Canonical Allele Identifier: CA340816668
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75749495T>C , CM000663.2:g.75749495T>C GRCh38
NC_000001.10:g.76215180T>C , CM000663.1:g.76215180T>C GRCh37
NC_000001.9:g.75987768T>C NCBI36
NG_007045.2:g.30138T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.785T>C MANE Select ENSP00000359878.5:p.Val262Ala
ENST00000473018.3:n.2909T>C
ENST00000532207.6:n.1674T>C
ENST00000541113.6:c.785T>C ENSP00000442324.2:p.Val262Ala
ENST00000679509.1:n.1747T>C
ENST00000679530.1:c.*553T>C ENSP00000506454.1:n.*553T>C
ENST00000679615.1:n.2800T>C
ENST00000679687.1:c.347T>C ENSP00000506598.1:p.Val116Ala
ENST00000679704.1:c.*551T>C ENSP00000505117.1:n.*551T>C
ENST00000679709.1:c.*748T>C ENSP00000506623.1:n.*748T>C
ENST00000679976.1:c.*369T>C ENSP00000505565.1:n.*369T>C
ENST00000680166.1:n.4074T>C
ENST00000680517.1:c.*173T>C ENSP00000505803.1:n.*173T>C
ENST00000680582.1:n.1747T>C
ENST00000680613.1:c.*156T>C ENSP00000506114.1:n.*156T>C
ENST00000680662.1:c.*699T>C ENSP00000505080.1:n.*699T>C
ENST00000680691.1:c.*448T>C ENSP00000506487.1:n.*448T>C
ENST00000680694.1:c.*373T>C ENSP00000505658.1:n.*373T>C
ENST00000680743.1:c.*452T>C ENSP00000505073.1:n.*452T>C
ENST00000680749.1:c.*70T>C ENSP00000505122.1:n.*70T>C
ENST00000680798.1:c.*260T>C ENSP00000505670.1:n.*260T>C
ENST00000680805.1:c.709-956T>C ENSP00000505447.1:n.709-956T>C
ENST00000680844.1:c.*569T>C ENSP00000506541.1:n.*569T>C
ENST00000680948.1:c.*652T>C ENSP00000505441.1:n.*652T>C
ENST00000680964.1:c.785T>C ENSP00000505961.1:p.Val262Ala
ENST00000681037.1:c.*2269T>C ENSP00000506025.1:n.*2269T>C
ENST00000681063.1:c.600-956T>C ENSP00000506616.1:n.600-956T>C
ENST00000681209.1:c.*440T>C ENSP00000505877.1:n.*440T>C
ENST00000681278.1:n.1142T>C
ENST00000681289.1:n.4780T>C
ENST00000681361.1:c.*452T>C ENSP00000506679.1:n.*452T>C
ENST00000681430.1:c.785T>C ENSP00000506301.1:p.Val262Ala
ENST00000681446.1:c.*367T>C ENSP00000506244.1:n.*367T>C
ENST00000681450.1:c.*456T>C ENSP00000505660.1:n.*456T>C
ENST00000681548.1:c.*371T>C ENSP00000505275.1:n.*371T>C
ENST00000681616.1:c.*444T>C ENSP00000505111.1:n.*444T>C
ENST00000681621.1:c.*369T>C ENSP00000505770.1:n.*369T>C
ENST00000681680.1:n.2880T>C
ENST00000681720.1:c.*240T>C ENSP00000505438.1:n.*240T>C
ENST00000681730.1:n.1007T>C
ENST00000681790.1:c.527T>C ENSP00000505130.1:p.Val176Ala
ENST00000681837.1:n.1401T>C
ENST00000681913.1:n.2909T>C
ENST00000681916.1:c.*553T>C ENSP00000506477.1:n.*553T>C
ENST00000681930.1:n.2909T>C
ENST00000370834.9:c.884T>C ENSP00000359871.5:p.Val295Ala
ENST00000370841.8:c.785T>C ENSP00000359878.4:p.Val262Ala
ENST00000420607.6:c.797T>C ENSP00000409612.2:p.Val266Ala
ENST00000525808.5:c.*371T>C ENSP00000434823.1:n.*371T>C
ENST00000526129.5:c.*569T>C ENSP00000434092.1:n.*569T>C
ENST00000526196.5:c.*553T>C ENSP00000431953.1:n.*553T>C
ENST00000526930.1:n.558T>C
ENST00000529059.5:n.694T>C
ENST00000530953.6:c.*282T>C ENSP00000431372.1:n.*282T>C
ENST00000532207.5:n.515T>C
ENST00000532509.5:c.*549T>C ENSP00000432522.1:n.*549T>C
ENST00000534334.5:c.*369T>C ENSP00000435584.1:n.*369T>C
ENST00000541113.5:c.677T>C ENSP00000442324.1:p.Val226Ala
NM_000016.5:c.785T>C NP_000007.1:p.Val262Ala
NM_001127328.2:c.797T>C NP_001120800.1:p.Val266Ala
NM_001286042.1:c.677T>C NP_001272971.1:p.Val226Ala
NM_001286043.1:c.884T>C NP_001272972.1:p.Val295Ala
NM_001286044.1:c.218T>C NP_001272973.1:p.Val73Ala
NM_000016.6:c.785T>C MANE Select NP_000007.1:p.Val262Ala
NM_001127328.3:c.797T>C NP_001120800.1:p.Val266Ala
NM_001286042.2:c.677T>C NP_001272971.1:p.Val226Ala
NM_001286043.2:c.884T>C NP_001272972.1:p.Val295Ala
NM_001286044.2:c.218T>C NP_001272973.1:p.Val73Ala