Canonical Allele Identifier: CA418530705

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226833T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761148T>G , CM000663.2:g.75761148T>G	GRCh38
NC_000001.10:g.76226833T>G , CM000663.1:g.76226833T>G	GRCh37
NC_000001.9:g.75999421T>G	NCBI36
NG_007045.2:g.41791T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.972T>G MANE Select	ENSP00000359878.5:p.Ala324=
ENST00000473018.3:n.3096T>G
ENST00000532207.6:n.1983T>G
ENST00000541113.6:c.876T>G	ENSP00000442324.2:p.Ala292=
ENST00000679509.1:n.1934T>G
ENST00000679530.1:c.*740T>G	ENSP00000506454.1:n.*740T>G
ENST00000679615.1:n.2987T>G
ENST00000679687.1:c.534T>G	ENSP00000506598.1:p.Ala178=
ENST00000679704.1:c.*738T>G	ENSP00000505117.1:n.*738T>G
ENST00000679709.1:c.*935T>G	ENSP00000506623.1:n.*935T>G
ENST00000679976.1:c.*556T>G	ENSP00000505565.1:n.*556T>G
ENST00000680166.1:n.4261T>G
ENST00000680315.1:n.855T>G
ENST00000680517.1:c.*360T>G	ENSP00000505803.1:n.*360T>G
ENST00000680582.1:n.1934T>G
ENST00000680613.1:c.*465T>G	ENSP00000506114.1:n.*465T>G
ENST00000680662.1:c.*886T>G	ENSP00000505080.1:n.*886T>G
ENST00000680691.1:c.*635T>G	ENSP00000506487.1:n.*635T>G
ENST00000680694.1:c.*560T>G	ENSP00000505658.1:n.*560T>G
ENST00000680743.1:c.*761T>G	ENSP00000505073.1:n.*761T>G
ENST00000680749.1:c.*257T>G	ENSP00000505122.1:n.*257T>G
ENST00000680798.1:c.*447T>G	ENSP00000505670.1:n.*447T>G
ENST00000680805.1:c.831T>G	ENSP00000505447.1:p.Ala277=
ENST00000680844.1:c.*756T>G	ENSP00000506541.1:n.*756T>G
ENST00000680948.1:c.*839T>G	ENSP00000505441.1:n.*839T>G
ENST00000680964.1:c.*65T>G	ENSP00000505961.1:n.*65T>G
ENST00000681037.1:c.*2456T>G	ENSP00000506025.1:n.*2456T>G
ENST00000681063.1:c.*241T>G	ENSP00000506616.1:n.*241T>G
ENST00000681209.1:c.*627T>G	ENSP00000505877.1:n.*627T>G
ENST00000681278.1:n.1674T>G
ENST00000681289.1:n.4967T>G
ENST00000681361.1:c.*639T>G	ENSP00000506679.1:n.*639T>G
ENST00000681430.1:c.*65T>G	ENSP00000506301.1:n.*65T>G
ENST00000681446.1:c.*676T>G	ENSP00000506244.1:n.*676T>G
ENST00000681450.1:c.*643T>G	ENSP00000505660.1:n.*643T>G
ENST00000681548.1:c.*558T>G	ENSP00000505275.1:n.*558T>G
ENST00000681616.1:c.*631T>G	ENSP00000505111.1:n.*631T>G
ENST00000681621.1:c.*556T>G	ENSP00000505770.1:n.*556T>G
ENST00000681680.1:n.3067T>G
ENST00000681720.1:c.*427T>G	ENSP00000505438.1:n.*427T>G
ENST00000681730.1:n.1194T>G
ENST00000681790.1:c.714T>G	ENSP00000505130.1:p.Ala238=
ENST00000681837.1:n.1588T>G
ENST00000681913.1:n.3218T>G
ENST00000681916.1:c.*740T>G	ENSP00000506477.1:n.*740T>G
ENST00000681930.1:n.3096T>G
ENST00000370834.9:c.1071T>G	ENSP00000359871.5:p.Ala357=
ENST00000370841.8:c.972T>G	ENSP00000359878.4:p.Ala324=
ENST00000420607.6:c.984T>G	ENSP00000409612.2:p.Ala328=
ENST00000481374.1:n.245T>G
ENST00000525808.5:c.*558T>G	ENSP00000434823.1:n.*558T>G
ENST00000526129.5:c.*756T>G	ENSP00000434092.1:n.*756T>G
ENST00000526196.5:c.*740T>G	ENSP00000431953.1:n.*740T>G
ENST00000528016.1:c.160-8029T>G	ENSP00000434284.1:n.160-8029T>G
ENST00000529059.5:n.881T>G
ENST00000532207.5:n.702T>G
ENST00000534334.5:c.*713T>G	ENSP00000435584.1:n.*713T>G
ENST00000541113.5:c.864T>G	ENSP00000442324.1:p.Ala288=
NM_000016.5:c.972T>G	NP_000007.1:p.Ala324=
NM_001127328.2:c.984T>G	NP_001120800.1:p.Ala328=
NM_001286042.1:c.864T>G	NP_001272971.1:p.Ala288=
NM_001286043.1:c.1071T>G	NP_001272972.1:p.Ala357=
NM_001286044.1:c.405T>G	NP_001272973.1:p.Ala135=
NM_000016.6:c.972T>G MANE Select	NP_000007.1:p.Ala324=
NM_001127328.3:c.984T>G	NP_001120800.1:p.Ala328=
NM_001286042.2:c.864T>G	NP_001272971.1:p.Ala288=
NM_001286043.2:c.1071T>G	NP_001272972.1:p.Ala357=
NM_001286044.2:c.405T>G	NP_001272973.1:p.Ala135=