Canonical Allele Identifier: CA1140596686

Gene: ACADM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75739996_75739997delinsAA , CM000663.2:g.75739996_75739997delinsAA	GRCh38
NC_000001.10:g.76205681_76205682delinsAA , CM000663.1:g.76205681_76205682delinsAA	GRCh37
NC_000001.9:g.75978269_75978270delinsAA	NCBI36
NG_007045.2:g.20639_20640delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.485_486delinsAA MANE Select	ENSP00000359878.5:p.Glu162=
ENST00000473018.3:n.2609_2610delinsAA
ENST00000541113.6:c.485_486delinsAA	ENSP00000442324.2:p.Glu162=
ENST00000679509.1:n.1447_1448delinsAA
ENST00000679530.1:c.*253_*254delinsAA	ENSP00000506454.1:n.*253_*254delinsAA
ENST00000679615.1:n.2609_2610delinsAA
ENST00000679687.1:c.47_48delinsAA	ENSP00000506598.1:p.Glu16=
ENST00000679704.1:c.*251_*252delinsAA	ENSP00000505117.1:n.*251_*252delinsAA
ENST00000679709.1:c.*448_*449delinsAA	ENSP00000506623.1:n.*448_*449delinsAA
ENST00000679804.1:n.224_225delinsAA
ENST00000679976.1:c.*69_*70delinsAA	ENSP00000505565.1:n.*69_*70delinsAA
ENST00000680166.1:n.3774_3775delinsAA
ENST00000680517.1:c.303_304delinsAA	ENSP00000505803.1:p.Arg101=
ENST00000680582.1:n.1447_1448delinsAA
ENST00000680613.1:c.485_486delinsAA	ENSP00000506114.1:p.Glu162=
ENST00000680662.1:c.*399_*400delinsAA	ENSP00000505080.1:n.*399_*400delinsAA
ENST00000680691.1:c.*148_*149delinsAA	ENSP00000506487.1:n.*148_*149delinsAA
ENST00000680694.1:c.*73_*74delinsAA	ENSP00000505658.1:n.*73_*74delinsAA
ENST00000680743.1:c.*152_*153delinsAA	ENSP00000505073.1:n.*152_*153delinsAA
ENST00000680749.1:c.485_486delinsAA	ENSP00000505122.1:p.Glu162=
ENST00000680798.1:c.*69_*70delinsAA	ENSP00000505670.1:n.*69_*70delinsAA
ENST00000680805.1:c.485_486delinsAA	ENSP00000505447.1:p.Glu162=
ENST00000680844.1:c.*269_*270delinsAA	ENSP00000506541.1:n.*269_*270delinsAA
ENST00000680948.1:c.*352_*353delinsAA	ENSP00000505441.1:n.*352_*353delinsAA
ENST00000680964.1:c.485_486delinsAA	ENSP00000505961.1:p.Glu162=
ENST00000681037.1:c.485_486delinsAA	ENSP00000506025.1:p.Glu162=
ENST00000681063.1:c.485_486delinsAA	ENSP00000506616.1:p.Glu162=
ENST00000681209.1:c.*249_*250delinsAA	ENSP00000505877.1:n.*249_*250delinsAA
ENST00000681278.1:n.842_843delinsAA
ENST00000681289.1:n.842_843delinsAA
ENST00000681361.1:c.*152_*153delinsAA	ENSP00000506679.1:n.*152_*153delinsAA
ENST00000681430.1:c.485_486delinsAA	ENSP00000506301.1:p.Glu162=
ENST00000681446.1:c.*67_*68delinsAA	ENSP00000506244.1:n.*67_*68delinsAA
ENST00000681450.1:c.*156_*157delinsAA	ENSP00000505660.1:n.*156_*157delinsAA
ENST00000681548.1:c.*71_*72delinsAA	ENSP00000505275.1:n.*71_*72delinsAA
ENST00000681616.1:c.*253_*254delinsAA	ENSP00000505111.1:n.*253_*254delinsAA
ENST00000681621.1:c.*69_*70delinsAA	ENSP00000505770.1:n.*69_*70delinsAA
ENST00000681680.1:n.2609_2610delinsAA
ENST00000681720.1:c.*55-5810_*55-5809delinsAA	ENSP00000505438.1:n.*55-5810_*55-5809delinsAA
ENST00000681730.1:n.707_708delinsAA
ENST00000681790.1:c.227_228delinsAA	ENSP00000505130.1:p.Glu76=
ENST00000681837.1:n.1101_1102delinsAA
ENST00000681913.1:n.2609_2610delinsAA
ENST00000681916.1:c.*253_*254delinsAA	ENSP00000506477.1:n.*253_*254delinsAA
ENST00000681930.1:n.2609_2610delinsAA
ENST00000370834.9:c.584_585delinsAA	ENSP00000359871.5:p.Glu195=
ENST00000370841.8:c.485_486delinsAA	ENSP00000359878.4:p.Glu162=
ENST00000420607.6:c.497_498delinsAA	ENSP00000409612.2:p.Glu166=
ENST00000525808.5:c.*71_*72delinsAA	ENSP00000434823.1:n.*71_*72delinsAA
ENST00000526129.5:c.*269_*270delinsAA	ENSP00000434092.1:n.*269_*270delinsAA
ENST00000526196.5:c.*253_*254delinsAA	ENSP00000431953.1:n.*253_*254delinsAA
ENST00000526930.1:n.258_259delinsAA
ENST00000529059.5:n.394_395delinsAA
ENST00000530953.6:c.135_136delinsAA	ENSP00000431372.1:p.Arg45=
ENST00000532509.5:c.*249_*250delinsAA	ENSP00000432522.1:n.*249_*250delinsAA
ENST00000534334.5:c.*69_*70delinsAA	ENSP00000435584.1:n.*69_*70delinsAA
ENST00000541113.5:c.377_378delinsAA	ENSP00000442324.1:p.Glu126=
NM_000016.5:c.485_486delinsAA	NP_000007.1:p.Glu162=
NM_001127328.2:c.497_498delinsAA	NP_001120800.1:p.Glu166=
NM_001286042.1:c.377_378delinsAA	NP_001272971.1:p.Glu126=
NM_001286043.1:c.584_585delinsAA	NP_001272972.1:p.Glu195=
NM_001286044.1:c.-83_-82delinsAA	NP_001272973.1:n.-83_-82delinsAA
NM_000016.6:c.485_486delinsAA MANE Select	NP_000007.1:p.Glu162=
NM_001127328.3:c.497_498delinsAA	NP_001120800.1:p.Glu166=
NM_001286042.2:c.377_378delinsAA	NP_001272971.1:p.Glu126=
NM_001286043.2:c.584_585delinsAA	NP_001272972.1:p.Glu195=
NM_001286044.2:c.-83_-82delinsAA	NP_001272973.1:n.-83_-82delinsAA