Canonical Allele Identifier: CA340817932
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761165T>C , CM000663.2:g.75761165T>C GRCh38
NC_000001.10:g.76226850T>C , CM000663.1:g.76226850T>C GRCh37
NC_000001.9:g.75999438T>C NCBI36
NG_007045.2:g.41808T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.989T>C MANE Select ENSP00000359878.5:p.Val330Ala
ENST00000473018.3:n.3113T>C
ENST00000532207.6:n.2000T>C
ENST00000541113.6:c.893T>C ENSP00000442324.2:p.Val298Ala
ENST00000679509.1:n.1951T>C
ENST00000679530.1:c.*757T>C ENSP00000506454.1:n.*757T>C
ENST00000679615.1:n.3004T>C
ENST00000679687.1:c.551T>C ENSP00000506598.1:p.Val184Ala
ENST00000679704.1:c.*755T>C ENSP00000505117.1:n.*755T>C
ENST00000679709.1:c.*952T>C ENSP00000506623.1:n.*952T>C
ENST00000679976.1:c.*573T>C ENSP00000505565.1:n.*573T>C
ENST00000680166.1:n.4278T>C
ENST00000680315.1:n.872T>C
ENST00000680517.1:c.*377T>C ENSP00000505803.1:n.*377T>C
ENST00000680582.1:n.1951T>C
ENST00000680613.1:c.*482T>C ENSP00000506114.1:n.*482T>C
ENST00000680662.1:c.*903T>C ENSP00000505080.1:n.*903T>C
ENST00000680691.1:c.*652T>C ENSP00000506487.1:n.*652T>C
ENST00000680694.1:c.*577T>C ENSP00000505658.1:n.*577T>C
ENST00000680743.1:c.*778T>C ENSP00000505073.1:n.*778T>C
ENST00000680749.1:c.*274T>C ENSP00000505122.1:n.*274T>C
ENST00000680798.1:c.*464T>C ENSP00000505670.1:n.*464T>C
ENST00000680805.1:c.848T>C ENSP00000505447.1:p.Val283Ala
ENST00000680844.1:c.*773T>C ENSP00000506541.1:n.*773T>C
ENST00000680948.1:c.*856T>C ENSP00000505441.1:n.*856T>C
ENST00000680964.1:c.*82T>C ENSP00000505961.1:n.*82T>C
ENST00000681037.1:c.*2473T>C ENSP00000506025.1:n.*2473T>C
ENST00000681063.1:c.*258T>C ENSP00000506616.1:n.*258T>C
ENST00000681209.1:c.*644T>C ENSP00000505877.1:n.*644T>C
ENST00000681278.1:n.1691T>C
ENST00000681289.1:n.4984T>C
ENST00000681361.1:c.*656T>C ENSP00000506679.1:n.*656T>C
ENST00000681430.1:c.*82T>C ENSP00000506301.1:n.*82T>C
ENST00000681446.1:c.*693T>C ENSP00000506244.1:n.*693T>C
ENST00000681450.1:c.*660T>C ENSP00000505660.1:n.*660T>C
ENST00000681548.1:c.*575T>C ENSP00000505275.1:n.*575T>C
ENST00000681616.1:c.*648T>C ENSP00000505111.1:n.*648T>C
ENST00000681621.1:c.*573T>C ENSP00000505770.1:n.*573T>C
ENST00000681680.1:n.3084T>C
ENST00000681720.1:c.*444T>C ENSP00000505438.1:n.*444T>C
ENST00000681730.1:n.1211T>C
ENST00000681790.1:c.731T>C ENSP00000505130.1:p.Val244Ala
ENST00000681837.1:n.1605T>C
ENST00000681913.1:n.3235T>C
ENST00000681916.1:c.*757T>C ENSP00000506477.1:n.*757T>C
ENST00000681930.1:n.3113T>C
ENST00000370834.9:c.1088T>C ENSP00000359871.5:p.Val363Ala
ENST00000370841.8:c.989T>C ENSP00000359878.4:p.Val330Ala
ENST00000420607.6:c.1001T>C ENSP00000409612.2:p.Val334Ala
ENST00000481374.1:n.262T>C
ENST00000525808.5:c.*575T>C ENSP00000434823.1:n.*575T>C
ENST00000526129.5:c.*773T>C ENSP00000434092.1:n.*773T>C
ENST00000526196.5:c.*757T>C ENSP00000431953.1:n.*757T>C
ENST00000528016.1:c.160-8012T>C ENSP00000434284.1:n.160-8012T>C
ENST00000529059.5:n.898T>C
ENST00000532207.5:n.719T>C
ENST00000534334.5:c.*730T>C ENSP00000435584.1:n.*730T>C
ENST00000541113.5:c.881T>C ENSP00000442324.1:p.Val294Ala
NM_000016.5:c.989T>C NP_000007.1:p.Val330Ala
NM_001127328.2:c.1001T>C NP_001120800.1:p.Val334Ala
NM_001286042.1:c.881T>C NP_001272971.1:p.Val294Ala
NM_001286043.1:c.1088T>C NP_001272972.1:p.Val363Ala
NM_001286044.1:c.422T>C NP_001272973.1:p.Val141Ala
NM_000016.6:c.989T>C MANE Select NP_000007.1:p.Val330Ala
NM_001127328.3:c.1001T>C NP_001120800.1:p.Val334Ala
NM_001286042.2:c.881T>C NP_001272971.1:p.Val294Ala
NM_001286043.2:c.1088T>C NP_001272972.1:p.Val363Ala
NM_001286044.2:c.422T>C NP_001272973.1:p.Val141Ala