Canonical Allele Identifier: CA418544958

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76215235C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75749550C>G , CM000663.2:g.75749550C>G	GRCh38
NC_000001.10:g.76215235C>G , CM000663.1:g.76215235C>G	GRCh37
NC_000001.9:g.75987823C>G	NCBI36
NG_007045.2:g.30193C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.840C>G MANE Select	ENSP00000359878.5:p.Thr280=
ENST00000473018.3:n.2964C>G
ENST00000532207.6:n.1729C>G
ENST00000541113.6:c.840C>G	ENSP00000442324.2:p.Thr280=
ENST00000679509.1:n.1802C>G
ENST00000679530.1:c.*608C>G	ENSP00000506454.1:n.*608C>G
ENST00000679615.1:n.2855C>G
ENST00000679687.1:c.402C>G	ENSP00000506598.1:p.Thr134=
ENST00000679704.1:c.*606C>G	ENSP00000505117.1:n.*606C>G
ENST00000679709.1:c.*803C>G	ENSP00000506623.1:n.*803C>G
ENST00000679976.1:c.*424C>G	ENSP00000505565.1:n.*424C>G
ENST00000680166.1:n.4129C>G
ENST00000680517.1:c.*228C>G	ENSP00000505803.1:n.*228C>G
ENST00000680582.1:n.1802C>G
ENST00000680613.1:c.*211C>G	ENSP00000506114.1:n.*211C>G
ENST00000680662.1:c.*754C>G	ENSP00000505080.1:n.*754C>G
ENST00000680691.1:c.*503C>G	ENSP00000506487.1:n.*503C>G
ENST00000680694.1:c.*428C>G	ENSP00000505658.1:n.*428C>G
ENST00000680743.1:c.*507C>G	ENSP00000505073.1:n.*507C>G
ENST00000680749.1:c.*125C>G	ENSP00000505122.1:n.*125C>G
ENST00000680798.1:c.*315C>G	ENSP00000505670.1:n.*315C>G
ENST00000680805.1:c.709-901C>G	ENSP00000505447.1:n.709-901C>G
ENST00000680844.1:c.*624C>G	ENSP00000506541.1:n.*624C>G
ENST00000680948.1:c.*707C>G	ENSP00000505441.1:n.*707C>G
ENST00000680964.1:c.840C>G	ENSP00000505961.1:p.Thr280=
ENST00000681037.1:c.*2324C>G	ENSP00000506025.1:n.*2324C>G
ENST00000681063.1:c.600-901C>G	ENSP00000506616.1:n.600-901C>G
ENST00000681209.1:c.*495C>G	ENSP00000505877.1:n.*495C>G
ENST00000681278.1:n.1197C>G
ENST00000681289.1:n.4835C>G
ENST00000681361.1:c.*507C>G	ENSP00000506679.1:n.*507C>G
ENST00000681430.1:c.840C>G	ENSP00000506301.1:p.Thr280=
ENST00000681446.1:c.*422C>G	ENSP00000506244.1:n.*422C>G
ENST00000681450.1:c.*511C>G	ENSP00000505660.1:n.*511C>G
ENST00000681548.1:c.*426C>G	ENSP00000505275.1:n.*426C>G
ENST00000681616.1:c.*499C>G	ENSP00000505111.1:n.*499C>G
ENST00000681621.1:c.*424C>G	ENSP00000505770.1:n.*424C>G
ENST00000681680.1:n.2935C>G
ENST00000681720.1:c.*295C>G	ENSP00000505438.1:n.*295C>G
ENST00000681730.1:n.1062C>G
ENST00000681790.1:c.582C>G	ENSP00000505130.1:p.Thr194=
ENST00000681837.1:n.1456C>G
ENST00000681913.1:n.2964C>G
ENST00000681916.1:c.*608C>G	ENSP00000506477.1:n.*608C>G
ENST00000681930.1:n.2964C>G
ENST00000370834.9:c.939C>G	ENSP00000359871.5:p.Thr313=
ENST00000370841.8:c.840C>G	ENSP00000359878.4:p.Thr280=
ENST00000420607.6:c.852C>G	ENSP00000409612.2:p.Thr284=
ENST00000525808.5:c.*426C>G	ENSP00000434823.1:n.*426C>G
ENST00000526129.5:c.*624C>G	ENSP00000434092.1:n.*624C>G
ENST00000526196.5:c.*608C>G	ENSP00000431953.1:n.*608C>G
ENST00000528016.1:c.54C>G	ENSP00000434284.1:p.Thr18=
ENST00000529059.5:n.749C>G
ENST00000532207.5:n.570C>G
ENST00000532509.5:c.*604C>G	ENSP00000432522.1:n.*604C>G
ENST00000534334.5:c.*424C>G	ENSP00000435584.1:n.*424C>G
ENST00000541113.5:c.732C>G	ENSP00000442324.1:p.Thr244=
NM_000016.5:c.840C>G	NP_000007.1:p.Thr280=
NM_001127328.2:c.852C>G	NP_001120800.1:p.Thr284=
NM_001286042.1:c.732C>G	NP_001272971.1:p.Thr244=
NM_001286043.1:c.939C>G	NP_001272972.1:p.Thr313=
NM_001286044.1:c.273C>G	NP_001272973.1:p.Thr91=
NM_000016.6:c.840C>G MANE Select	NP_000007.1:p.Thr280=
NM_001127328.3:c.852C>G	NP_001120800.1:p.Thr284=
NM_001286042.2:c.732C>G	NP_001272971.1:p.Thr244=
NM_001286043.2:c.939C>G	NP_001272972.1:p.Thr313=
NM_001286044.2:c.273C>G	NP_001272973.1:p.Thr91=