Canonical Allele Identifier: CA418707771

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76227010A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761325A>T , CM000663.2:g.75761325A>T	GRCh38
NC_000001.10:g.76227010A>T , CM000663.1:g.76227010A>T	GRCh37
NC_000001.9:g.75999598A>T	NCBI36
NG_007045.2:g.41968A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.1149A>T MANE Select	ENSP00000359878.5:p.Thr383=
ENST00000473018.3:n.3273A>T
ENST00000532207.6:n.2160A>T
ENST00000541113.6:c.1053A>T	ENSP00000442324.2:p.Thr351=
ENST00000679509.1:n.2111A>T
ENST00000679530.1:c.*917A>T	ENSP00000506454.1:n.*917A>T
ENST00000679615.1:n.3164A>T
ENST00000679687.1:c.711A>T	ENSP00000506598.1:p.Thr237=
ENST00000679704.1:c.*915A>T	ENSP00000505117.1:n.*915A>T
ENST00000679709.1:c.*1112A>T	ENSP00000506623.1:n.*1112A>T
ENST00000679976.1:c.*733A>T	ENSP00000505565.1:n.*733A>T
ENST00000680166.1:n.4438A>T
ENST00000680315.1:n.1032A>T
ENST00000680517.1:c.*537A>T	ENSP00000505803.1:n.*537A>T
ENST00000680582.1:n.2111A>T
ENST00000680613.1:c.*642A>T	ENSP00000506114.1:n.*642A>T
ENST00000680662.1:c.*1063A>T	ENSP00000505080.1:n.*1063A>T
ENST00000680691.1:c.*812A>T	ENSP00000506487.1:n.*812A>T
ENST00000680694.1:c.*737A>T	ENSP00000505658.1:n.*737A>T
ENST00000680743.1:c.*938A>T	ENSP00000505073.1:n.*938A>T
ENST00000680749.1:c.*434A>T	ENSP00000505122.1:n.*434A>T
ENST00000680798.1:c.*624A>T	ENSP00000505670.1:n.*624A>T
ENST00000680805.1:c.1008A>T	ENSP00000505447.1:p.Thr336=
ENST00000680844.1:c.*933A>T	ENSP00000506541.1:n.*933A>T
ENST00000680948.1:c.*1016A>T	ENSP00000505441.1:n.*1016A>T
ENST00000680964.1:c.*242A>T	ENSP00000505961.1:n.*242A>T
ENST00000681037.1:c.*2633A>T	ENSP00000506025.1:n.*2633A>T
ENST00000681063.1:c.*418A>T	ENSP00000506616.1:n.*418A>T
ENST00000681209.1:c.*804A>T	ENSP00000505877.1:n.*804A>T
ENST00000681278.1:n.1851A>T
ENST00000681289.1:n.5144A>T
ENST00000681361.1:c.*816A>T	ENSP00000506679.1:n.*816A>T
ENST00000681430.1:c.*242A>T	ENSP00000506301.1:n.*242A>T
ENST00000681446.1:c.*853A>T	ENSP00000506244.1:n.*853A>T
ENST00000681450.1:c.*820A>T	ENSP00000505660.1:n.*820A>T
ENST00000681548.1:c.*735A>T	ENSP00000505275.1:n.*735A>T
ENST00000681616.1:c.*808A>T	ENSP00000505111.1:n.*808A>T
ENST00000681621.1:c.*733A>T	ENSP00000505770.1:n.*733A>T
ENST00000681680.1:n.3244A>T
ENST00000681720.1:c.*604A>T	ENSP00000505438.1:n.*604A>T
ENST00000681730.1:n.1371A>T
ENST00000681790.1:c.891A>T	ENSP00000505130.1:p.Thr297=
ENST00000681837.1:n.1765A>T
ENST00000681913.1:n.3395A>T
ENST00000681916.1:c.*917A>T	ENSP00000506477.1:n.*917A>T
ENST00000681930.1:n.3273A>T
ENST00000370834.9:c.1248A>T	ENSP00000359871.5:p.Thr416=
ENST00000370841.8:c.1149A>T	ENSP00000359878.4:p.Thr383=
ENST00000420607.6:c.1161A>T	ENSP00000409612.2:p.Thr387=
ENST00000481374.1:n.422A>T
ENST00000525808.5:c.*735A>T	ENSP00000434823.1:n.*735A>T
ENST00000526129.5:c.*933A>T	ENSP00000434092.1:n.*933A>T
ENST00000526196.5:c.*917A>T	ENSP00000431953.1:n.*917A>T
ENST00000528016.1:c.160-7852A>T	ENSP00000434284.1:n.160-7852A>T
ENST00000529059.5:n.1058A>T
ENST00000541113.5:c.1041A>T	ENSP00000442324.1:p.Thr347=
NM_000016.5:c.1149A>T	NP_000007.1:p.Thr383=
NM_001127328.2:c.1161A>T	NP_001120800.1:p.Thr387=
NM_001286042.1:c.1041A>T	NP_001272971.1:p.Thr347=
NM_001286043.1:c.1248A>T	NP_001272972.1:p.Thr416=
NM_001286044.1:c.582A>T	NP_001272973.1:p.Thr194=
NM_000016.6:c.1149A>T MANE Select	NP_000007.1:p.Thr383=
NM_001127328.3:c.1161A>T	NP_001120800.1:p.Thr387=
NM_001286042.2:c.1041A>T	NP_001272971.1:p.Thr347=
NM_001286043.2:c.1248A>T	NP_001272972.1:p.Thr416=
NM_001286044.2:c.582A>T	NP_001272973.1:p.Thr194=