Canonical Allele Identifier: CA1176721885

Gene: ACADM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75750549A= , CM000663.2:g.75750549A=	GRCh38
NC_000001.10:g.76216234A= , CM000663.1:g.76216234A=	GRCh37
NC_000001.9:g.75988822A=	NCBI36
NG_007045.2:g.31192A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.945+3A= MANE Select	ENSP00000359878.5:n.945+3A=
ENST00000473018.3:n.3069+3A=
ENST00000532207.6:n.1834+3A=
ENST00000541113.6:c.849+990A=	ENSP00000442324.2:n.849+990A=
ENST00000679509.1:n.1907+3A=
ENST00000679530.1:c.*713+3A=	ENSP00000506454.1:n.*713+3A=
ENST00000679615.1:n.2960+3A=
ENST00000679687.1:c.507+3A=	ENSP00000506598.1:n.507+3A=
ENST00000679704.1:c.*711+3A=	ENSP00000505117.1:n.*711+3A=
ENST00000679709.1:c.*908+3A=	ENSP00000506623.1:n.*908+3A=
ENST00000679976.1:c.*529+3A=	ENSP00000505565.1:n.*529+3A=
ENST00000680166.1:n.4234+3A=
ENST00000680315.1:n.828+3A=
ENST00000680517.1:c.*333+3A=	ENSP00000505803.1:n.*333+3A=
ENST00000680582.1:n.1907+3A=
ENST00000680613.1:c.*316+3A=	ENSP00000506114.1:n.*316+3A=
ENST00000680662.1:c.*859+3A=	ENSP00000505080.1:n.*859+3A=
ENST00000680691.1:c.*608+3A=	ENSP00000506487.1:n.*608+3A=
ENST00000680694.1:c.*533+3A=	ENSP00000505658.1:n.*533+3A=
ENST00000680743.1:c.*612+3A=	ENSP00000505073.1:n.*612+3A=
ENST00000680749.1:c.*230+3A=	ENSP00000505122.1:n.*230+3A=
ENST00000680798.1:c.*420+3A=	ENSP00000505670.1:n.*420+3A=
ENST00000680805.1:c.804+3A=	ENSP00000505447.1:n.804+3A=
ENST00000680844.1:c.*729+3A=	ENSP00000506541.1:n.*729+3A=
ENST00000680948.1:c.*812+3A=	ENSP00000505441.1:n.*812+3A=
ENST00000680964.1:c.945+3A=	ENSP00000505961.1:n.945+3A=
ENST00000681037.1:c.*2429+3A=	ENSP00000506025.1:n.*2429+3A=
ENST00000681063.1:c.*92+3A=	ENSP00000506616.1:n.*92+3A=
ENST00000681209.1:c.*600+3A=	ENSP00000505877.1:n.*600+3A=
ENST00000681278.1:n.1305A=
ENST00000681289.1:n.4940+3A=
ENST00000681361.1:c.*612+3A=	ENSP00000506679.1:n.*612+3A=
ENST00000681430.1:c.945+3A=	ENSP00000506301.1:n.945+3A=
ENST00000681446.1:c.*527+3A=	ENSP00000506244.1:n.*527+3A=
ENST00000681450.1:c.*616+3A=	ENSP00000505660.1:n.*616+3A=
ENST00000681548.1:c.*531+3A=	ENSP00000505275.1:n.*531+3A=
ENST00000681616.1:c.*604+3A=	ENSP00000505111.1:n.*604+3A=
ENST00000681621.1:c.*529+3A=	ENSP00000505770.1:n.*529+3A=
ENST00000681680.1:n.3040+3A=
ENST00000681720.1:c.*400+3A=	ENSP00000505438.1:n.*400+3A=
ENST00000681730.1:n.1167+3A=
ENST00000681790.1:c.687+3A=	ENSP00000505130.1:n.687+3A=
ENST00000681837.1:n.1561+3A=
ENST00000681913.1:n.3069+3A=
ENST00000681916.1:c.*713+3A=	ENSP00000506477.1:n.*713+3A=
ENST00000681930.1:n.3069+3A=
ENST00000370834.9:c.1044+3A=	ENSP00000359871.5:n.1044+3A=
ENST00000370841.8:c.945+3A=	ENSP00000359878.4:n.945+3A=
ENST00000420607.6:c.957+3A=	ENSP00000409612.2:n.957+3A=
ENST00000481374.1:n.96+3A=
ENST00000525808.5:c.*531+3A=	ENSP00000434823.1:n.*531+3A=
ENST00000526129.5:c.*729+3A=	ENSP00000434092.1:n.*729+3A=
ENST00000526196.5:c.*713+3A=	ENSP00000431953.1:n.*713+3A=
ENST00000528016.1:c.159+3A=	ENSP00000434284.1:n.159+3A=
ENST00000529059.5:n.854+3A=
ENST00000532207.5:n.675+3A=
ENST00000534334.5:c.*529+3A=	ENSP00000435584.1:n.*529+3A=
ENST00000541113.5:c.837+3A=	ENSP00000442324.1:n.837+3A=
NM_000016.5:c.945+3A=	NP_000007.1:n.945+3A=
NM_001127328.2:c.957+3A=	NP_001120800.1:n.957+3A=
NM_001286042.1:c.837+3A=	NP_001272971.1:n.837+3A=
NM_001286043.1:c.1044+3A=	NP_001272972.1:n.1044+3A=
NM_001286044.1:c.378+3A=	NP_001272973.1:n.378+3A=
NM_000016.6:c.945+3A= MANE Select	NP_000007.1:n.945+3A=
NM_001127328.3:c.957+3A=	NP_001120800.1:n.957+3A=
NM_001286042.2:c.837+3A=	NP_001272971.1:n.837+3A=
NM_001286043.2:c.1044+3A=	NP_001272972.1:n.1044+3A=
NM_001286044.2:c.378+3A=	NP_001272973.1:n.378+3A=