1:p.Ala325=
NM_001286043.1:c.1182T>G	NP_001272972.1:p.Ala394=
NM_001286044.1:c.516T>G	NP_001272973.1:p.Ala172=
NM_000016.6:c.1083T>G MANE Select	NP_000007.1:p.Ala361=
NM_001127328.3:c.1095T>G	NP_001120800.1:p.Ala365=
NM_001286042.2:c.975T>G	NP_001272971.1:p.Ala325=
NM_001286043.2:c.1182T>G	NP_001272972.1:p.Ala394=
NM_001286044.2:c.516T>G	NP_001272973.1:p.Ala172=