Canonical Allele Identifier: CA418545008

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76216153T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75750468T>A , CM000663.2:g.75750468T>A	GRCh38
NC_000001.10:g.76216153T>A , CM000663.1:g.76216153T>A	GRCh37
NC_000001.9:g.75988741T>A	NCBI36
NG_007045.2:g.31111T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.867T>A MANE Select	ENSP00000359878.5:p.Val289=
ENST00000473018.3:n.2991T>A
ENST00000532207.6:n.1756T>A
ENST00000541113.6:c.849+909T>A	ENSP00000442324.2:n.849+909T>A
ENST00000679509.1:n.1829T>A
ENST00000679530.1:c.*635T>A	ENSP00000506454.1:n.*635T>A
ENST00000679615.1:n.2882T>A
ENST00000679687.1:c.429T>A	ENSP00000506598.1:p.Val143=
ENST00000679704.1:c.*633T>A	ENSP00000505117.1:n.*633T>A
ENST00000679709.1:c.*830T>A	ENSP00000506623.1:n.*830T>A
ENST00000679976.1:c.*451T>A	ENSP00000505565.1:n.*451T>A
ENST00000680166.1:n.4156T>A
ENST00000680315.1:n.750T>A
ENST00000680517.1:c.*255T>A	ENSP00000505803.1:n.*255T>A
ENST00000680582.1:n.1829T>A
ENST00000680613.1:c.*238T>A	ENSP00000506114.1:n.*238T>A
ENST00000680662.1:c.*781T>A	ENSP00000505080.1:n.*781T>A
ENST00000680691.1:c.*530T>A	ENSP00000506487.1:n.*530T>A
ENST00000680694.1:c.*455T>A	ENSP00000505658.1:n.*455T>A
ENST00000680743.1:c.*534T>A	ENSP00000505073.1:n.*534T>A
ENST00000680749.1:c.*152T>A	ENSP00000505122.1:n.*152T>A
ENST00000680798.1:c.*342T>A	ENSP00000505670.1:n.*342T>A
ENST00000680805.1:c.726T>A	ENSP00000505447.1:p.Val242=
ENST00000680844.1:c.*651T>A	ENSP00000506541.1:n.*651T>A
ENST00000680948.1:c.*734T>A	ENSP00000505441.1:n.*734T>A
ENST00000680964.1:c.867T>A	ENSP00000505961.1:p.Val289=
ENST00000681037.1:c.*2351T>A	ENSP00000506025.1:n.*2351T>A
ENST00000681063.1:c.*14T>A	ENSP00000506616.1:n.*14T>A
ENST00000681209.1:c.*522T>A	ENSP00000505877.1:n.*522T>A
ENST00000681278.1:n.1224T>A
ENST00000681289.1:n.4862T>A
ENST00000681361.1:c.*534T>A	ENSP00000506679.1:n.*534T>A
ENST00000681430.1:c.867T>A	ENSP00000506301.1:p.Val289=
ENST00000681446.1:c.*449T>A	ENSP00000506244.1:n.*449T>A
ENST00000681450.1:c.*538T>A	ENSP00000505660.1:n.*538T>A
ENST00000681548.1:c.*453T>A	ENSP00000505275.1:n.*453T>A
ENST00000681616.1:c.*526T>A	ENSP00000505111.1:n.*526T>A
ENST00000681621.1:c.*451T>A	ENSP00000505770.1:n.*451T>A
ENST00000681680.1:n.2962T>A
ENST00000681720.1:c.*322T>A	ENSP00000505438.1:n.*322T>A
ENST00000681730.1:n.1089T>A
ENST00000681790.1:c.609T>A	ENSP00000505130.1:p.Val203=
ENST00000681837.1:n.1483T>A
ENST00000681913.1:n.2991T>A
ENST00000681916.1:c.*635T>A	ENSP00000506477.1:n.*635T>A
ENST00000681930.1:n.2991T>A
ENST00000370834.9:c.966T>A	ENSP00000359871.5:p.Val322=
ENST00000370841.8:c.867T>A	ENSP00000359878.4:p.Val289=
ENST00000420607.6:c.879T>A	ENSP00000409612.2:p.Val293=
ENST00000481374.1:n.18T>A
ENST00000525808.5:c.*453T>A	ENSP00000434823.1:n.*453T>A
ENST00000526129.5:c.*651T>A	ENSP00000434092.1:n.*651T>A
ENST00000526196.5:c.*635T>A	ENSP00000431953.1:n.*635T>A
ENST00000528016.1:c.81T>A	ENSP00000434284.1:p.Val27=
ENST00000529059.5:n.776T>A
ENST00000532207.5:n.597T>A
ENST00000534334.5:c.*451T>A	ENSP00000435584.1:n.*451T>A
ENST00000541113.5:c.759T>A	ENSP00000442324.1:p.Val253=
NM_000016.5:c.867T>A	NP_000007.1:p.Val289=
NM_001127328.2:c.879T>A	NP_001120800.1:p.Val293=
NM_001286042.1:c.759T>A	NP_001272971.1:p.Val253=
NM_001286043.1:c.966T>A	NP_001272972.1:p.Val322=
NM_001286044.1:c.300T>A	NP_001272973.1:p.Val100=
NM_000016.6:c.867T>A MANE Select	NP_000007.1:p.Val289=
NM_001127328.3:c.879T>A	NP_001120800.1:p.Val293=
NM_001286042.2:c.759T>A	NP_001272971.1:p.Val253=
NM_001286043.2:c.966T>A	NP_001272972.1:p.Val322=
NM_001286044.2:c.300T>A	NP_001272973.1:p.Val100=