Canonical Allele Identifier: CA10576247

Gene: ACADM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75762840C>T , CM000663.2:g.75762840C>T	GRCh38
NC_000001.10:g.76228525C>T , CM000663.1:g.76228525C>T	GRCh37
NC_000001.9:g.76001113C>T	NCBI36
NG_007045.2:g.43483C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.*77C>T MANE Select	ENSP00000359878.5:n.*77C>T
ENST00000473018.3:n.3467C>T
ENST00000532207.6:n.3675C>T
ENST00000541113.6:c.*77C>T	ENSP00000442324.2:n.*77C>T
ENST00000679509.1:n.3626C>T
ENST00000679530.1:c.*1111C>T	ENSP00000506454.1:n.*1111C>T
ENST00000679615.1:n.4679C>T
ENST00000679687.1:c.*77C>T	ENSP00000506598.1:n.*77C>T
ENST00000679704.1:c.*1109C>T	ENSP00000505117.1:n.*1109C>T
ENST00000679709.1:c.*1306C>T	ENSP00000506623.1:n.*1306C>T
ENST00000679976.1:c.*927C>T	ENSP00000505565.1:n.*927C>T
ENST00000680166.1:n.4632C>T
ENST00000680582.1:n.2305C>T
ENST00000680613.1:c.*836C>T	ENSP00000506114.1:n.*836C>T
ENST00000680662.1:c.*1257C>T	ENSP00000505080.1:n.*1257C>T
ENST00000680691.1:c.*1006C>T	ENSP00000506487.1:n.*1006C>T
ENST00000680694.1:c.*931C>T	ENSP00000505658.1:n.*931C>T
ENST00000680743.1:c.*1132C>T	ENSP00000505073.1:n.*1132C>T
ENST00000680749.1:c.*628C>T	ENSP00000505122.1:n.*628C>T
ENST00000680798.1:c.*2139C>T	ENSP00000505670.1:n.*2139C>T
ENST00000680805.1:c.*77C>T	ENSP00000505447.1:n.*77C>T
ENST00000680844.1:c.*2448C>T	ENSP00000506541.1:n.*2448C>T
ENST00000680948.1:c.*1210C>T	ENSP00000505441.1:n.*1210C>T
ENST00000680964.1:c.*1757C>T	ENSP00000505961.1:n.*1757C>T
ENST00000681037.1:c.*2827C>T	ENSP00000506025.1:n.*2827C>T
ENST00000681063.1:c.*612C>T	ENSP00000506616.1:n.*612C>T
ENST00000681209.1:c.*998C>T	ENSP00000505877.1:n.*998C>T
ENST00000681278.1:n.2045C>T
ENST00000681289.1:n.5338C>T
ENST00000681361.1:c.*2331C>T	ENSP00000506679.1:n.*2331C>T
ENST00000681430.1:c.*436C>T	ENSP00000506301.1:n.*436C>T
ENST00000681446.1:c.*2368C>T	ENSP00000506244.1:n.*2368C>T
ENST00000681450.1:c.*1014C>T	ENSP00000505660.1:n.*1014C>T
ENST00000681548.1:c.*2250C>T	ENSP00000505275.1:n.*2250C>T
ENST00000681616.1:c.*2323C>T	ENSP00000505111.1:n.*2323C>T
ENST00000681621.1:c.*2248C>T	ENSP00000505770.1:n.*2248C>T
ENST00000681680.1:n.4759C>T
ENST00000681720.1:c.*798C>T	ENSP00000505438.1:n.*798C>T
ENST00000681730.1:n.1565C>T
ENST00000681790.1:c.*77C>T	ENSP00000505130.1:n.*77C>T
ENST00000681837.1:n.3280C>T
ENST00000681913.1:n.3589C>T
ENST00000681916.1:c.*1111C>T	ENSP00000506477.1:n.*1111C>T
ENST00000681930.1:n.4788C>T
ENST00000370834.9:c.*77C>T	ENSP00000359871.5:n.*77C>T
ENST00000370841.8:c.*77C>T	ENSP00000359878.4:n.*77C>T
ENST00000481374.1:n.468-453C>T
ENST00000525808.5:c.*929C>T	ENSP00000434823.1:n.*929C>T
ENST00000526196.5:c.*1111C>T	ENSP00000431953.1:n.*1111C>T
ENST00000528016.1:c.160-6337C>T	ENSP00000434284.1:n.160-6337C>T
ENST00000529059.5:n.1252C>T
ENST00000541113.5:c.*77C>T	ENSP00000442324.1:n.*77C>T
NM_000016.5:c.*77C>T	NP_000007.1:n.*77C>T
NM_001127328.2:c.*77C>T	NP_001120800.1:n.*77C>T
NM_001286042.1:c.*77C>T	NP_001272971.1:n.*77C>T
NM_001286043.1:c.*77C>T	NP_001272972.1:n.*77C>T
NM_001286044.1:c.*77C>T	NP_001272973.1:n.*77C>T
NM_000016.6:c.*77C>T MANE Select	NP_000007.1:n.*77C>T
NM_001127328.3:c.*77C>T	NP_001120800.1:n.*77C>T
NM_001286042.2:c.*77C>T	NP_001272971.1:n.*77C>T
NM_001286043.2:c.*77C>T	NP_001272972.1:n.*77C>T
NM_001286044.2:c.*77C>T	NP_001272973.1:n.*77C>T