Canonical Allele Identifier: CA1176726815
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761159_75761160delinsTG , CM000663.2:g.75761159_75761160delinsTG GRCh38
NC_000001.10:g.76226844_76226845delinsTG , CM000663.1:g.76226844_76226845delinsTG GRCh37
NC_000001.9:g.75999432_75999433delinsTG NCBI36
NG_007045.2:g.41802_41803delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.983_984delinsTG MANE Select ENSP00000359878.5:p.Met328=
ENST00000473018.3:n.3107_3108delinsTG
ENST00000532207.6:n.1994_1995delinsTG
ENST00000541113.6:c.887_888delinsTG ENSP00000442324.2:p.Met296=
ENST00000679509.1:n.1945_1946delinsTG
ENST00000679530.1:c.*751_*752delinsTG ENSP00000506454.1:n.*751_*752delinsTG
ENST00000679615.1:n.2998_2999delinsTG
ENST00000679687.1:c.545_546delinsTG ENSP00000506598.1:p.Met182=
ENST00000679704.1:c.*749_*750delinsTG ENSP00000505117.1:n.*749_*750delinsTG
ENST00000679709.1:c.*946_*947delinsTG ENSP00000506623.1:n.*946_*947delinsTG
ENST00000679976.1:c.*567_*568delinsTG ENSP00000505565.1:n.*567_*568delinsTG
ENST00000680166.1:n.4272_4273delinsTG
ENST00000680315.1:n.866_867delinsTG
ENST00000680517.1:c.*371_*372delinsTG ENSP00000505803.1:n.*371_*372delinsTG
ENST00000680582.1:n.1945_1946delinsTG
ENST00000680613.1:c.*476_*477delinsTG ENSP00000506114.1:n.*476_*477delinsTG
ENST00000680662.1:c.*897_*898delinsTG ENSP00000505080.1:n.*897_*898delinsTG
ENST00000680691.1:c.*646_*647delinsTG ENSP00000506487.1:n.*646_*647delinsTG
ENST00000680694.1:c.*571_*572delinsTG ENSP00000505658.1:n.*571_*572delinsTG
ENST00000680743.1:c.*772_*773delinsTG ENSP00000505073.1:n.*772_*773delinsTG
ENST00000680749.1:c.*268_*269delinsTG ENSP00000505122.1:n.*268_*269delinsTG
ENST00000680798.1:c.*458_*459delinsTG ENSP00000505670.1:n.*458_*459delinsTG
ENST00000680805.1:c.842_843delinsTG ENSP00000505447.1:p.Met281=
ENST00000680844.1:c.*767_*768delinsTG ENSP00000506541.1:n.*767_*768delinsTG
ENST00000680948.1:c.*850_*851delinsTG ENSP00000505441.1:n.*850_*851delinsTG
ENST00000680964.1:c.*76_*77delinsTG ENSP00000505961.1:n.*76_*77delinsTG
ENST00000681037.1:c.*2467_*2468delinsTG ENSP00000506025.1:n.*2467_*2468delinsTG
ENST00000681063.1:c.*252_*253delinsTG ENSP00000506616.1:n.*252_*253delinsTG
ENST00000681209.1:c.*638_*639delinsTG ENSP00000505877.1:n.*638_*639delinsTG
ENST00000681278.1:n.1685_1686delinsTG
ENST00000681289.1:n.4978_4979delinsTG
ENST00000681361.1:c.*650_*651delinsTG ENSP00000506679.1:n.*650_*651delinsTG
ENST00000681430.1:c.*76_*77delinsTG ENSP00000506301.1:n.*76_*77delinsTG
ENST00000681446.1:c.*687_*688delinsTG ENSP00000506244.1:n.*687_*688delinsTG
ENST00000681450.1:c.*654_*655delinsTG ENSP00000505660.1:n.*654_*655delinsTG
ENST00000681548.1:c.*569_*570delinsTG ENSP00000505275.1:n.*569_*570delinsTG
ENST00000681616.1:c.*642_*643delinsTG ENSP00000505111.1:n.*642_*643delinsTG
ENST00000681621.1:c.*567_*568delinsTG ENSP00000505770.1:n.*567_*568delinsTG
ENST00000681680.1:n.3078_3079delinsTG
ENST00000681720.1:c.*438_*439delinsTG ENSP00000505438.1:n.*438_*439delinsTG
ENST00000681730.1:n.1205_1206delinsTG
ENST00000681790.1:c.725_726delinsTG ENSP00000505130.1:p.Met242=
ENST00000681837.1:n.1599_1600delinsTG
ENST00000681913.1:n.3229_3230delinsTG
ENST00000681916.1:c.*751_*752delinsTG ENSP00000506477.1:n.*751_*752delinsTG
ENST00000681930.1:n.3107_3108delinsTG
ENST00000370834.9:c.1082_1083delinsTG ENSP00000359871.5:p.Met361=
ENST00000370841.8:c.983_984delinsTG ENSP00000359878.4:p.Met328=
ENST00000420607.6:c.995_996delinsTG ENSP00000409612.2:p.Met332=
ENST00000481374.1:n.256_257delinsTG
ENST00000525808.5:c.*569_*570delinsTG ENSP00000434823.1:n.*569_*570delinsTG
ENST00000526129.5:c.*767_*768delinsTG ENSP00000434092.1:n.*767_*768delinsTG
ENST00000526196.5:c.*751_*752delinsTG ENSP00000431953.1:n.*751_*752delinsTG
ENST00000528016.1:c.160-8018_160-8017delinsTG ENSP00000434284.1:n.160-8018_160-8017delinsTG
ENST00000529059.5:n.892_893delinsTG
ENST00000532207.5:n.713_714delinsTG
ENST00000534334.5:c.*724_*725delinsTG ENSP00000435584.1:n.*724_*725delinsTG
ENST00000541113.5:c.875_876delinsTG ENSP00000442324.1:p.Met292=
NM_000016.5:c.983_984delinsTG NP_000007.1:p.Met328=
NM_001127328.2:c.995_996delinsTG NP_001120800.1:p.Met332=
NM_001286042.1:c.875_876delinsTG NP_001272971.1:p.Met292=
NM_001286043.1:c.1082_1083delinsTG NP_001272972.1:p.Met361=
NM_001286044.1:c.416_417delinsTG NP_001272973.1:p.Met139=
NM_000016.6:c.983_984delinsTG MANE Select NP_000007.1:p.Met328=
NM_001127328.3:c.995_996delinsTG NP_001120800.1:p.Met332=
NM_001286042.2:c.875_876delinsTG NP_001272971.1:p.Met292=
NM_001286043.2:c.1082_1083delinsTG NP_001272972.1:p.Met361=
NM_001286044.2:c.416_417delinsTG NP_001272973.1:p.Met139=