Canonical Allele Identifier: CA1176720013

Gene: ACADM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75745797A= , CM000663.2:g.75745797A=	GRCh38
NC_000001.10:g.76211482A= , CM000663.1:g.76211482A=	GRCh37
NC_000001.9:g.75984070A=	NCBI36
NG_007045.2:g.26440A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.600-9A= MANE Select	ENSP00000359878.5:n.600-9A=
ENST00000473018.3:n.2724-9A=
ENST00000532207.6:n.1480A=
ENST00000541113.6:c.600-9A=	ENSP00000442324.2:n.600-9A=
ENST00000679509.1:n.1562-9A=
ENST00000679530.1:c.*368-9A=	ENSP00000506454.1:n.*368-9A=
ENST00000679615.1:n.2724-3622A=
ENST00000679687.1:c.162-9A=	ENSP00000506598.1:n.162-9A=
ENST00000679704.1:c.*366-9A=	ENSP00000505117.1:n.*366-9A=
ENST00000679709.1:c.*563-9A=	ENSP00000506623.1:n.*563-9A=
ENST00000679976.1:c.*184-9A=	ENSP00000505565.1:n.*184-9A=
ENST00000680166.1:n.3889-9A=
ENST00000680517.1:c.*97-3622A=	ENSP00000505803.1:n.*97-3622A=
ENST00000680582.1:n.1562-9A=
ENST00000680613.1:c.600-38A=	ENSP00000506114.1:n.600-38A=
ENST00000680662.1:c.*514-9A=	ENSP00000505080.1:n.*514-9A=
ENST00000680691.1:c.*263-9A=	ENSP00000506487.1:n.*263-9A=
ENST00000680694.1:c.*188-9A=	ENSP00000505658.1:n.*188-9A=
ENST00000680743.1:c.*267-9A=	ENSP00000505073.1:n.*267-9A=
ENST00000680749.1:c.600-3622A=	ENSP00000505122.1:n.600-3622A=
ENST00000680798.1:c.*184-3622A=	ENSP00000505670.1:n.*184-3622A=
ENST00000680805.1:c.600-9A=	ENSP00000505447.1:n.600-9A=
ENST00000680844.1:c.*384-9A=	ENSP00000506541.1:n.*384-9A=
ENST00000680948.1:c.*467-9A=	ENSP00000505441.1:n.*467-9A=
ENST00000680964.1:c.600-9A=	ENSP00000505961.1:n.600-9A=
ENST00000681037.1:c.*2113-38A=	ENSP00000506025.1:n.*2113-38A=
ENST00000681063.1:c.600-4654A=	ENSP00000506616.1:n.600-4654A=
ENST00000681209.1:c.*364-3622A=	ENSP00000505877.1:n.*364-3622A=
ENST00000681278.1:n.957-9A=
ENST00000681289.1:n.4586A=
ENST00000681361.1:c.*267-9A=	ENSP00000506679.1:n.*267-9A=
ENST00000681430.1:c.600-9A=	ENSP00000506301.1:n.600-9A=
ENST00000681446.1:c.*182-9A=	ENSP00000506244.1:n.*182-9A=
ENST00000681450.1:c.*271-9A=	ENSP00000505660.1:n.*271-9A=
ENST00000681548.1:c.*186-9A=	ENSP00000505275.1:n.*186-9A=
ENST00000681616.1:c.*368-3622A=	ENSP00000505111.1:n.*368-3622A=
ENST00000681621.1:c.*184-9A=	ENSP00000505770.1:n.*184-9A=
ENST00000681680.1:n.2724-38A=
ENST00000681720.1:c.*55-9A=	ENSP00000505438.1:n.*55-9A=
ENST00000681730.1:n.822-9A=
ENST00000681790.1:c.342-9A=	ENSP00000505130.1:n.342-9A=
ENST00000681837.1:n.1216-9A=
ENST00000681913.1:n.2724-9A=
ENST00000681916.1:c.*368-9A=	ENSP00000506477.1:n.*368-9A=
ENST00000681930.1:n.2724-9A=
ENST00000370834.9:c.699-9A=	ENSP00000359871.5:n.699-9A=
ENST00000370841.8:c.600-9A=	ENSP00000359878.4:n.600-9A=
ENST00000420607.6:c.612-9A=	ENSP00000409612.2:n.612-9A=
ENST00000525808.5:c.*186-9A=	ENSP00000434823.1:n.*186-9A=
ENST00000526129.5:c.*384-9A=	ENSP00000434092.1:n.*384-9A=
ENST00000526196.5:c.*368-9A=	ENSP00000431953.1:n.*368-9A=
ENST00000526930.1:n.373-9A=
ENST00000529059.5:n.509-9A=
ENST00000530953.6:c.*97-9A=	ENSP00000431372.1:n.*97-9A=
ENST00000532207.5:n.321A=
ENST00000532509.5:c.*364-9A=	ENSP00000432522.1:n.*364-9A=
ENST00000534334.5:c.*184-9A=	ENSP00000435584.1:n.*184-9A=
ENST00000541113.5:c.492-9A=	ENSP00000442324.1:n.492-9A=
NM_000016.5:c.600-9A=	NP_000007.1:n.600-9A=
NM_001127328.2:c.612-9A=	NP_001120800.1:n.612-9A=
NM_001286042.1:c.492-9A=	NP_001272971.1:n.492-9A=
NM_001286043.1:c.699-9A=	NP_001272972.1:n.699-9A=
NM_001286044.1:c.33-9A=	NP_001272973.1:n.33-9A=
NM_000016.6:c.600-9A= MANE Select	NP_000007.1:n.600-9A=
NM_001127328.3:c.612-9A=	NP_001120800.1:n.612-9A=
NM_001286042.2:c.492-9A=	NP_001272971.1:n.492-9A=
NM_001286043.2:c.699-9A=	NP_001272972.1:n.699-9A=
NM_001286044.2:c.33-9A=	NP_001272973.1:n.33-9A=