Canonical Allele Identifier: CA340816622
Gene: ACADM HGNC NCBI

Linked Data

gnomAD v4: 1-75749474-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75749474T>A , CM000663.2:g.75749474T>A GRCh38
NC_000001.10:g.76215159T>A , CM000663.1:g.76215159T>A GRCh37
NC_000001.9:g.75987747T>A NCBI36
NG_007045.2:g.30117T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.764T>A MANE Select ENSP00000359878.5:p.Val255Glu
ENST00000473018.3:n.2888T>A
ENST00000532207.6:n.1653T>A
ENST00000541113.6:c.764T>A ENSP00000442324.2:p.Val255Glu
ENST00000679509.1:n.1726T>A
ENST00000679530.1:c.*532T>A ENSP00000506454.1:n.*532T>A
ENST00000679615.1:n.2779T>A
ENST00000679687.1:c.326T>A ENSP00000506598.1:p.Val109Glu
ENST00000679704.1:c.*530T>A ENSP00000505117.1:n.*530T>A
ENST00000679709.1:c.*727T>A ENSP00000506623.1:n.*727T>A
ENST00000679976.1:c.*348T>A ENSP00000505565.1:n.*348T>A
ENST00000680166.1:n.4053T>A
ENST00000680517.1:c.*152T>A ENSP00000505803.1:n.*152T>A
ENST00000680582.1:n.1726T>A
ENST00000680613.1:c.*135T>A ENSP00000506114.1:n.*135T>A
ENST00000680662.1:c.*678T>A ENSP00000505080.1:n.*678T>A
ENST00000680691.1:c.*427T>A ENSP00000506487.1:n.*427T>A
ENST00000680694.1:c.*352T>A ENSP00000505658.1:n.*352T>A
ENST00000680743.1:c.*431T>A ENSP00000505073.1:n.*431T>A
ENST00000680749.1:c.*49T>A ENSP00000505122.1:n.*49T>A
ENST00000680798.1:c.*239T>A ENSP00000505670.1:n.*239T>A
ENST00000680805.1:c.709-977T>A ENSP00000505447.1:n.709-977T>A
ENST00000680844.1:c.*548T>A ENSP00000506541.1:n.*548T>A
ENST00000680948.1:c.*631T>A ENSP00000505441.1:n.*631T>A
ENST00000680964.1:c.764T>A ENSP00000505961.1:p.Val255Glu
ENST00000681037.1:c.*2248T>A ENSP00000506025.1:n.*2248T>A
ENST00000681063.1:c.600-977T>A ENSP00000506616.1:n.600-977T>A
ENST00000681209.1:c.*419T>A ENSP00000505877.1:n.*419T>A
ENST00000681278.1:n.1121T>A
ENST00000681289.1:n.4759T>A
ENST00000681361.1:c.*431T>A ENSP00000506679.1:n.*431T>A
ENST00000681430.1:c.764T>A ENSP00000506301.1:p.Val255Glu
ENST00000681446.1:c.*346T>A ENSP00000506244.1:n.*346T>A
ENST00000681450.1:c.*435T>A ENSP00000505660.1:n.*435T>A
ENST00000681548.1:c.*350T>A ENSP00000505275.1:n.*350T>A
ENST00000681616.1:c.*423T>A ENSP00000505111.1:n.*423T>A
ENST00000681621.1:c.*348T>A ENSP00000505770.1:n.*348T>A
ENST00000681680.1:n.2859T>A
ENST00000681720.1:c.*219T>A ENSP00000505438.1:n.*219T>A
ENST00000681730.1:n.986T>A
ENST00000681790.1:c.506T>A ENSP00000505130.1:p.Val169Glu
ENST00000681837.1:n.1380T>A
ENST00000681913.1:n.2888T>A
ENST00000681916.1:c.*532T>A ENSP00000506477.1:n.*532T>A
ENST00000681930.1:n.2888T>A
ENST00000370834.9:c.863T>A ENSP00000359871.5:p.Val288Glu
ENST00000370841.8:c.764T>A ENSP00000359878.4:p.Val255Glu
ENST00000420607.6:c.776T>A ENSP00000409612.2:p.Val259Glu
ENST00000525808.5:c.*350T>A ENSP00000434823.1:n.*350T>A
ENST00000526129.5:c.*548T>A ENSP00000434092.1:n.*548T>A
ENST00000526196.5:c.*532T>A ENSP00000431953.1:n.*532T>A
ENST00000526930.1:n.537T>A
ENST00000529059.5:n.673T>A
ENST00000530953.6:c.*261T>A ENSP00000431372.1:n.*261T>A
ENST00000532207.5:n.494T>A
ENST00000532509.5:c.*528T>A ENSP00000432522.1:n.*528T>A
ENST00000534334.5:c.*348T>A ENSP00000435584.1:n.*348T>A
ENST00000541113.5:c.656T>A ENSP00000442324.1:p.Val219Glu
NM_000016.5:c.764T>A NP_000007.1:p.Val255Glu
NM_001127328.2:c.776T>A NP_001120800.1:p.Val259Glu
NM_001286042.1:c.656T>A NP_001272971.1:p.Val219Glu
NM_001286043.1:c.863T>A NP_001272972.1:p.Val288Glu
NM_001286044.1:c.197T>A NP_001272973.1:p.Val66Glu
NM_000016.6:c.764T>A MANE Select NP_000007.1:p.Val255Glu
NM_001127328.3:c.776T>A NP_001120800.1:p.Val259Glu
NM_001286042.2:c.656T>A NP_001272971.1:p.Val219Glu
NM_001286043.2:c.863T>A NP_001272972.1:p.Val288Glu
NM_001286044.2:c.197T>A NP_001272973.1:p.Val66Glu