Canonical Allele Identifier: CA418539908
Gene: ACADM HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.76205703A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75740018A>C , CM000663.2:g.75740018A>C GRCh38
NC_000001.10:g.76205703A>C , CM000663.1:g.76205703A>C GRCh37
NC_000001.9:g.75978291A>C NCBI36
NG_007045.2:g.20661A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.507A>C MANE Select ENSP00000359878.5:p.Val169=
ENST00000473018.3:n.2631A>C
ENST00000541113.6:c.507A>C ENSP00000442324.2:p.Val169=
ENST00000679509.1:n.1469A>C
ENST00000679530.1:c.*275A>C ENSP00000506454.1:n.*275A>C
ENST00000679615.1:n.2631A>C
ENST00000679687.1:c.69A>C ENSP00000506598.1:p.Val23=
ENST00000679704.1:c.*273A>C ENSP00000505117.1:n.*273A>C
ENST00000679709.1:c.*470A>C ENSP00000506623.1:n.*470A>C
ENST00000679804.1:n.246A>C
ENST00000679976.1:c.*91A>C ENSP00000505565.1:n.*91A>C
ENST00000680166.1:n.3796A>C
ENST00000680517.1:c.*4A>C ENSP00000505803.1:n.*4A>C
ENST00000680582.1:n.1469A>C
ENST00000680613.1:c.507A>C ENSP00000506114.1:p.Val169=
ENST00000680662.1:c.*421A>C ENSP00000505080.1:n.*421A>C
ENST00000680691.1:c.*170A>C ENSP00000506487.1:n.*170A>C
ENST00000680694.1:c.*95A>C ENSP00000505658.1:n.*95A>C
ENST00000680743.1:c.*174A>C ENSP00000505073.1:n.*174A>C
ENST00000680749.1:c.507A>C ENSP00000505122.1:p.Val169=
ENST00000680798.1:c.*91A>C ENSP00000505670.1:n.*91A>C
ENST00000680805.1:c.507A>C ENSP00000505447.1:p.Val169=
ENST00000680844.1:c.*291A>C ENSP00000506541.1:n.*291A>C
ENST00000680948.1:c.*374A>C ENSP00000505441.1:n.*374A>C
ENST00000680964.1:c.507A>C ENSP00000505961.1:p.Val169=
ENST00000681037.1:c.507A>C ENSP00000506025.1:p.Val169=
ENST00000681063.1:c.507A>C ENSP00000506616.1:p.Val169=
ENST00000681209.1:c.*271A>C ENSP00000505877.1:n.*271A>C
ENST00000681278.1:n.864A>C
ENST00000681289.1:n.864A>C
ENST00000681361.1:c.*174A>C ENSP00000506679.1:n.*174A>C
ENST00000681430.1:c.507A>C ENSP00000506301.1:p.Val169=
ENST00000681446.1:c.*89A>C ENSP00000506244.1:n.*89A>C
ENST00000681450.1:c.*178A>C ENSP00000505660.1:n.*178A>C
ENST00000681548.1:c.*93A>C ENSP00000505275.1:n.*93A>C
ENST00000681616.1:c.*275A>C ENSP00000505111.1:n.*275A>C
ENST00000681621.1:c.*91A>C ENSP00000505770.1:n.*91A>C
ENST00000681680.1:n.2631A>C
ENST00000681720.1:c.*55-5788A>C ENSP00000505438.1:n.*55-5788A>C
ENST00000681730.1:n.729A>C
ENST00000681790.1:c.249A>C ENSP00000505130.1:p.Val83=
ENST00000681837.1:n.1123A>C
ENST00000681913.1:n.2631A>C
ENST00000681916.1:c.*275A>C ENSP00000506477.1:n.*275A>C
ENST00000681930.1:n.2631A>C
ENST00000370834.9:c.606A>C ENSP00000359871.5:p.Val202=
ENST00000370841.8:c.507A>C ENSP00000359878.4:p.Val169=
ENST00000420607.6:c.519A>C ENSP00000409612.2:p.Val173=
ENST00000525808.5:c.*93A>C ENSP00000434823.1:n.*93A>C
ENST00000526129.5:c.*291A>C ENSP00000434092.1:n.*291A>C
ENST00000526196.5:c.*275A>C ENSP00000431953.1:n.*275A>C
ENST00000526930.1:n.280A>C
ENST00000529059.5:n.416A>C
ENST00000530953.6:c.*4A>C ENSP00000431372.1:n.*4A>C
ENST00000532509.5:c.*271A>C ENSP00000432522.1:n.*271A>C
ENST00000534334.5:c.*91A>C ENSP00000435584.1:n.*91A>C
ENST00000541113.5:c.399A>C ENSP00000442324.1:p.Val133=
NM_000016.5:c.507A>C NP_000007.1:p.Val169=
NM_001127328.2:c.519A>C NP_001120800.1:p.Val173=
NM_001286042.1:c.399A>C NP_001272971.1:p.Val133=
NM_001286043.1:c.606A>C NP_001272972.1:p.Val202=
NM_001286044.1:c.-61A>C NP_001272973.1:n.-61A>C
NM_000016.6:c.507A>C MANE Select NP_000007.1:p.Val169=
NM_001127328.3:c.519A>C NP_001120800.1:p.Val173=
NM_001286042.2:c.399A>C NP_001272971.1:p.Val133=
NM_001286043.2:c.606A>C NP_001272972.1:p.Val202=
NM_001286044.2:c.-61A>C NP_001272973.1:n.-61A>C