Canonical Allele Identifier: CA1176726824
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761187C= , CM000663.2:g.75761187C= GRCh38
NC_000001.10:g.76226872C= , CM000663.1:g.76226872C= GRCh37
NC_000001.9:g.75999460C= NCBI36
NG_007045.2:g.41830C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.1011C= MANE Select ENSP00000359878.5:p.Tyr337=
ENST00000473018.3:n.3135C=
ENST00000532207.6:n.2022C=
ENST00000541113.6:c.915C= ENSP00000442324.2:p.Tyr305=
ENST00000679509.1:n.1973C=
ENST00000679530.1:c.*779C= ENSP00000506454.1:n.*779C=
ENST00000679615.1:n.3026C=
ENST00000679687.1:c.573C= ENSP00000506598.1:p.Tyr191=
ENST00000679704.1:c.*777C= ENSP00000505117.1:n.*777C=
ENST00000679709.1:c.*974C= ENSP00000506623.1:n.*974C=
ENST00000679976.1:c.*595C= ENSP00000505565.1:n.*595C=
ENST00000680166.1:n.4300C=
ENST00000680315.1:n.894C=
ENST00000680517.1:c.*399C= ENSP00000505803.1:n.*399C=
ENST00000680582.1:n.1973C=
ENST00000680613.1:c.*504C= ENSP00000506114.1:n.*504C=
ENST00000680662.1:c.*925C= ENSP00000505080.1:n.*925C=
ENST00000680691.1:c.*674C= ENSP00000506487.1:n.*674C=
ENST00000680694.1:c.*599C= ENSP00000505658.1:n.*599C=
ENST00000680743.1:c.*800C= ENSP00000505073.1:n.*800C=
ENST00000680749.1:c.*296C= ENSP00000505122.1:n.*296C=
ENST00000680798.1:c.*486C= ENSP00000505670.1:n.*486C=
ENST00000680805.1:c.870C= ENSP00000505447.1:p.Tyr290=
ENST00000680844.1:c.*795C= ENSP00000506541.1:n.*795C=
ENST00000680948.1:c.*878C= ENSP00000505441.1:n.*878C=
ENST00000680964.1:c.*104C= ENSP00000505961.1:n.*104C=
ENST00000681037.1:c.*2495C= ENSP00000506025.1:n.*2495C=
ENST00000681063.1:c.*280C= ENSP00000506616.1:n.*280C=
ENST00000681209.1:c.*666C= ENSP00000505877.1:n.*666C=
ENST00000681278.1:n.1713C=
ENST00000681289.1:n.5006C=
ENST00000681361.1:c.*678C= ENSP00000506679.1:n.*678C=
ENST00000681430.1:c.*104C= ENSP00000506301.1:n.*104C=
ENST00000681446.1:c.*715C= ENSP00000506244.1:n.*715C=
ENST00000681450.1:c.*682C= ENSP00000505660.1:n.*682C=
ENST00000681548.1:c.*597C= ENSP00000505275.1:n.*597C=
ENST00000681616.1:c.*670C= ENSP00000505111.1:n.*670C=
ENST00000681621.1:c.*595C= ENSP00000505770.1:n.*595C=
ENST00000681680.1:n.3106C=
ENST00000681720.1:c.*466C= ENSP00000505438.1:n.*466C=
ENST00000681730.1:n.1233C=
ENST00000681790.1:c.753C= ENSP00000505130.1:p.Tyr251=
ENST00000681837.1:n.1627C=
ENST00000681913.1:n.3257C=
ENST00000681916.1:c.*779C= ENSP00000506477.1:n.*779C=
ENST00000681930.1:n.3135C=
ENST00000370834.9:c.1110C= ENSP00000359871.5:p.Tyr370=
ENST00000370841.8:c.1011C= ENSP00000359878.4:p.Tyr337=
ENST00000420607.6:c.1023C= ENSP00000409612.2:p.Tyr341=
ENST00000481374.1:n.284C=
ENST00000525808.5:c.*597C= ENSP00000434823.1:n.*597C=
ENST00000526129.5:c.*795C= ENSP00000434092.1:n.*795C=
ENST00000526196.5:c.*779C= ENSP00000431953.1:n.*779C=
ENST00000528016.1:c.160-7990C= ENSP00000434284.1:n.160-7990C=
ENST00000529059.5:n.920C=
ENST00000532207.5:n.741C=
ENST00000534334.5:c.*752C= ENSP00000435584.1:n.*752C=
ENST00000541113.5:c.903C= ENSP00000442324.1:p.Tyr301=
NM_000016.5:c.1011C= NP_000007.1:p.Tyr337=
NM_001127328.2:c.1023C= NP_001120800.1:p.Tyr341=
NM_001286042.1:c.903C= NP_001272971.1:p.Tyr301=
NM_001286043.1:c.1110C= NP_001272972.1:p.Tyr370=
NM_001286044.1:c.444C= NP_001272973.1:p.Tyr148=
NM_000016.6:c.1011C= MANE Select NP_000007.1:p.Tyr337=
NM_001127328.3:c.1023C= NP_001120800.1:p.Tyr341=
NM_001286042.2:c.903C= NP_001272971.1:p.Tyr301=
NM_001286043.2:c.1110C= NP_001272972.1:p.Tyr370=
NM_001286044.2:c.444C= NP_001272973.1:p.Tyr148=