Canonical Allele Identifier: CA418539889

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76205688A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75740003A>T , CM000663.2:g.75740003A>T	GRCh38
NC_000001.10:g.76205688A>T , CM000663.1:g.76205688A>T	GRCh37
NC_000001.9:g.75978276A>T	NCBI36
NG_007045.2:g.20646A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.492A>T MANE Select	ENSP00000359878.5:p.Gly164=
ENST00000473018.3:n.2616A>T
ENST00000541113.6:c.492A>T	ENSP00000442324.2:p.Gly164=
ENST00000679509.1:n.1454A>T
ENST00000679530.1:c.*260A>T	ENSP00000506454.1:n.*260A>T
ENST00000679615.1:n.2616A>T
ENST00000679687.1:c.54A>T	ENSP00000506598.1:p.Gly18=
ENST00000679704.1:c.*258A>T	ENSP00000505117.1:n.*258A>T
ENST00000679709.1:c.*455A>T	ENSP00000506623.1:n.*455A>T
ENST00000679804.1:n.231A>T
ENST00000679976.1:c.*76A>T	ENSP00000505565.1:n.*76A>T
ENST00000680166.1:n.3781A>T
ENST00000680517.1:c.310A>T	ENSP00000505803.1:p.Ser104Cys
ENST00000680582.1:n.1454A>T
ENST00000680613.1:c.492A>T	ENSP00000506114.1:p.Gly164=
ENST00000680662.1:c.*406A>T	ENSP00000505080.1:n.*406A>T
ENST00000680691.1:c.*155A>T	ENSP00000506487.1:n.*155A>T
ENST00000680694.1:c.*80A>T	ENSP00000505658.1:n.*80A>T
ENST00000680743.1:c.*159A>T	ENSP00000505073.1:n.*159A>T
ENST00000680749.1:c.492A>T	ENSP00000505122.1:p.Gly164=
ENST00000680798.1:c.*76A>T	ENSP00000505670.1:n.*76A>T
ENST00000680805.1:c.492A>T	ENSP00000505447.1:p.Gly164=
ENST00000680844.1:c.*276A>T	ENSP00000506541.1:n.*276A>T
ENST00000680948.1:c.*359A>T	ENSP00000505441.1:n.*359A>T
ENST00000680964.1:c.492A>T	ENSP00000505961.1:p.Gly164=
ENST00000681037.1:c.492A>T	ENSP00000506025.1:p.Gly164=
ENST00000681063.1:c.492A>T	ENSP00000506616.1:p.Gly164=
ENST00000681209.1:c.*256A>T	ENSP00000505877.1:n.*256A>T
ENST00000681278.1:n.849A>T
ENST00000681289.1:n.849A>T
ENST00000681361.1:c.*159A>T	ENSP00000506679.1:n.*159A>T
ENST00000681430.1:c.492A>T	ENSP00000506301.1:p.Gly164=
ENST00000681446.1:c.*74A>T	ENSP00000506244.1:n.*74A>T
ENST00000681450.1:c.*163A>T	ENSP00000505660.1:n.*163A>T
ENST00000681548.1:c.*78A>T	ENSP00000505275.1:n.*78A>T
ENST00000681616.1:c.*260A>T	ENSP00000505111.1:n.*260A>T
ENST00000681621.1:c.*76A>T	ENSP00000505770.1:n.*76A>T
ENST00000681680.1:n.2616A>T
ENST00000681720.1:c.*55-5803A>T	ENSP00000505438.1:n.*55-5803A>T
ENST00000681730.1:n.714A>T
ENST00000681790.1:c.234A>T	ENSP00000505130.1:p.Gly78=
ENST00000681837.1:n.1108A>T
ENST00000681913.1:n.2616A>T
ENST00000681916.1:c.*260A>T	ENSP00000506477.1:n.*260A>T
ENST00000681930.1:n.2616A>T
ENST00000370834.9:c.591A>T	ENSP00000359871.5:p.Gly197=
ENST00000370841.8:c.492A>T	ENSP00000359878.4:p.Gly164=
ENST00000420607.6:c.504A>T	ENSP00000409612.2:p.Gly168=
ENST00000525808.5:c.*78A>T	ENSP00000434823.1:n.*78A>T
ENST00000526129.5:c.*276A>T	ENSP00000434092.1:n.*276A>T
ENST00000526196.5:c.*260A>T	ENSP00000431953.1:n.*260A>T
ENST00000526930.1:n.265A>T
ENST00000529059.5:n.401A>T
ENST00000530953.6:c.142A>T	ENSP00000431372.1:p.Ser48Cys
ENST00000532509.5:c.*256A>T	ENSP00000432522.1:n.*256A>T
ENST00000534334.5:c.*76A>T	ENSP00000435584.1:n.*76A>T
ENST00000541113.5:c.384A>T	ENSP00000442324.1:p.Gly128=
NM_000016.5:c.492A>T	NP_000007.1:p.Gly164=
NM_001127328.2:c.504A>T	NP_001120800.1:p.Gly168=
NM_001286042.1:c.384A>T	NP_001272971.1:p.Gly128=
NM_001286043.1:c.591A>T	NP_001272972.1:p.Gly197=
NM_001286044.1:c.-76A>T	NP_001272973.1:n.-76A>T
NM_000016.6:c.492A>T MANE Select	NP_000007.1:p.Gly164=
NM_001127328.3:c.504A>T	NP_001120800.1:p.Gly168=
NM_001286042.2:c.384A>T	NP_001272971.1:p.Gly128=
NM_001286043.2:c.591A>T	NP_001272972.1:p.Gly197=
NM_001286044.2:c.-76A>T	NP_001272973.1:n.-76A>T