Canonical Allele Identifier: CA913338

Gene: ACADM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75762802G>A , CM000663.2:g.75762802G>A	GRCh38
NC_000001.10:g.76228487G>A , CM000663.1:g.76228487G>A	GRCh37
NC_000001.9:g.76001075G>A	NCBI36
NG_007045.2:g.43445G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.*39G>A MANE Select	ENSP00000359878.5:n.*39G>A
ENST00000473018.3:n.3429G>A
ENST00000532207.6:n.3637G>A
ENST00000541113.6:c.*39G>A	ENSP00000442324.2:n.*39G>A
ENST00000679509.1:n.3588G>A
ENST00000679530.1:c.*1073G>A	ENSP00000506454.1:n.*1073G>A
ENST00000679615.1:n.4641G>A
ENST00000679687.1:c.*39G>A	ENSP00000506598.1:n.*39G>A
ENST00000679704.1:c.*1071G>A	ENSP00000505117.1:n.*1071G>A
ENST00000679709.1:c.*1268G>A	ENSP00000506623.1:n.*1268G>A
ENST00000679976.1:c.*889G>A	ENSP00000505565.1:n.*889G>A
ENST00000680166.1:n.4594G>A
ENST00000680582.1:n.2267G>A
ENST00000680613.1:c.*798G>A	ENSP00000506114.1:n.*798G>A
ENST00000680662.1:c.*1219G>A	ENSP00000505080.1:n.*1219G>A
ENST00000680691.1:c.*968G>A	ENSP00000506487.1:n.*968G>A
ENST00000680694.1:c.*893G>A	ENSP00000505658.1:n.*893G>A
ENST00000680743.1:c.*1094G>A	ENSP00000505073.1:n.*1094G>A
ENST00000680749.1:c.*590G>A	ENSP00000505122.1:n.*590G>A
ENST00000680798.1:c.*2101G>A	ENSP00000505670.1:n.*2101G>A
ENST00000680805.1:c.*39G>A	ENSP00000505447.1:n.*39G>A
ENST00000680844.1:c.*2410G>A	ENSP00000506541.1:n.*2410G>A
ENST00000680948.1:c.*1172G>A	ENSP00000505441.1:n.*1172G>A
ENST00000680964.1:c.*1719G>A	ENSP00000505961.1:n.*1719G>A
ENST00000681037.1:c.*2789G>A	ENSP00000506025.1:n.*2789G>A
ENST00000681063.1:c.*574G>A	ENSP00000506616.1:n.*574G>A
ENST00000681209.1:c.*960G>A	ENSP00000505877.1:n.*960G>A
ENST00000681278.1:n.2007G>A
ENST00000681289.1:n.5300G>A
ENST00000681361.1:c.*2293G>A	ENSP00000506679.1:n.*2293G>A
ENST00000681430.1:c.*398G>A	ENSP00000506301.1:n.*398G>A
ENST00000681446.1:c.*2330G>A	ENSP00000506244.1:n.*2330G>A
ENST00000681450.1:c.*976G>A	ENSP00000505660.1:n.*976G>A
ENST00000681548.1:c.*2212G>A	ENSP00000505275.1:n.*2212G>A
ENST00000681616.1:c.*2285G>A	ENSP00000505111.1:n.*2285G>A
ENST00000681621.1:c.*2210G>A	ENSP00000505770.1:n.*2210G>A
ENST00000681680.1:n.4721G>A
ENST00000681720.1:c.*760G>A	ENSP00000505438.1:n.*760G>A
ENST00000681730.1:n.1527G>A
ENST00000681790.1:c.*39G>A	ENSP00000505130.1:n.*39G>A
ENST00000681837.1:n.3242G>A
ENST00000681913.1:n.3551G>A
ENST00000681916.1:c.*1073G>A	ENSP00000506477.1:n.*1073G>A
ENST00000681930.1:n.4750G>A
ENST00000370834.9:c.*39G>A	ENSP00000359871.5:n.*39G>A
ENST00000370841.8:c.*39G>A	ENSP00000359878.4:n.*39G>A
ENST00000420607.6:c.*39G>A	ENSP00000409612.2:n.*39G>A
ENST00000481374.1:n.468-491G>A
ENST00000525808.5:c.*891G>A	ENSP00000434823.1:n.*891G>A
ENST00000526196.5:c.*1073G>A	ENSP00000431953.1:n.*1073G>A
ENST00000528016.1:c.160-6375G>A	ENSP00000434284.1:n.160-6375G>A
ENST00000529059.5:n.1214G>A
ENST00000541113.5:c.*39G>A	ENSP00000442324.1:n.*39G>A
NM_000016.5:c.*39G>A	NP_000007.1:n.*39G>A
NM_001127328.2:c.*39G>A	NP_001120800.1:n.*39G>A
NM_001286042.1:c.*39G>A	NP_001272971.1:n.*39G>A
NM_001286043.1:c.*39G>A	NP_001272972.1:n.*39G>A
NM_001286044.1:c.*39G>A	NP_001272973.1:n.*39G>A
NM_000016.6:c.*39G>A MANE Select	NP_000007.1:n.*39G>A
NM_001127328.3:c.*39G>A	NP_001120800.1:n.*39G>A
NM_001286042.2:c.*39G>A	NP_001272971.1:n.*39G>A
NM_001286043.2:c.*39G>A	NP_001272972.1:n.*39G>A
NM_001286044.2:c.*39G>A	NP_001272973.1:n.*39G>A