Canonical Allele Identifier: CA738877785

Gene: ACADM

Linked Data

• dbSNP Id: rs1284761061
• MyVariant Identifiers: chr1:g.76227070G>T (hg19) ; chr1:g.75761385G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761385G>T , CM000663.2:g.75761385G>T	GRCh38
NC_000001.10:g.76227070G>T , CM000663.1:g.76227070G>T	GRCh37
NC_000001.9:g.75999658G>T	NCBI36
NG_007045.2:g.42028G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.1194+15G>T MANE Select	ENSP00000359878.5:n.1194+15G>T
ENST00000473018.3:n.3318+15G>T
ENST00000532207.6:n.2220G>T
ENST00000541113.6:c.1098+15G>T	ENSP00000442324.2:n.1098+15G>T
ENST00000679509.1:n.2171G>T
ENST00000679530.1:c.*962+15G>T	ENSP00000506454.1:n.*962+15G>T
ENST00000679615.1:n.3224G>T
ENST00000679687.1:c.756+15G>T	ENSP00000506598.1:n.756+15G>T
ENST00000679704.1:c.*960+15G>T	ENSP00000505117.1:n.*960+15G>T
ENST00000679709.1:c.*1157+15G>T	ENSP00000506623.1:n.*1157+15G>T
ENST00000679976.1:c.*778+15G>T	ENSP00000505565.1:n.*778+15G>T
ENST00000680166.1:n.4483+15G>T
ENST00000680315.1:n.1092G>T
ENST00000680517.1:c.*597G>T	ENSP00000505803.1:n.*597G>T
ENST00000680582.1:n.2156+15G>T
ENST00000680613.1:c.*687+15G>T	ENSP00000506114.1:n.*687+15G>T
ENST00000680662.1:c.*1108+15G>T	ENSP00000505080.1:n.*1108+15G>T
ENST00000680691.1:c.*857+15G>T	ENSP00000506487.1:n.*857+15G>T
ENST00000680694.1:c.*782+15G>T	ENSP00000505658.1:n.*782+15G>T
ENST00000680743.1:c.*983+15G>T	ENSP00000505073.1:n.*983+15G>T
ENST00000680749.1:c.*479+15G>T	ENSP00000505122.1:n.*479+15G>T
ENST00000680798.1:c.*684G>T	ENSP00000505670.1:n.*684G>T
ENST00000680805.1:c.1053+15G>T	ENSP00000505447.1:n.1053+15G>T
ENST00000680844.1:c.*993G>T	ENSP00000506541.1:n.*993G>T
ENST00000680948.1:c.*1061+15G>T	ENSP00000505441.1:n.*1061+15G>T
ENST00000680964.1:c.*302G>T	ENSP00000505961.1:n.*302G>T
ENST00000681037.1:c.*2678+15G>T	ENSP00000506025.1:n.*2678+15G>T
ENST00000681063.1:c.*463+15G>T	ENSP00000506616.1:n.*463+15G>T
ENST00000681209.1:c.*849+15G>T	ENSP00000505877.1:n.*849+15G>T
ENST00000681278.1:n.1896+15G>T
ENST00000681289.1:n.5189+15G>T
ENST00000681361.1:c.*876G>T	ENSP00000506679.1:n.*876G>T
ENST00000681430.1:c.*287+15G>T	ENSP00000506301.1:n.*287+15G>T
ENST00000681446.1:c.*913G>T	ENSP00000506244.1:n.*913G>T
ENST00000681450.1:c.*865+15G>T	ENSP00000505660.1:n.*865+15G>T
ENST00000681548.1:c.*795G>T	ENSP00000505275.1:n.*795G>T
ENST00000681616.1:c.*868G>T	ENSP00000505111.1:n.*868G>T
ENST00000681621.1:c.*793G>T	ENSP00000505770.1:n.*793G>T
ENST00000681680.1:n.3304G>T
ENST00000681720.1:c.*649+15G>T	ENSP00000505438.1:n.*649+15G>T
ENST00000681730.1:n.1416+15G>T
ENST00000681790.1:c.936+15G>T	ENSP00000505130.1:n.936+15G>T
ENST00000681837.1:n.1825G>T
ENST00000681913.1:n.3440+15G>T
ENST00000681916.1:c.*962+15G>T	ENSP00000506477.1:n.*962+15G>T
ENST00000681930.1:n.3333G>T
ENST00000370834.9:c.1293+15G>T	ENSP00000359871.5:n.1293+15G>T
ENST00000370841.8:c.1194+15G>T	ENSP00000359878.4:n.1194+15G>T
ENST00000420607.6:c.1206+15G>T	ENSP00000409612.2:n.1206+15G>T
ENST00000481374.1:n.467+15G>T
ENST00000525808.5:c.*780+15G>T	ENSP00000434823.1:n.*780+15G>T
ENST00000526129.5:c.*993G>T	ENSP00000434092.1:n.*993G>T
ENST00000526196.5:c.*962+15G>T	ENSP00000431953.1:n.*962+15G>T
ENST00000528016.1:c.160-7792G>T	ENSP00000434284.1:n.160-7792G>T
ENST00000529059.5:n.1103+15G>T
ENST00000541113.5:c.1086+15G>T	ENSP00000442324.1:n.1086+15G>T
NM_000016.5:c.1194+15G>T	NP_000007.1:n.1194+15G>T
NM_001127328.2:c.1206+15G>T	NP_001120800.1:n.1206+15G>T
NM_001286042.1:c.1086+15G>T	NP_001272971.1:n.1086+15G>T
NM_001286043.1:c.1293+15G>T	NP_001272972.1:n.1293+15G>T
NM_001286044.1:c.627+15G>T	NP_001272973.1:n.627+15G>T
NM_000016.6:c.1194+15G>T MANE Select	NP_000007.1:n.1194+15G>T
NM_001127328.3:c.1206+15G>T	NP_001120800.1:n.1206+15G>T
NM_001286042.2:c.1086+15G>T	NP_001272971.1:n.1086+15G>T
NM_001286043.2:c.1293+15G>T	NP_001272972.1:n.1293+15G>T
NM_001286044.2:c.627+15G>T	NP_001272973.1:n.627+15G>T