Canonical Allele Identifier: CA340818372

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76227056G>T (hg19) ; chr1:g.75761371G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761371G>T , CM000663.2:g.75761371G>T	GRCh38
NC_000001.10:g.76227056G>T , CM000663.1:g.76227056G>T	GRCh37
NC_000001.9:g.75999644G>T	NCBI36
NG_007045.2:g.42014G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.1194+1G>T MANE Select	ENSP00000359878.5:n.1194+1G>T
ENST00000473018.3:n.3318+1G>T
ENST00000532207.6:n.2206G>T
ENST00000541113.6:c.1098+1G>T	ENSP00000442324.2:n.1098+1G>T
ENST00000679509.1:n.2157G>T
ENST00000679530.1:c.*962+1G>T	ENSP00000506454.1:n.*962+1G>T
ENST00000679615.1:n.3210G>T
ENST00000679687.1:c.756+1G>T	ENSP00000506598.1:n.756+1G>T
ENST00000679704.1:c.*960+1G>T	ENSP00000505117.1:n.*960+1G>T
ENST00000679709.1:c.*1157+1G>T	ENSP00000506623.1:n.*1157+1G>T
ENST00000679976.1:c.*778+1G>T	ENSP00000505565.1:n.*778+1G>T
ENST00000680166.1:n.4483+1G>T
ENST00000680315.1:n.1078G>T
ENST00000680517.1:c.*583G>T	ENSP00000505803.1:n.*583G>T
ENST00000680582.1:n.2156+1G>T
ENST00000680613.1:c.*687+1G>T	ENSP00000506114.1:n.*687+1G>T
ENST00000680662.1:c.*1108+1G>T	ENSP00000505080.1:n.*1108+1G>T
ENST00000680691.1:c.*857+1G>T	ENSP00000506487.1:n.*857+1G>T
ENST00000680694.1:c.*782+1G>T	ENSP00000505658.1:n.*782+1G>T
ENST00000680743.1:c.*983+1G>T	ENSP00000505073.1:n.*983+1G>T
ENST00000680749.1:c.*479+1G>T	ENSP00000505122.1:n.*479+1G>T
ENST00000680798.1:c.*670G>T	ENSP00000505670.1:n.*670G>T
ENST00000680805.1:c.1053+1G>T	ENSP00000505447.1:n.1053+1G>T
ENST00000680844.1:c.*979G>T	ENSP00000506541.1:n.*979G>T
ENST00000680948.1:c.*1061+1G>T	ENSP00000505441.1:n.*1061+1G>T
ENST00000680964.1:c.*288G>T	ENSP00000505961.1:n.*288G>T
ENST00000681037.1:c.*2678+1G>T	ENSP00000506025.1:n.*2678+1G>T
ENST00000681063.1:c.*463+1G>T	ENSP00000506616.1:n.*463+1G>T
ENST00000681209.1:c.*849+1G>T	ENSP00000505877.1:n.*849+1G>T
ENST00000681278.1:n.1896+1G>T
ENST00000681289.1:n.5189+1G>T
ENST00000681361.1:c.*862G>T	ENSP00000506679.1:n.*862G>T
ENST00000681430.1:c.*287+1G>T	ENSP00000506301.1:n.*287+1G>T
ENST00000681446.1:c.*899G>T	ENSP00000506244.1:n.*899G>T
ENST00000681450.1:c.*865+1G>T	ENSP00000505660.1:n.*865+1G>T
ENST00000681548.1:c.*781G>T	ENSP00000505275.1:n.*781G>T
ENST00000681616.1:c.*854G>T	ENSP00000505111.1:n.*854G>T
ENST00000681621.1:c.*779G>T	ENSP00000505770.1:n.*779G>T
ENST00000681680.1:n.3290G>T
ENST00000681720.1:c.*649+1G>T	ENSP00000505438.1:n.*649+1G>T
ENST00000681730.1:n.1416+1G>T
ENST00000681790.1:c.936+1G>T	ENSP00000505130.1:n.936+1G>T
ENST00000681837.1:n.1811G>T
ENST00000681913.1:n.3440+1G>T
ENST00000681916.1:c.*962+1G>T	ENSP00000506477.1:n.*962+1G>T
ENST00000681930.1:n.3319G>T
ENST00000370834.9:c.1293+1G>T	ENSP00000359871.5:n.1293+1G>T
ENST00000370841.8:c.1194+1G>T	ENSP00000359878.4:n.1194+1G>T
ENST00000420607.6:c.1206+1G>T	ENSP00000409612.2:n.1206+1G>T
ENST00000481374.1:n.467+1G>T
ENST00000525808.5:c.*780+1G>T	ENSP00000434823.1:n.*780+1G>T
ENST00000526129.5:c.*979G>T	ENSP00000434092.1:n.*979G>T
ENST00000526196.5:c.*962+1G>T	ENSP00000431953.1:n.*962+1G>T
ENST00000528016.1:c.160-7806G>T	ENSP00000434284.1:n.160-7806G>T
ENST00000529059.5:n.1103+1G>T
ENST00000541113.5:c.1086+1G>T	ENSP00000442324.1:n.1086+1G>T
NM_000016.5:c.1194+1G>T	NP_000007.1:n.1194+1G>T
NM_001127328.2:c.1206+1G>T	NP_001120800.1:n.1206+1G>T
NM_001286042.1:c.1086+1G>T	NP_001272971.1:n.1086+1G>T
NM_001286043.1:c.1293+1G>T	NP_001272972.1:n.1293+1G>T
NM_001286044.1:c.627+1G>T	NP_001272973.1:n.627+1G>T
NM_000016.6:c.1194+1G>T MANE Select	NP_000007.1:n.1194+1G>T
NM_001127328.3:c.1206+1G>T	NP_001120800.1:n.1206+1G>T
NM_001286042.2:c.1086+1G>T	NP_001272971.1:n.1086+1G>T
NM_001286043.2:c.1293+1G>T	NP_001272972.1:n.1293+1G>T
NM_001286044.2:c.627+1G>T	NP_001272973.1:n.627+1G>T