Canonical Allele Identifier: CA916210465
Gene: ACADM HGNC NCBI

Linked Data

dbSNP Id: rs1570910313

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761304_75761305insTC , CM000663.2:g.75761304_75761305insTC GRCh38
NC_000001.10:g.76226989_76226990insTC , CM000663.1:g.76226989_76226990insTC GRCh37
NC_000001.9:g.75999577_75999578insTC NCBI36
NG_007045.2:g.41947_41948insTC

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1128_1129insTC MANE Select ENSP00000359878.5:p.Gly377SerfsTer12
ENST00000473018.3:n.3252_3253insTC
ENST00000532207.6:n.2139_2140insTC
ENST00000541113.6:c.1032_1033insTC ENSP00000442324.2:p.Gly345SerfsTer12
ENST00000679509.1:n.2090_2091insTC
ENST00000679530.1:c.*896_*897insTC ENSP00000506454.1:n.*896_*897insTC
ENST00000679615.1:n.3143_3144insTC
ENST00000679687.1:c.690_691insTC ENSP00000506598.1:p.Gly231SerfsTer12
ENST00000679704.1:c.*894_*895insTC ENSP00000505117.1:n.*894_*895insTC
ENST00000679709.1:c.*1091_*1092insTC ENSP00000506623.1:n.*1091_*1092insTC
ENST00000679976.1:c.*712_*713insTC ENSP00000505565.1:n.*712_*713insTC
ENST00000680166.1:n.4417_4418insTC
ENST00000680315.1:n.1011_1012insTC
ENST00000680517.1:c.*516_*517insTC ENSP00000505803.1:n.*516_*517insTC
ENST00000680582.1:n.2090_2091insTC
ENST00000680613.1:c.*621_*622insTC ENSP00000506114.1:n.*621_*622insTC
ENST00000680662.1:c.*1042_*1043insTC ENSP00000505080.1:n.*1042_*1043insTC
ENST00000680691.1:c.*791_*792insTC ENSP00000506487.1:n.*791_*792insTC
ENST00000680694.1:c.*716_*717insTC ENSP00000505658.1:n.*716_*717insTC
ENST00000680743.1:c.*917_*918insTC ENSP00000505073.1:n.*917_*918insTC
ENST00000680749.1:c.*413_*414insTC ENSP00000505122.1:n.*413_*414insTC
ENST00000680798.1:c.*603_*604insTC ENSP00000505670.1:n.*603_*604insTC
ENST00000680805.1:c.987_988insTC ENSP00000505447.1:p.Gly330SerfsTer12
ENST00000680844.1:c.*912_*913insTC ENSP00000506541.1:n.*912_*913insTC
ENST00000680948.1:c.*995_*996insTC ENSP00000505441.1:n.*995_*996insTC
ENST00000680964.1:c.*221_*222insTC ENSP00000505961.1:n.*221_*222insTC
ENST00000681037.1:c.*2612_*2613insTC ENSP00000506025.1:n.*2612_*2613insTC
ENST00000681063.1:c.*397_*398insTC ENSP00000506616.1:n.*397_*398insTC
ENST00000681209.1:c.*783_*784insTC ENSP00000505877.1:n.*783_*784insTC
ENST00000681278.1:n.1830_1831insTC
ENST00000681289.1:n.5123_5124insTC
ENST00000681361.1:c.*795_*796insTC ENSP00000506679.1:n.*795_*796insTC
ENST00000681430.1:c.*221_*222insTC ENSP00000506301.1:n.*221_*222insTC
ENST00000681446.1:c.*832_*833insTC ENSP00000506244.1:n.*832_*833insTC
ENST00000681450.1:c.*799_*800insTC ENSP00000505660.1:n.*799_*800insTC
ENST00000681548.1:c.*714_*715insTC ENSP00000505275.1:n.*714_*715insTC
ENST00000681616.1:c.*787_*788insTC ENSP00000505111.1:n.*787_*788insTC
ENST00000681621.1:c.*712_*713insTC ENSP00000505770.1:n.*712_*713insTC
ENST00000681680.1:n.3223_3224insTC
ENST00000681720.1:c.*583_*584insTC ENSP00000505438.1:n.*583_*584insTC
ENST00000681730.1:n.1350_1351insTC
ENST00000681790.1:c.870_871insTC ENSP00000505130.1:p.Gly291SerfsTer12
ENST00000681837.1:n.1744_1745insTC
ENST00000681913.1:n.3374_3375insTC
ENST00000681916.1:c.*896_*897insTC ENSP00000506477.1:n.*896_*897insTC
ENST00000681930.1:n.3252_3253insTC
ENST00000370834.9:c.1227_1228insTC ENSP00000359871.5:p.Gly410SerfsTer12
ENST00000370841.8:c.1128_1129insTC ENSP00000359878.4:p.Gly377SerfsTer12
ENST00000420607.6:c.1140_1141insTC ENSP00000409612.2:p.Gly381SerfsTer12
ENST00000481374.1:n.401_402insTC
ENST00000525808.5:c.*714_*715insTC ENSP00000434823.1:n.*714_*715insTC
ENST00000526129.5:c.*912_*913insTC ENSP00000434092.1:n.*912_*913insTC
ENST00000526196.5:c.*896_*897insTC ENSP00000431953.1:n.*896_*897insTC
ENST00000528016.1:c.160-7873_160-7872insTC ENSP00000434284.1:n.160-7873_160-7872insT...
ENST00000529059.5:n.1037_1038insTC
ENST00000541113.5:c.1020_1021insTC ENSP00000442324.1:p.Gly341SerfsTer12
NM_000016.5:c.1128_1129insTC NP_000007.1:p.Gly377SerfsTer12
NM_001127328.2:c.1140_1141insTC NP_001120800.1:p.Gly381SerfsTer12
NM_001286042.1:c.1020_1021insTC NP_001272971.1:p.Gly341SerfsTer12
NM_001286043.1:c.1227_1228insTC NP_001272972.1:p.Gly410SerfsTer12
NM_001286044.1:c.561_562insTC NP_001272973.1:p.Gly188SerfsTer12
NM_000016.6:c.1128_1129insTC MANE Select NP_000007.1:p.Gly377SerfsTer12
NM_001127328.3:c.1140_1141insTC NP_001120800.1:p.Gly381SerfsTer12
NM_001286042.2:c.1020_1021insTC NP_001272971.1:p.Gly341SerfsTer12
NM_001286043.2:c.1227_1228insTC NP_001272972.1:p.Gly410SerfsTer12
NM_001286044.2:c.561_562insTC NP_001272973.1:p.Gly188SerfsTer12