Canonical Allele Identifier: CA340817963

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226865T>A (hg19) ; chr1:g.75761180T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761180T>A , CM000663.2:g.75761180T>A	GRCh38
NC_000001.10:g.76226865T>A , CM000663.1:g.76226865T>A	GRCh37
NC_000001.9:g.75999453T>A	NCBI36
NG_007045.2:g.41823T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.1004T>A MANE Select	ENSP00000359878.5:p.Met335Lys
ENST00000473018.3:n.3128T>A
ENST00000532207.6:n.2015T>A
ENST00000541113.6:c.908T>A	ENSP00000442324.2:p.Met303Lys
ENST00000679509.1:n.1966T>A
ENST00000679530.1:c.*772T>A	ENSP00000506454.1:n.*772T>A
ENST00000679615.1:n.3019T>A
ENST00000679687.1:c.566T>A	ENSP00000506598.1:p.Met189Lys
ENST00000679704.1:c.*770T>A	ENSP00000505117.1:n.*770T>A
ENST00000679709.1:c.*967T>A	ENSP00000506623.1:n.*967T>A
ENST00000679976.1:c.*588T>A	ENSP00000505565.1:n.*588T>A
ENST00000680166.1:n.4293T>A
ENST00000680315.1:n.887T>A
ENST00000680517.1:c.*392T>A	ENSP00000505803.1:n.*392T>A
ENST00000680582.1:n.1966T>A
ENST00000680613.1:c.*497T>A	ENSP00000506114.1:n.*497T>A
ENST00000680662.1:c.*918T>A	ENSP00000505080.1:n.*918T>A
ENST00000680691.1:c.*667T>A	ENSP00000506487.1:n.*667T>A
ENST00000680694.1:c.*592T>A	ENSP00000505658.1:n.*592T>A
ENST00000680743.1:c.*793T>A	ENSP00000505073.1:n.*793T>A
ENST00000680749.1:c.*289T>A	ENSP00000505122.1:n.*289T>A
ENST00000680798.1:c.*479T>A	ENSP00000505670.1:n.*479T>A
ENST00000680805.1:c.863T>A	ENSP00000505447.1:p.Met288Lys
ENST00000680844.1:c.*788T>A	ENSP00000506541.1:n.*788T>A
ENST00000680948.1:c.*871T>A	ENSP00000505441.1:n.*871T>A
ENST00000680964.1:c.*97T>A	ENSP00000505961.1:n.*97T>A
ENST00000681037.1:c.*2488T>A	ENSP00000506025.1:n.*2488T>A
ENST00000681063.1:c.*273T>A	ENSP00000506616.1:n.*273T>A
ENST00000681209.1:c.*659T>A	ENSP00000505877.1:n.*659T>A
ENST00000681278.1:n.1706T>A
ENST00000681289.1:n.4999T>A
ENST00000681361.1:c.*671T>A	ENSP00000506679.1:n.*671T>A
ENST00000681430.1:c.*97T>A	ENSP00000506301.1:n.*97T>A
ENST00000681446.1:c.*708T>A	ENSP00000506244.1:n.*708T>A
ENST00000681450.1:c.*675T>A	ENSP00000505660.1:n.*675T>A
ENST00000681548.1:c.*590T>A	ENSP00000505275.1:n.*590T>A
ENST00000681616.1:c.*663T>A	ENSP00000505111.1:n.*663T>A
ENST00000681621.1:c.*588T>A	ENSP00000505770.1:n.*588T>A
ENST00000681680.1:n.3099T>A
ENST00000681720.1:c.*459T>A	ENSP00000505438.1:n.*459T>A
ENST00000681730.1:n.1226T>A
ENST00000681790.1:c.746T>A	ENSP00000505130.1:p.Met249Lys
ENST00000681837.1:n.1620T>A
ENST00000681913.1:n.3250T>A
ENST00000681916.1:c.*772T>A	ENSP00000506477.1:n.*772T>A
ENST00000681930.1:n.3128T>A
ENST00000370834.9:c.1103T>A	ENSP00000359871.5:p.Met368Lys
ENST00000370841.8:c.1004T>A	ENSP00000359878.4:p.Met335Lys
ENST00000420607.6:c.1016T>A	ENSP00000409612.2:p.Met339Lys
ENST00000481374.1:n.277T>A
ENST00000525808.5:c.*590T>A	ENSP00000434823.1:n.*590T>A
ENST00000526129.5:c.*788T>A	ENSP00000434092.1:n.*788T>A
ENST00000526196.5:c.*772T>A	ENSP00000431953.1:n.*772T>A
ENST00000528016.1:c.160-7997T>A	ENSP00000434284.1:n.160-7997T>A
ENST00000529059.5:n.913T>A
ENST00000532207.5:n.734T>A
ENST00000534334.5:c.*745T>A	ENSP00000435584.1:n.*745T>A
ENST00000541113.5:c.896T>A	ENSP00000442324.1:p.Met299Lys
NM_000016.5:c.1004T>A	NP_000007.1:p.Met335Lys
NM_001127328.2:c.1016T>A	NP_001120800.1:p.Met339Lys
NM_001286042.1:c.896T>A	NP_001272971.1:p.Met299Lys
NM_001286043.1:c.1103T>A	NP_001272972.1:p.Met368Lys
NM_001286044.1:c.437T>A	NP_001272973.1:p.Met146Lys
NM_000016.6:c.1004T>A MANE Select	NP_000007.1:p.Met335Lys
NM_001127328.3:c.1016T>A	NP_001120800.1:p.Met339Lys
NM_001286042.2:c.896T>A	NP_001272971.1:p.Met299Lys
NM_001286043.2:c.1103T>A	NP_001272972.1:p.Met368Lys
NM_001286044.2:c.437T>A	NP_001272973.1:p.Met146Lys