Canonical Allele Identifier: CA418545013

Gene: ACADM

Linked Data

• dbSNP Id: rs1557458445
• MyVariant Identifiers: chr1:g.76216156A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75750471A>T , CM000663.2:g.75750471A>T	GRCh38
NC_000001.10:g.76216156A>T , CM000663.1:g.76216156A>T	GRCh37
NC_000001.9:g.75988744A>T	NCBI36
NG_007045.2:g.31114A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.870A>T MANE Select	ENSP00000359878.5:p.Gly290=
ENST00000473018.3:n.2994A>T
ENST00000532207.6:n.1759A>T
ENST00000541113.6:c.849+912A>T	ENSP00000442324.2:n.849+912A>T
ENST00000679509.1:n.1832A>T
ENST00000679530.1:c.*638A>T	ENSP00000506454.1:n.*638A>T
ENST00000679615.1:n.2885A>T
ENST00000679687.1:c.432A>T	ENSP00000506598.1:p.Gly144=
ENST00000679704.1:c.*636A>T	ENSP00000505117.1:n.*636A>T
ENST00000679709.1:c.*833A>T	ENSP00000506623.1:n.*833A>T
ENST00000679976.1:c.*454A>T	ENSP00000505565.1:n.*454A>T
ENST00000680166.1:n.4159A>T
ENST00000680315.1:n.753A>T
ENST00000680517.1:c.*258A>T	ENSP00000505803.1:n.*258A>T
ENST00000680582.1:n.1832A>T
ENST00000680613.1:c.*241A>T	ENSP00000506114.1:n.*241A>T
ENST00000680662.1:c.*784A>T	ENSP00000505080.1:n.*784A>T
ENST00000680691.1:c.*533A>T	ENSP00000506487.1:n.*533A>T
ENST00000680694.1:c.*458A>T	ENSP00000505658.1:n.*458A>T
ENST00000680743.1:c.*537A>T	ENSP00000505073.1:n.*537A>T
ENST00000680749.1:c.*155A>T	ENSP00000505122.1:n.*155A>T
ENST00000680798.1:c.*345A>T	ENSP00000505670.1:n.*345A>T
ENST00000680805.1:c.729A>T	ENSP00000505447.1:p.Gly243=
ENST00000680844.1:c.*654A>T	ENSP00000506541.1:n.*654A>T
ENST00000680948.1:c.*737A>T	ENSP00000505441.1:n.*737A>T
ENST00000680964.1:c.870A>T	ENSP00000505961.1:p.Gly290=
ENST00000681037.1:c.*2354A>T	ENSP00000506025.1:n.*2354A>T
ENST00000681063.1:c.*17A>T	ENSP00000506616.1:n.*17A>T
ENST00000681209.1:c.*525A>T	ENSP00000505877.1:n.*525A>T
ENST00000681278.1:n.1227A>T
ENST00000681289.1:n.4865A>T
ENST00000681361.1:c.*537A>T	ENSP00000506679.1:n.*537A>T
ENST00000681430.1:c.870A>T	ENSP00000506301.1:p.Gly290=
ENST00000681446.1:c.*452A>T	ENSP00000506244.1:n.*452A>T
ENST00000681450.1:c.*541A>T	ENSP00000505660.1:n.*541A>T
ENST00000681548.1:c.*456A>T	ENSP00000505275.1:n.*456A>T
ENST00000681616.1:c.*529A>T	ENSP00000505111.1:n.*529A>T
ENST00000681621.1:c.*454A>T	ENSP00000505770.1:n.*454A>T
ENST00000681680.1:n.2965A>T
ENST00000681720.1:c.*325A>T	ENSP00000505438.1:n.*325A>T
ENST00000681730.1:n.1092A>T
ENST00000681790.1:c.612A>T	ENSP00000505130.1:p.Gly204=
ENST00000681837.1:n.1486A>T
ENST00000681913.1:n.2994A>T
ENST00000681916.1:c.*638A>T	ENSP00000506477.1:n.*638A>T
ENST00000681930.1:n.2994A>T
ENST00000370834.9:c.969A>T	ENSP00000359871.5:p.Gly323=
ENST00000370841.8:c.870A>T	ENSP00000359878.4:p.Gly290=
ENST00000420607.6:c.882A>T	ENSP00000409612.2:p.Gly294=
ENST00000481374.1:n.21A>T
ENST00000525808.5:c.*456A>T	ENSP00000434823.1:n.*456A>T
ENST00000526129.5:c.*654A>T	ENSP00000434092.1:n.*654A>T
ENST00000526196.5:c.*638A>T	ENSP00000431953.1:n.*638A>T
ENST00000528016.1:c.84A>T	ENSP00000434284.1:p.Gly28=
ENST00000529059.5:n.779A>T
ENST00000532207.5:n.600A>T
ENST00000534334.5:c.*454A>T	ENSP00000435584.1:n.*454A>T
ENST00000541113.5:c.762A>T	ENSP00000442324.1:p.Gly254=
NM_000016.5:c.870A>T	NP_000007.1:p.Gly290=
NM_001127328.2:c.882A>T	NP_001120800.1:p.Gly294=
NM_001286042.1:c.762A>T	NP_001272971.1:p.Gly254=
NM_001286043.1:c.969A>T	NP_001272972.1:p.Gly323=
NM_001286044.1:c.303A>T	NP_001272973.1:p.Gly101=
NM_000016.6:c.870A>T MANE Select	NP_000007.1:p.Gly290=
NM_001127328.3:c.882A>T	NP_001120800.1:p.Gly294=
NM_001286042.2:c.762A>T	NP_001272971.1:p.Gly254=
NM_001286043.2:c.969A>T	NP_001272972.1:p.Gly323=
NM_001286044.2:c.303A>T	NP_001272973.1:p.Gly101=