Canonical Allele Identifier: CA340818138

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226946G>T (hg19) ; chr1:g.75761261G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761261G>T , CM000663.2:g.75761261G>T	GRCh38
NC_000001.10:g.76226946G>T , CM000663.1:g.76226946G>T	GRCh37
NC_000001.9:g.75999534G>T	NCBI36
NG_007045.2:g.41904G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.1085G>T MANE Select	ENSP00000359878.5:p.Gly362Val
ENST00000473018.3:n.3209G>T
ENST00000532207.6:n.2096G>T
ENST00000541113.6:c.989G>T	ENSP00000442324.2:p.Gly330Val
ENST00000679509.1:n.2047G>T
ENST00000679530.1:c.*853G>T	ENSP00000506454.1:n.*853G>T
ENST00000679615.1:n.3100G>T
ENST00000679687.1:c.647G>T	ENSP00000506598.1:p.Gly216Val
ENST00000679704.1:c.*851G>T	ENSP00000505117.1:n.*851G>T
ENST00000679709.1:c.*1048G>T	ENSP00000506623.1:n.*1048G>T
ENST00000679976.1:c.*669G>T	ENSP00000505565.1:n.*669G>T
ENST00000680166.1:n.4374G>T
ENST00000680315.1:n.968G>T
ENST00000680517.1:c.*473G>T	ENSP00000505803.1:n.*473G>T
ENST00000680582.1:n.2047G>T
ENST00000680613.1:c.*578G>T	ENSP00000506114.1:n.*578G>T
ENST00000680662.1:c.*999G>T	ENSP00000505080.1:n.*999G>T
ENST00000680691.1:c.*748G>T	ENSP00000506487.1:n.*748G>T
ENST00000680694.1:c.*673G>T	ENSP00000505658.1:n.*673G>T
ENST00000680743.1:c.*874G>T	ENSP00000505073.1:n.*874G>T
ENST00000680749.1:c.*370G>T	ENSP00000505122.1:n.*370G>T
ENST00000680798.1:c.*560G>T	ENSP00000505670.1:n.*560G>T
ENST00000680805.1:c.944G>T	ENSP00000505447.1:p.Gly315Val
ENST00000680844.1:c.*869G>T	ENSP00000506541.1:n.*869G>T
ENST00000680948.1:c.*952G>T	ENSP00000505441.1:n.*952G>T
ENST00000680964.1:c.*178G>T	ENSP00000505961.1:n.*178G>T
ENST00000681037.1:c.*2569G>T	ENSP00000506025.1:n.*2569G>T
ENST00000681063.1:c.*354G>T	ENSP00000506616.1:n.*354G>T
ENST00000681209.1:c.*740G>T	ENSP00000505877.1:n.*740G>T
ENST00000681278.1:n.1787G>T
ENST00000681289.1:n.5080G>T
ENST00000681361.1:c.*752G>T	ENSP00000506679.1:n.*752G>T
ENST00000681430.1:c.*178G>T	ENSP00000506301.1:n.*178G>T
ENST00000681446.1:c.*789G>T	ENSP00000506244.1:n.*789G>T
ENST00000681450.1:c.*756G>T	ENSP00000505660.1:n.*756G>T
ENST00000681548.1:c.*671G>T	ENSP00000505275.1:n.*671G>T
ENST00000681616.1:c.*744G>T	ENSP00000505111.1:n.*744G>T
ENST00000681621.1:c.*669G>T	ENSP00000505770.1:n.*669G>T
ENST00000681680.1:n.3180G>T
ENST00000681720.1:c.*540G>T	ENSP00000505438.1:n.*540G>T
ENST00000681730.1:n.1307G>T
ENST00000681790.1:c.827G>T	ENSP00000505130.1:p.Gly276Val
ENST00000681837.1:n.1701G>T
ENST00000681913.1:n.3331G>T
ENST00000681916.1:c.*853G>T	ENSP00000506477.1:n.*853G>T
ENST00000681930.1:n.3209G>T
ENST00000370834.9:c.1184G>T	ENSP00000359871.5:p.Gly395Val
ENST00000370841.8:c.1085G>T	ENSP00000359878.4:p.Gly362Val
ENST00000420607.6:c.1097G>T	ENSP00000409612.2:p.Gly366Val
ENST00000481374.1:n.358G>T
ENST00000525808.5:c.*671G>T	ENSP00000434823.1:n.*671G>T
ENST00000526129.5:c.*869G>T	ENSP00000434092.1:n.*869G>T
ENST00000526196.5:c.*853G>T	ENSP00000431953.1:n.*853G>T
ENST00000528016.1:c.160-7916G>T	ENSP00000434284.1:n.160-7916G>T
ENST00000529059.5:n.994G>T
ENST00000541113.5:c.977G>T	ENSP00000442324.1:p.Gly326Val
NM_000016.5:c.1085G>T	NP_000007.1:p.Gly362Val
NM_001127328.2:c.1097G>T	NP_001120800.1:p.Gly366Val
NM_001286042.1:c.977G>T	NP_001272971.1:p.Gly326Val
NM_001286043.1:c.1184G>T	NP_001272972.1:p.Gly395Val
NM_001286044.1:c.518G>T	NP_001272973.1:p.Gly173Val
NM_000016.6:c.1085G>T MANE Select	NP_000007.1:p.Gly362Val
NM_001127328.3:c.1097G>T	NP_001120800.1:p.Gly366Val
NM_001286042.2:c.977G>T	NP_001272971.1:p.Gly326Val
NM_001286043.2:c.1184G>T	NP_001272972.1:p.Gly395Val
NM_001286044.2:c.518G>T	NP_001272973.1:p.Gly173Val