Canonical Allele Identifier: CA418707783

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76227019T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761334T>G , CM000663.2:g.75761334T>G	GRCh38
NC_000001.10:g.76227019T>G , CM000663.1:g.76227019T>G	GRCh37
NC_000001.9:g.75999607T>G	NCBI36
NG_007045.2:g.41977T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.1158T>G MANE Select	ENSP00000359878.5:p.Pro386=
ENST00000473018.3:n.3282T>G
ENST00000532207.6:n.2169T>G
ENST00000541113.6:c.1062T>G	ENSP00000442324.2:p.Pro354=
ENST00000679509.1:n.2120T>G
ENST00000679530.1:c.*926T>G	ENSP00000506454.1:n.*926T>G
ENST00000679615.1:n.3173T>G
ENST00000679687.1:c.720T>G	ENSP00000506598.1:p.Pro240=
ENST00000679704.1:c.*924T>G	ENSP00000505117.1:n.*924T>G
ENST00000679709.1:c.*1121T>G	ENSP00000506623.1:n.*1121T>G
ENST00000679976.1:c.*742T>G	ENSP00000505565.1:n.*742T>G
ENST00000680166.1:n.4447T>G
ENST00000680315.1:n.1041T>G
ENST00000680517.1:c.*546T>G	ENSP00000505803.1:n.*546T>G
ENST00000680582.1:n.2120T>G
ENST00000680613.1:c.*651T>G	ENSP00000506114.1:n.*651T>G
ENST00000680662.1:c.*1072T>G	ENSP00000505080.1:n.*1072T>G
ENST00000680691.1:c.*821T>G	ENSP00000506487.1:n.*821T>G
ENST00000680694.1:c.*746T>G	ENSP00000505658.1:n.*746T>G
ENST00000680743.1:c.*947T>G	ENSP00000505073.1:n.*947T>G
ENST00000680749.1:c.*443T>G	ENSP00000505122.1:n.*443T>G
ENST00000680798.1:c.*633T>G	ENSP00000505670.1:n.*633T>G
ENST00000680805.1:c.1017T>G	ENSP00000505447.1:p.Pro339=
ENST00000680844.1:c.*942T>G	ENSP00000506541.1:n.*942T>G
ENST00000680948.1:c.*1025T>G	ENSP00000505441.1:n.*1025T>G
ENST00000680964.1:c.*251T>G	ENSP00000505961.1:n.*251T>G
ENST00000681037.1:c.*2642T>G	ENSP00000506025.1:n.*2642T>G
ENST00000681063.1:c.*427T>G	ENSP00000506616.1:n.*427T>G
ENST00000681209.1:c.*813T>G	ENSP00000505877.1:n.*813T>G
ENST00000681278.1:n.1860T>G
ENST00000681289.1:n.5153T>G
ENST00000681361.1:c.*825T>G	ENSP00000506679.1:n.*825T>G
ENST00000681430.1:c.*251T>G	ENSP00000506301.1:n.*251T>G
ENST00000681446.1:c.*862T>G	ENSP00000506244.1:n.*862T>G
ENST00000681450.1:c.*829T>G	ENSP00000505660.1:n.*829T>G
ENST00000681548.1:c.*744T>G	ENSP00000505275.1:n.*744T>G
ENST00000681616.1:c.*817T>G	ENSP00000505111.1:n.*817T>G
ENST00000681621.1:c.*742T>G	ENSP00000505770.1:n.*742T>G
ENST00000681680.1:n.3253T>G
ENST00000681720.1:c.*613T>G	ENSP00000505438.1:n.*613T>G
ENST00000681730.1:n.1380T>G
ENST00000681790.1:c.900T>G	ENSP00000505130.1:p.Pro300=
ENST00000681837.1:n.1774T>G
ENST00000681913.1:n.3404T>G
ENST00000681916.1:c.*926T>G	ENSP00000506477.1:n.*926T>G
ENST00000681930.1:n.3282T>G
ENST00000370834.9:c.1257T>G	ENSP00000359871.5:p.Pro419=
ENST00000370841.8:c.1158T>G	ENSP00000359878.4:p.Pro386=
ENST00000420607.6:c.1170T>G	ENSP00000409612.2:p.Pro390=
ENST00000481374.1:n.431T>G
ENST00000525808.5:c.*744T>G	ENSP00000434823.1:n.*744T>G
ENST00000526129.5:c.*942T>G	ENSP00000434092.1:n.*942T>G
ENST00000526196.5:c.*926T>G	ENSP00000431953.1:n.*926T>G
ENST00000528016.1:c.160-7843T>G	ENSP00000434284.1:n.160-7843T>G
ENST00000529059.5:n.1067T>G
ENST00000541113.5:c.1050T>G	ENSP00000442324.1:p.Pro350=
NM_000016.5:c.1158T>G	NP_000007.1:p.Pro386=
NM_001127328.2:c.1170T>G	NP_001120800.1:p.Pro390=
NM_001286042.1:c.1050T>G	NP_001272971.1:p.Pro350=
NM_001286043.1:c.1257T>G	NP_001272972.1:p.Pro419=
NM_001286044.1:c.591T>G	NP_001272973.1:p.Pro197=
NM_000016.6:c.1158T>G MANE Select	NP_000007.1:p.Pro386=
NM_001127328.3:c.1170T>G	NP_001120800.1:p.Pro390=
NM_001286042.2:c.1050T>G	NP_001272971.1:p.Pro350=
NM_001286043.2:c.1257T>G	NP_001272972.1:p.Pro419=
NM_001286044.2:c.591T>G	NP_001272973.1:p.Pro197=