Canonical Allele Identifier: CA1176726832
Gene: ACADM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75761200_75761201delinsTG , CM000663.2:g.75761200_75761201delinsTG GRCh38
NC_000001.10:g.76226885_76226886delinsTG , CM000663.1:g.76226885_76226886delinsTG GRCh37
NC_000001.9:g.75999473_75999474delinsTG NCBI36
NG_007045.2:g.41843_41844delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000370841.9:c.1024_1025delinsTG MANE Select ENSP00000359878.5:p.Trp342=
ENST00000473018.3:n.3148_3149delinsTG
ENST00000532207.6:n.2035_2036delinsTG
ENST00000541113.6:c.928_929delinsTG ENSP00000442324.2:p.Trp310=
ENST00000679509.1:n.1986_1987delinsTG
ENST00000679530.1:c.*792_*793delinsTG ENSP00000506454.1:n.*792_*793delinsTG
ENST00000679615.1:n.3039_3040delinsTG
ENST00000679687.1:c.586_587delinsTG ENSP00000506598.1:p.Trp196=
ENST00000679704.1:c.*790_*791delinsTG ENSP00000505117.1:n.*790_*791delinsTG
ENST00000679709.1:c.*987_*988delinsTG ENSP00000506623.1:n.*987_*988delinsTG
ENST00000679976.1:c.*608_*609delinsTG ENSP00000505565.1:n.*608_*609delinsTG
ENST00000680166.1:n.4313_4314delinsTG
ENST00000680315.1:n.907_908delinsTG
ENST00000680517.1:c.*412_*413delinsTG ENSP00000505803.1:n.*412_*413delinsTG
ENST00000680582.1:n.1986_1987delinsTG
ENST00000680613.1:c.*517_*518delinsTG ENSP00000506114.1:n.*517_*518delinsTG
ENST00000680662.1:c.*938_*939delinsTG ENSP00000505080.1:n.*938_*939delinsTG
ENST00000680691.1:c.*687_*688delinsTG ENSP00000506487.1:n.*687_*688delinsTG
ENST00000680694.1:c.*612_*613delinsTG ENSP00000505658.1:n.*612_*613delinsTG
ENST00000680743.1:c.*813_*814delinsTG ENSP00000505073.1:n.*813_*814delinsTG
ENST00000680749.1:c.*309_*310delinsTG ENSP00000505122.1:n.*309_*310delinsTG
ENST00000680798.1:c.*499_*500delinsTG ENSP00000505670.1:n.*499_*500delinsTG
ENST00000680805.1:c.883_884delinsTG ENSP00000505447.1:p.Trp295=
ENST00000680844.1:c.*808_*809delinsTG ENSP00000506541.1:n.*808_*809delinsTG
ENST00000680948.1:c.*891_*892delinsTG ENSP00000505441.1:n.*891_*892delinsTG
ENST00000680964.1:c.*117_*118delinsTG ENSP00000505961.1:n.*117_*118delinsTG
ENST00000681037.1:c.*2508_*2509delinsTG ENSP00000506025.1:n.*2508_*2509delinsTG
ENST00000681063.1:c.*293_*294delinsTG ENSP00000506616.1:n.*293_*294delinsTG
ENST00000681209.1:c.*679_*680delinsTG ENSP00000505877.1:n.*679_*680delinsTG
ENST00000681278.1:n.1726_1727delinsTG
ENST00000681289.1:n.5019_5020delinsTG
ENST00000681361.1:c.*691_*692delinsTG ENSP00000506679.1:n.*691_*692delinsTG
ENST00000681430.1:c.*117_*118delinsTG ENSP00000506301.1:n.*117_*118delinsTG
ENST00000681446.1:c.*728_*729delinsTG ENSP00000506244.1:n.*728_*729delinsTG
ENST00000681450.1:c.*695_*696delinsTG ENSP00000505660.1:n.*695_*696delinsTG
ENST00000681548.1:c.*610_*611delinsTG ENSP00000505275.1:n.*610_*611delinsTG
ENST00000681616.1:c.*683_*684delinsTG ENSP00000505111.1:n.*683_*684delinsTG
ENST00000681621.1:c.*608_*609delinsTG ENSP00000505770.1:n.*608_*609delinsTG
ENST00000681680.1:n.3119_3120delinsTG
ENST00000681720.1:c.*479_*480delinsTG ENSP00000505438.1:n.*479_*480delinsTG
ENST00000681730.1:n.1246_1247delinsTG
ENST00000681790.1:c.766_767delinsTG ENSP00000505130.1:p.Trp256=
ENST00000681837.1:n.1640_1641delinsTG
ENST00000681913.1:n.3270_3271delinsTG
ENST00000681916.1:c.*792_*793delinsTG ENSP00000506477.1:n.*792_*793delinsTG
ENST00000681930.1:n.3148_3149delinsTG
ENST00000370834.9:c.1123_1124delinsTG ENSP00000359871.5:p.Trp375=
ENST00000370841.8:c.1024_1025delinsTG ENSP00000359878.4:p.Trp342=
ENST00000420607.6:c.1036_1037delinsTG ENSP00000409612.2:p.Trp346=
ENST00000481374.1:n.297_298delinsTG
ENST00000525808.5:c.*610_*611delinsTG ENSP00000434823.1:n.*610_*611delinsTG
ENST00000526129.5:c.*808_*809delinsTG ENSP00000434092.1:n.*808_*809delinsTG
ENST00000526196.5:c.*792_*793delinsTG ENSP00000431953.1:n.*792_*793delinsTG
ENST00000528016.1:c.160-7977_160-7976delinsTG ENSP00000434284.1:n.160-7977_160-7976deli...
ENST00000529059.5:n.933_934delinsTG
ENST00000532207.5:n.754_755delinsTG
ENST00000534334.5:c.*765_*766delinsTG ENSP00000435584.1:n.*765_*766delinsTG
ENST00000541113.5:c.916_917delinsTG ENSP00000442324.1:p.Trp306=
NM_000016.5:c.1024_1025delinsTG NP_000007.1:p.Trp342=
NM_001127328.2:c.1036_1037delinsTG NP_001120800.1:p.Trp346=
NM_001286042.1:c.916_917delinsTG NP_001272971.1:p.Trp306=
NM_001286043.1:c.1123_1124delinsTG NP_001272972.1:p.Trp375=
NM_001286044.1:c.457_458delinsTG NP_001272973.1:p.Trp153=
NM_000016.6:c.1024_1025delinsTG MANE Select NP_000007.1:p.Trp342=
NM_001127328.3:c.1036_1037delinsTG NP_001120800.1:p.Trp346=
NM_001286042.2:c.916_917delinsTG NP_001272971.1:p.Trp306=
NM_001286043.2:c.1123_1124delinsTG NP_001272972.1:p.Trp375=
NM_001286044.2:c.457_458delinsTG NP_001272973.1:p.Trp153=