Canonical Allele Identifier: CA1176715729

Gene: ACADM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75740049_75740051delinsGGA , CM000663.2:g.75740049_75740051delinsGGA	GRCh38
NC_000001.10:g.76205734_76205736delinsGGA , CM000663.1:g.76205734_76205736delinsGGA	GRCh37
NC_000001.9:g.75978322_75978324delinsGGA	NCBI36
NG_007045.2:g.20692_20694delinsGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.538_540delinsGGA MANE Select	ENSP00000359878.5:p.Gly180=
ENST00000473018.3:n.2662_2664delinsGGA
ENST00000541113.6:c.538_540delinsGGA	ENSP00000442324.2:p.Gly180=
ENST00000679509.1:n.1500_1502delinsGGA
ENST00000679530.1:c.*306_*308delinsGGA	ENSP00000506454.1:n.*306_*308delinsGGA
ENST00000679615.1:n.2662_2664delinsGGA
ENST00000679687.1:c.100_102delinsGGA	ENSP00000506598.1:p.Gly34=
ENST00000679704.1:c.*304_*306delinsGGA	ENSP00000505117.1:n.*304_*306delinsGGA
ENST00000679709.1:c.*501_*503delinsGGA	ENSP00000506623.1:n.*501_*503delinsGGA
ENST00000679804.1:n.277_279delinsGGA
ENST00000679976.1:c.*122_*124delinsGGA	ENSP00000505565.1:n.*122_*124delinsGGA
ENST00000680166.1:n.3827_3829delinsGGA
ENST00000680517.1:c.*35_*37delinsGGA	ENSP00000505803.1:n.*35_*37delinsGGA
ENST00000680582.1:n.1500_1502delinsGGA
ENST00000680613.1:c.538_540delinsGGA	ENSP00000506114.1:p.Gly180=
ENST00000680662.1:c.*452_*454delinsGGA	ENSP00000505080.1:n.*452_*454delinsGGA
ENST00000680691.1:c.*201_*203delinsGGA	ENSP00000506487.1:n.*201_*203delinsGGA
ENST00000680694.1:c.*126_*128delinsGGA	ENSP00000505658.1:n.*126_*128delinsGGA
ENST00000680743.1:c.*205_*207delinsGGA	ENSP00000505073.1:n.*205_*207delinsGGA
ENST00000680749.1:c.538_540delinsGGA	ENSP00000505122.1:p.Gly180=
ENST00000680798.1:c.*122_*124delinsGGA	ENSP00000505670.1:n.*122_*124delinsGGA
ENST00000680805.1:c.538_540delinsGGA	ENSP00000505447.1:p.Gly180=
ENST00000680844.1:c.*322_*324delinsGGA	ENSP00000506541.1:n.*322_*324delinsGGA
ENST00000680948.1:c.*405_*407delinsGGA	ENSP00000505441.1:n.*405_*407delinsGGA
ENST00000680964.1:c.538_540delinsGGA	ENSP00000505961.1:p.Gly180=
ENST00000681037.1:c.538_540delinsGGA	ENSP00000506025.1:p.Gly180=
ENST00000681063.1:c.538_540delinsGGA	ENSP00000506616.1:p.Gly180=
ENST00000681209.1:c.*302_*304delinsGGA	ENSP00000505877.1:n.*302_*304delinsGGA
ENST00000681278.1:n.895_897delinsGGA
ENST00000681289.1:n.895_897delinsGGA
ENST00000681361.1:c.*205_*207delinsGGA	ENSP00000506679.1:n.*205_*207delinsGGA
ENST00000681430.1:c.538_540delinsGGA	ENSP00000506301.1:p.Gly180=
ENST00000681446.1:c.*120_*122delinsGGA	ENSP00000506244.1:n.*120_*122delinsGGA
ENST00000681450.1:c.*209_*211delinsGGA	ENSP00000505660.1:n.*209_*211delinsGGA
ENST00000681548.1:c.*124_*126delinsGGA	ENSP00000505275.1:n.*124_*126delinsGGA
ENST00000681616.1:c.*306_*308delinsGGA	ENSP00000505111.1:n.*306_*308delinsGGA
ENST00000681621.1:c.*122_*124delinsGGA	ENSP00000505770.1:n.*122_*124delinsGGA
ENST00000681680.1:n.2662_2664delinsGGA
ENST00000681720.1:c.*55-5757_*55-5755delinsGGA	ENSP00000505438.1:n.*55-5757_*55-5755delinsGGA
ENST00000681730.1:n.760_762delinsGGA
ENST00000681790.1:c.280_282delinsGGA	ENSP00000505130.1:p.Gly94=
ENST00000681837.1:n.1154_1156delinsGGA
ENST00000681913.1:n.2662_2664delinsGGA
ENST00000681916.1:c.*306_*308delinsGGA	ENSP00000506477.1:n.*306_*308delinsGGA
ENST00000681930.1:n.2662_2664delinsGGA
ENST00000370834.9:c.637_639delinsGGA	ENSP00000359871.5:p.Gly213=
ENST00000370841.8:c.538_540delinsGGA	ENSP00000359878.4:p.Gly180=
ENST00000420607.6:c.550_552delinsGGA	ENSP00000409612.2:p.Gly184=
ENST00000525808.5:c.*124_*126delinsGGA	ENSP00000434823.1:n.*124_*126delinsGGA
ENST00000526129.5:c.*322_*324delinsGGA	ENSP00000434092.1:n.*322_*324delinsGGA
ENST00000526196.5:c.*306_*308delinsGGA	ENSP00000431953.1:n.*306_*308delinsGGA
ENST00000526930.1:n.311_313delinsGGA
ENST00000529059.5:n.447_449delinsGGA
ENST00000530953.6:c.*35_*37delinsGGA	ENSP00000431372.1:n.*35_*37delinsGGA
ENST00000532509.5:c.*302_*304delinsGGA	ENSP00000432522.1:n.*302_*304delinsGGA
ENST00000534334.5:c.*122_*124delinsGGA	ENSP00000435584.1:n.*122_*124delinsGGA
ENST00000541113.5:c.430_432delinsGGA	ENSP00000442324.1:p.Gly144=
NM_000016.5:c.538_540delinsGGA	NP_000007.1:p.Gly180=
NM_001127328.2:c.550_552delinsGGA	NP_001120800.1:p.Gly184=
NM_001286042.1:c.430_432delinsGGA	NP_001272971.1:p.Gly144=
NM_001286043.1:c.637_639delinsGGA	NP_001272972.1:p.Gly213=
NM_001286044.1:c.-30_-28delinsGGA	NP_001272973.1:n.-30_-28delinsGGA
NM_000016.6:c.538_540delinsGGA MANE Select	NP_000007.1:p.Gly180=
NM_001127328.3:c.550_552delinsGGA	NP_001120800.1:p.Gly184=
NM_001286042.2:c.430_432delinsGGA	NP_001272971.1:p.Gly144=
NM_001286043.2:c.637_639delinsGGA	NP_001272972.1:p.Gly213=
NM_001286044.2:c.-30_-28delinsGGA	NP_001272973.1:n.-30_-28delinsGGA