Canonical Allele Identifier: CA418544932

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76215220A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75749535A>T , CM000663.2:g.75749535A>T	GRCh38
NC_000001.10:g.76215220A>T , CM000663.1:g.76215220A>T	GRCh37
NC_000001.9:g.75987808A>T	NCBI36
NG_007045.2:g.30178A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.825A>T MANE Select	ENSP00000359878.5:p.Gly275=
ENST00000473018.3:n.2949A>T
ENST00000532207.6:n.1714A>T
ENST00000541113.6:c.825A>T	ENSP00000442324.2:p.Gly275=
ENST00000679509.1:n.1787A>T
ENST00000679530.1:c.*593A>T	ENSP00000506454.1:n.*593A>T
ENST00000679615.1:n.2840A>T
ENST00000679687.1:c.387A>T	ENSP00000506598.1:p.Gly129=
ENST00000679704.1:c.*591A>T	ENSP00000505117.1:n.*591A>T
ENST00000679709.1:c.*788A>T	ENSP00000506623.1:n.*788A>T
ENST00000679976.1:c.*409A>T	ENSP00000505565.1:n.*409A>T
ENST00000680166.1:n.4114A>T
ENST00000680517.1:c.*213A>T	ENSP00000505803.1:n.*213A>T
ENST00000680582.1:n.1787A>T
ENST00000680613.1:c.*196A>T	ENSP00000506114.1:n.*196A>T
ENST00000680662.1:c.*739A>T	ENSP00000505080.1:n.*739A>T
ENST00000680691.1:c.*488A>T	ENSP00000506487.1:n.*488A>T
ENST00000680694.1:c.*413A>T	ENSP00000505658.1:n.*413A>T
ENST00000680743.1:c.*492A>T	ENSP00000505073.1:n.*492A>T
ENST00000680749.1:c.*110A>T	ENSP00000505122.1:n.*110A>T
ENST00000680798.1:c.*300A>T	ENSP00000505670.1:n.*300A>T
ENST00000680805.1:c.709-916A>T	ENSP00000505447.1:n.709-916A>T
ENST00000680844.1:c.*609A>T	ENSP00000506541.1:n.*609A>T
ENST00000680948.1:c.*692A>T	ENSP00000505441.1:n.*692A>T
ENST00000680964.1:c.825A>T	ENSP00000505961.1:p.Gly275=
ENST00000681037.1:c.*2309A>T	ENSP00000506025.1:n.*2309A>T
ENST00000681063.1:c.600-916A>T	ENSP00000506616.1:n.600-916A>T
ENST00000681209.1:c.*480A>T	ENSP00000505877.1:n.*480A>T
ENST00000681278.1:n.1182A>T
ENST00000681289.1:n.4820A>T
ENST00000681361.1:c.*492A>T	ENSP00000506679.1:n.*492A>T
ENST00000681430.1:c.825A>T	ENSP00000506301.1:p.Gly275=
ENST00000681446.1:c.*407A>T	ENSP00000506244.1:n.*407A>T
ENST00000681450.1:c.*496A>T	ENSP00000505660.1:n.*496A>T
ENST00000681548.1:c.*411A>T	ENSP00000505275.1:n.*411A>T
ENST00000681616.1:c.*484A>T	ENSP00000505111.1:n.*484A>T
ENST00000681621.1:c.*409A>T	ENSP00000505770.1:n.*409A>T
ENST00000681680.1:n.2920A>T
ENST00000681720.1:c.*280A>T	ENSP00000505438.1:n.*280A>T
ENST00000681730.1:n.1047A>T
ENST00000681790.1:c.567A>T	ENSP00000505130.1:p.Gly189=
ENST00000681837.1:n.1441A>T
ENST00000681913.1:n.2949A>T
ENST00000681916.1:c.*593A>T	ENSP00000506477.1:n.*593A>T
ENST00000681930.1:n.2949A>T
ENST00000370834.9:c.924A>T	ENSP00000359871.5:p.Gly308=
ENST00000370841.8:c.825A>T	ENSP00000359878.4:p.Gly275=
ENST00000420607.6:c.837A>T	ENSP00000409612.2:p.Gly279=
ENST00000525808.5:c.*411A>T	ENSP00000434823.1:n.*411A>T
ENST00000526129.5:c.*609A>T	ENSP00000434092.1:n.*609A>T
ENST00000526196.5:c.*593A>T	ENSP00000431953.1:n.*593A>T
ENST00000528016.1:c.39A>T	ENSP00000434284.1:p.Gly13=
ENST00000529059.5:n.734A>T
ENST00000530953.6:c.*322A>T	ENSP00000431372.1:n.*322A>T
ENST00000532207.5:n.555A>T
ENST00000532509.5:c.*589A>T	ENSP00000432522.1:n.*589A>T
ENST00000534334.5:c.*409A>T	ENSP00000435584.1:n.*409A>T
ENST00000541113.5:c.717A>T	ENSP00000442324.1:p.Gly239=
NM_000016.5:c.825A>T	NP_000007.1:p.Gly275=
NM_001127328.2:c.837A>T	NP_001120800.1:p.Gly279=
NM_001286042.1:c.717A>T	NP_001272971.1:p.Gly239=
NM_001286043.1:c.924A>T	NP_001272972.1:p.Gly308=
NM_001286044.1:c.258A>T	NP_001272973.1:p.Gly86=
NM_000016.6:c.825A>T MANE Select	NP_000007.1:p.Gly275=
NM_001127328.3:c.837A>T	NP_001120800.1:p.Gly279=
NM_001286042.2:c.717A>T	NP_001272971.1:p.Gly239=
NM_001286043.2:c.924A>T	NP_001272972.1:p.Gly308=
NM_001286044.2:c.258A>T	NP_001272973.1:p.Gly86=