Canonical Allele Identifier: CA418544965

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76215241T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75749556T>A , CM000663.2:g.75749556T>A	GRCh38
NC_000001.10:g.76215241T>A , CM000663.1:g.76215241T>A	GRCh37
NC_000001.9:g.75987829T>A	NCBI36
NG_007045.2:g.30199T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.846T>A MANE Select	ENSP00000359878.5:p.Pro282=
ENST00000473018.3:n.2970T>A
ENST00000532207.6:n.1735T>A
ENST00000541113.6:c.846T>A	ENSP00000442324.2:p.Pro282=
ENST00000679509.1:n.1808T>A
ENST00000679530.1:c.*614T>A	ENSP00000506454.1:n.*614T>A
ENST00000679615.1:n.2861T>A
ENST00000679687.1:c.408T>A	ENSP00000506598.1:p.Pro136=
ENST00000679704.1:c.*612T>A	ENSP00000505117.1:n.*612T>A
ENST00000679709.1:c.*809T>A	ENSP00000506623.1:n.*809T>A
ENST00000679976.1:c.*430T>A	ENSP00000505565.1:n.*430T>A
ENST00000680166.1:n.4135T>A
ENST00000680517.1:c.*234T>A	ENSP00000505803.1:n.*234T>A
ENST00000680582.1:n.1808T>A
ENST00000680613.1:c.*217T>A	ENSP00000506114.1:n.*217T>A
ENST00000680662.1:c.*760T>A	ENSP00000505080.1:n.*760T>A
ENST00000680691.1:c.*509T>A	ENSP00000506487.1:n.*509T>A
ENST00000680694.1:c.*434T>A	ENSP00000505658.1:n.*434T>A
ENST00000680743.1:c.*513T>A	ENSP00000505073.1:n.*513T>A
ENST00000680749.1:c.*131T>A	ENSP00000505122.1:n.*131T>A
ENST00000680798.1:c.*321T>A	ENSP00000505670.1:n.*321T>A
ENST00000680805.1:c.709-895T>A	ENSP00000505447.1:n.709-895T>A
ENST00000680844.1:c.*630T>A	ENSP00000506541.1:n.*630T>A
ENST00000680948.1:c.*713T>A	ENSP00000505441.1:n.*713T>A
ENST00000680964.1:c.846T>A	ENSP00000505961.1:p.Pro282=
ENST00000681037.1:c.*2330T>A	ENSP00000506025.1:n.*2330T>A
ENST00000681063.1:c.600-895T>A	ENSP00000506616.1:n.600-895T>A
ENST00000681209.1:c.*501T>A	ENSP00000505877.1:n.*501T>A
ENST00000681278.1:n.1203T>A
ENST00000681289.1:n.4841T>A
ENST00000681361.1:c.*513T>A	ENSP00000506679.1:n.*513T>A
ENST00000681430.1:c.846T>A	ENSP00000506301.1:p.Pro282=
ENST00000681446.1:c.*428T>A	ENSP00000506244.1:n.*428T>A
ENST00000681450.1:c.*517T>A	ENSP00000505660.1:n.*517T>A
ENST00000681548.1:c.*432T>A	ENSP00000505275.1:n.*432T>A
ENST00000681616.1:c.*505T>A	ENSP00000505111.1:n.*505T>A
ENST00000681621.1:c.*430T>A	ENSP00000505770.1:n.*430T>A
ENST00000681680.1:n.2941T>A
ENST00000681720.1:c.*301T>A	ENSP00000505438.1:n.*301T>A
ENST00000681730.1:n.1068T>A
ENST00000681790.1:c.588T>A	ENSP00000505130.1:p.Pro196=
ENST00000681837.1:n.1462T>A
ENST00000681913.1:n.2970T>A
ENST00000681916.1:c.*614T>A	ENSP00000506477.1:n.*614T>A
ENST00000681930.1:n.2970T>A
ENST00000370834.9:c.945T>A	ENSP00000359871.5:p.Pro315=
ENST00000370841.8:c.846T>A	ENSP00000359878.4:p.Pro282=
ENST00000420607.6:c.858T>A	ENSP00000409612.2:p.Pro286=
ENST00000525808.5:c.*432T>A	ENSP00000434823.1:n.*432T>A
ENST00000526129.5:c.*630T>A	ENSP00000434092.1:n.*630T>A
ENST00000526196.5:c.*614T>A	ENSP00000431953.1:n.*614T>A
ENST00000528016.1:c.60T>A	ENSP00000434284.1:p.Pro20=
ENST00000529059.5:n.755T>A
ENST00000532207.5:n.576T>A
ENST00000534334.5:c.*430T>A	ENSP00000435584.1:n.*430T>A
ENST00000541113.5:c.738T>A	ENSP00000442324.1:p.Pro246=
NM_000016.5:c.846T>A	NP_000007.1:p.Pro282=
NM_001127328.2:c.858T>A	NP_001120800.1:p.Pro286=
NM_001286042.1:c.738T>A	NP_001272971.1:p.Pro246=
NM_001286043.1:c.945T>A	NP_001272972.1:p.Pro315=
NM_001286044.1:c.279T>A	NP_001272973.1:p.Pro93=
NM_000016.6:c.846T>A MANE Select	NP_000007.1:p.Pro282=
NM_001127328.3:c.858T>A	NP_001120800.1:p.Pro286=
NM_001286042.2:c.738T>A	NP_001272971.1:p.Pro246=
NM_001286043.2:c.945T>A	NP_001272972.1:p.Pro315=
NM_001286044.2:c.279T>A	NP_001272973.1:p.Pro93=