Canonical Allele Identifier: CA1176717810

Gene: ACADM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75732691G= , CM000663.2:g.75732691G=	GRCh38
NC_000001.10:g.76198376G= , CM000663.1:g.76198376G=	GRCh37
NC_000001.9:g.75970964G=	NCBI36
NG_007045.2:g.13334G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.166G= MANE Select	ENSP00000359878.5:p.Ala56=
ENST00000473018.3:n.523G=
ENST00000525881.6:n.523G=
ENST00000541113.6:c.166G=	ENSP00000442324.2:p.Ala56=
ENST00000679509.1:n.523G=
ENST00000679530.1:c.166G=	ENSP00000506454.1:p.Ala56=
ENST00000679615.1:n.523G=
ENST00000679687.1:c.31-7289G=	ENSP00000506598.1:n.31-7289G=
ENST00000679704.1:c.78G=	ENSP00000505117.1:p.Leu26=
ENST00000679709.1:c.*129G=	ENSP00000506623.1:n.*129G=
ENST00000679804.1:n.87G=
ENST00000679976.1:c.166G=	ENSP00000505565.1:p.Ala56=
ENST00000680166.1:n.1688G=
ENST00000680517.1:c.166G=	ENSP00000505803.1:p.Ala56=
ENST00000680582.1:n.523G=
ENST00000680613.1:c.166G=	ENSP00000506114.1:p.Ala56=
ENST00000680662.1:c.*80G=	ENSP00000505080.1:n.*80G=
ENST00000680691.1:c.166G=	ENSP00000506487.1:p.Ala56=
ENST00000680694.1:c.166G=	ENSP00000505658.1:p.Ala56=
ENST00000680743.1:c.78G=	ENSP00000505073.1:p.Leu26=
ENST00000680749.1:c.166G=	ENSP00000505122.1:p.Ala56=
ENST00000680798.1:c.166G=	ENSP00000505670.1:p.Ala56=
ENST00000680805.1:c.166G=	ENSP00000505447.1:p.Ala56=
ENST00000680844.1:c.78G=	ENSP00000506541.1:p.Leu26=
ENST00000680948.1:c.78G=	ENSP00000505441.1:p.Leu26=
ENST00000680964.1:c.166G=	ENSP00000505961.1:p.Ala56=
ENST00000681037.1:c.166G=	ENSP00000506025.1:p.Ala56=
ENST00000681063.1:c.166G=	ENSP00000506616.1:p.Ala56=
ENST00000681209.1:c.166G=	ENSP00000505877.1:p.Ala56=
ENST00000681278.1:n.523G=
ENST00000681289.1:n.523G=
ENST00000681361.1:c.78G=	ENSP00000506679.1:p.Leu26=
ENST00000681430.1:c.166G=	ENSP00000506301.1:p.Ala56=
ENST00000681446.1:c.166G=	ENSP00000506244.1:p.Ala56=
ENST00000681450.1:c.78G=	ENSP00000505660.1:p.Leu26=
ENST00000681548.1:c.78G=	ENSP00000505275.1:p.Leu26=
ENST00000681616.1:c.78G=	ENSP00000505111.1:p.Leu26=
ENST00000681621.1:c.166G=	ENSP00000505770.1:p.Ala56=
ENST00000681680.1:n.523G=
ENST00000681720.1:c.78G=	ENSP00000505438.1:p.Leu26=
ENST00000681730.1:n.388G=
ENST00000681790.1:c.-93G=	ENSP00000505130.1:n.-93G=
ENST00000681837.1:n.177G=
ENST00000681913.1:n.523G=
ENST00000681916.1:c.78G=	ENSP00000506477.1:p.Leu26=
ENST00000681930.1:n.523G=
ENST00000370834.9:c.166G=	ENSP00000359871.5:p.Ala56=
ENST00000370841.8:c.166G=	ENSP00000359878.4:p.Ala56=
ENST00000420607.6:c.178G=	ENSP00000409612.2:p.Ala60=
ENST00000473018.2:n.199G=
ENST00000525808.5:c.78G=	ENSP00000434823.1:p.Leu26=
ENST00000525881.5:n.175G=
ENST00000526129.5:c.166G=	ENSP00000434092.1:p.Ala56=
ENST00000526196.5:c.78G=	ENSP00000431953.1:p.Leu26=
ENST00000529059.5:n.176G=
ENST00000530953.6:c.118+4203G=	ENSP00000431372.1:n.118+4203G=
ENST00000532509.5:c.119-162G=	ENSP00000432522.1:n.119-162G=
ENST00000534146.5:n.245G=
ENST00000534334.5:c.166G=	ENSP00000435584.1:p.Ala56=
ENST00000541113.5:c.58G=	ENSP00000442324.1:p.Ala20=
NM_000016.5:c.166G=	NP_000007.1:p.Ala56=
NM_001127328.2:c.178G=	NP_001120800.1:p.Ala60=
NM_001286042.1:c.58G=	NP_001272971.1:p.Ala20=
NM_001286043.1:c.166G=	NP_001272972.1:p.Ala56=
NM_001286044.1:c.-220G=	NP_001272973.1:n.-220G=
NM_000016.6:c.166G= MANE Select	NP_000007.1:p.Ala56=
NM_001127328.3:c.178G=	NP_001120800.1:p.Ala60=
NM_001286042.2:c.58G=	NP_001272971.1:p.Ala20=
NM_001286043.2:c.166G=	NP_001272972.1:p.Ala56=
NM_001286044.2:c.-220G=	NP_001272973.1:n.-220G=