Canonical Allele Identifier: CA418530594

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226815A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761130A>T , CM000663.2:g.75761130A>T	GRCh38
NC_000001.10:g.76226815A>T , CM000663.1:g.76226815A>T	GRCh37
NC_000001.9:g.75999403A>T	NCBI36
NG_007045.2:g.41773A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.954A>T MANE Select	ENSP00000359878.5:p.Ala318=
ENST00000473018.3:n.3078A>T
ENST00000532207.6:n.1965A>T
ENST00000541113.6:c.858A>T	ENSP00000442324.2:p.Ala286=
ENST00000679509.1:n.1916A>T
ENST00000679530.1:c.*722A>T	ENSP00000506454.1:n.*722A>T
ENST00000679615.1:n.2969A>T
ENST00000679687.1:c.516A>T	ENSP00000506598.1:p.Ala172=
ENST00000679704.1:c.*720A>T	ENSP00000505117.1:n.*720A>T
ENST00000679709.1:c.*917A>T	ENSP00000506623.1:n.*917A>T
ENST00000679976.1:c.*538A>T	ENSP00000505565.1:n.*538A>T
ENST00000680166.1:n.4243A>T
ENST00000680315.1:n.837A>T
ENST00000680517.1:c.*342A>T	ENSP00000505803.1:n.*342A>T
ENST00000680582.1:n.1916A>T
ENST00000680613.1:c.*447A>T	ENSP00000506114.1:n.*447A>T
ENST00000680662.1:c.*868A>T	ENSP00000505080.1:n.*868A>T
ENST00000680691.1:c.*617A>T	ENSP00000506487.1:n.*617A>T
ENST00000680694.1:c.*542A>T	ENSP00000505658.1:n.*542A>T
ENST00000680743.1:c.*743A>T	ENSP00000505073.1:n.*743A>T
ENST00000680749.1:c.*239A>T	ENSP00000505122.1:n.*239A>T
ENST00000680798.1:c.*429A>T	ENSP00000505670.1:n.*429A>T
ENST00000680805.1:c.813A>T	ENSP00000505447.1:p.Ala271=
ENST00000680844.1:c.*738A>T	ENSP00000506541.1:n.*738A>T
ENST00000680948.1:c.*821A>T	ENSP00000505441.1:n.*821A>T
ENST00000680964.1:c.*47A>T	ENSP00000505961.1:n.*47A>T
ENST00000681037.1:c.*2438A>T	ENSP00000506025.1:n.*2438A>T
ENST00000681063.1:c.*223A>T	ENSP00000506616.1:n.*223A>T
ENST00000681209.1:c.*609A>T	ENSP00000505877.1:n.*609A>T
ENST00000681278.1:n.1656A>T
ENST00000681289.1:n.4949A>T
ENST00000681361.1:c.*621A>T	ENSP00000506679.1:n.*621A>T
ENST00000681430.1:c.*47A>T	ENSP00000506301.1:n.*47A>T
ENST00000681446.1:c.*658A>T	ENSP00000506244.1:n.*658A>T
ENST00000681450.1:c.*625A>T	ENSP00000505660.1:n.*625A>T
ENST00000681548.1:c.*540A>T	ENSP00000505275.1:n.*540A>T
ENST00000681616.1:c.*613A>T	ENSP00000505111.1:n.*613A>T
ENST00000681621.1:c.*538A>T	ENSP00000505770.1:n.*538A>T
ENST00000681680.1:n.3049A>T
ENST00000681720.1:c.*409A>T	ENSP00000505438.1:n.*409A>T
ENST00000681730.1:n.1176A>T
ENST00000681790.1:c.696A>T	ENSP00000505130.1:p.Ala232=
ENST00000681837.1:n.1570A>T
ENST00000681913.1:n.3200A>T
ENST00000681916.1:c.*722A>T	ENSP00000506477.1:n.*722A>T
ENST00000681930.1:n.3078A>T
ENST00000370834.9:c.1053A>T	ENSP00000359871.5:p.Ala351=
ENST00000370841.8:c.954A>T	ENSP00000359878.4:p.Ala318=
ENST00000420607.6:c.966A>T	ENSP00000409612.2:p.Ala322=
ENST00000481374.1:n.227A>T
ENST00000525808.5:c.*540A>T	ENSP00000434823.1:n.*540A>T
ENST00000526129.5:c.*738A>T	ENSP00000434092.1:n.*738A>T
ENST00000526196.5:c.*722A>T	ENSP00000431953.1:n.*722A>T
ENST00000528016.1:c.160-8047A>T	ENSP00000434284.1:n.160-8047A>T
ENST00000529059.5:n.863A>T
ENST00000532207.5:n.684A>T
ENST00000534334.5:c.*695A>T	ENSP00000435584.1:n.*695A>T
ENST00000541113.5:c.846A>T	ENSP00000442324.1:p.Ala282=
NM_000016.5:c.954A>T	NP_000007.1:p.Ala318=
NM_001127328.2:c.966A>T	NP_001120800.1:p.Ala322=
NM_001286042.1:c.846A>T	NP_001272971.1:p.Ala282=
NM_001286043.1:c.1053A>T	NP_001272972.1:p.Ala351=
NM_001286044.1:c.387A>T	NP_001272973.1:p.Ala129=
NM_000016.6:c.954A>T MANE Select	NP_000007.1:p.Ala318=
NM_001127328.3:c.966A>T	NP_001120800.1:p.Ala322=
NM_001286042.2:c.846A>T	NP_001272971.1:p.Ala282=
NM_001286043.2:c.1053A>T	NP_001272972.1:p.Ala351=
NM_001286044.2:c.387A>T	NP_001272973.1:p.Ala129=