Canonical Allele Identifier: CA418707624

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226923T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761238T>A , CM000663.2:g.75761238T>A	GRCh38
NC_000001.10:g.76226923T>A , CM000663.1:g.76226923T>A	GRCh37
NC_000001.9:g.75999511T>A	NCBI36
NG_007045.2:g.41881T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.1062T>A MANE Select	ENSP00000359878.5:p.Ala354=
ENST00000473018.3:n.3186T>A
ENST00000532207.6:n.2073T>A
ENST00000541113.6:c.966T>A	ENSP00000442324.2:p.Ala322=
ENST00000679509.1:n.2024T>A
ENST00000679530.1:c.*830T>A	ENSP00000506454.1:n.*830T>A
ENST00000679615.1:n.3077T>A
ENST00000679687.1:c.624T>A	ENSP00000506598.1:p.Ala208=
ENST00000679704.1:c.*828T>A	ENSP00000505117.1:n.*828T>A
ENST00000679709.1:c.*1025T>A	ENSP00000506623.1:n.*1025T>A
ENST00000679976.1:c.*646T>A	ENSP00000505565.1:n.*646T>A
ENST00000680166.1:n.4351T>A
ENST00000680315.1:n.945T>A
ENST00000680517.1:c.*450T>A	ENSP00000505803.1:n.*450T>A
ENST00000680582.1:n.2024T>A
ENST00000680613.1:c.*555T>A	ENSP00000506114.1:n.*555T>A
ENST00000680662.1:c.*976T>A	ENSP00000505080.1:n.*976T>A
ENST00000680691.1:c.*725T>A	ENSP00000506487.1:n.*725T>A
ENST00000680694.1:c.*650T>A	ENSP00000505658.1:n.*650T>A
ENST00000680743.1:c.*851T>A	ENSP00000505073.1:n.*851T>A
ENST00000680749.1:c.*347T>A	ENSP00000505122.1:n.*347T>A
ENST00000680798.1:c.*537T>A	ENSP00000505670.1:n.*537T>A
ENST00000680805.1:c.921T>A	ENSP00000505447.1:p.Ala307=
ENST00000680844.1:c.*846T>A	ENSP00000506541.1:n.*846T>A
ENST00000680948.1:c.*929T>A	ENSP00000505441.1:n.*929T>A
ENST00000680964.1:c.*155T>A	ENSP00000505961.1:n.*155T>A
ENST00000681037.1:c.*2546T>A	ENSP00000506025.1:n.*2546T>A
ENST00000681063.1:c.*331T>A	ENSP00000506616.1:n.*331T>A
ENST00000681209.1:c.*717T>A	ENSP00000505877.1:n.*717T>A
ENST00000681278.1:n.1764T>A
ENST00000681289.1:n.5057T>A
ENST00000681361.1:c.*729T>A	ENSP00000506679.1:n.*729T>A
ENST00000681430.1:c.*155T>A	ENSP00000506301.1:n.*155T>A
ENST00000681446.1:c.*766T>A	ENSP00000506244.1:n.*766T>A
ENST00000681450.1:c.*733T>A	ENSP00000505660.1:n.*733T>A
ENST00000681548.1:c.*648T>A	ENSP00000505275.1:n.*648T>A
ENST00000681616.1:c.*721T>A	ENSP00000505111.1:n.*721T>A
ENST00000681621.1:c.*646T>A	ENSP00000505770.1:n.*646T>A
ENST00000681680.1:n.3157T>A
ENST00000681720.1:c.*517T>A	ENSP00000505438.1:n.*517T>A
ENST00000681730.1:n.1284T>A
ENST00000681790.1:c.804T>A	ENSP00000505130.1:p.Ala268=
ENST00000681837.1:n.1678T>A
ENST00000681913.1:n.3308T>A
ENST00000681916.1:c.*830T>A	ENSP00000506477.1:n.*830T>A
ENST00000681930.1:n.3186T>A
ENST00000370834.9:c.1161T>A	ENSP00000359871.5:p.Ala387=
ENST00000370841.8:c.1062T>A	ENSP00000359878.4:p.Ala354=
ENST00000420607.6:c.1074T>A	ENSP00000409612.2:p.Ala358=
ENST00000481374.1:n.335T>A
ENST00000525808.5:c.*648T>A	ENSP00000434823.1:n.*648T>A
ENST00000526129.5:c.*846T>A	ENSP00000434092.1:n.*846T>A
ENST00000526196.5:c.*830T>A	ENSP00000431953.1:n.*830T>A
ENST00000528016.1:c.160-7939T>A	ENSP00000434284.1:n.160-7939T>A
ENST00000529059.5:n.971T>A
ENST00000534334.5:c.*803T>A	ENSP00000435584.1:n.*803T>A
ENST00000541113.5:c.954T>A	ENSP00000442324.1:p.Ala318=
NM_000016.5:c.1062T>A	NP_000007.1:p.Ala354=
NM_001127328.2:c.1074T>A	NP_001120800.1:p.Ala358=
NM_001286042.1:c.954T>A	NP_001272971.1:p.Ala318=
NM_001286043.1:c.1161T>A	NP_001272972.1:p.Ala387=
NM_001286044.1:c.495T>A	NP_001272973.1:p.Ala165=
NM_000016.6:c.1062T>A MANE Select	NP_000007.1:p.Ala354=
NM_001127328.3:c.1074T>A	NP_001120800.1:p.Ala358=
NM_001286042.2:c.954T>A	NP_001272971.1:p.Ala318=
NM_001286043.2:c.1161T>A	NP_001272972.1:p.Ala387=
NM_001286044.2:c.495T>A	NP_001272973.1:p.Ala165=