Canonical Allele Identifier: CA340816826

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76215236A>T (hg19) ; chr1:g.75749551A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75749551A>T , CM000663.2:g.75749551A>T	GRCh38
NC_000001.10:g.76215236A>T , CM000663.1:g.76215236A>T	GRCh37
NC_000001.9:g.75987824A>T	NCBI36
NG_007045.2:g.30194A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.841A>T MANE Select	ENSP00000359878.5:p.Arg281Ter
ENST00000473018.3:n.2965A>T
ENST00000532207.6:n.1730A>T
ENST00000541113.6:c.841A>T	ENSP00000442324.2:p.Arg281Ter
ENST00000679509.1:n.1803A>T
ENST00000679530.1:c.*609A>T	ENSP00000506454.1:n.*609A>T
ENST00000679615.1:n.2856A>T
ENST00000679687.1:c.403A>T	ENSP00000506598.1:p.Arg135Ter
ENST00000679704.1:c.*607A>T	ENSP00000505117.1:n.*607A>T
ENST00000679709.1:c.*804A>T	ENSP00000506623.1:n.*804A>T
ENST00000679976.1:c.*425A>T	ENSP00000505565.1:n.*425A>T
ENST00000680166.1:n.4130A>T
ENST00000680517.1:c.*229A>T	ENSP00000505803.1:n.*229A>T
ENST00000680582.1:n.1803A>T
ENST00000680613.1:c.*212A>T	ENSP00000506114.1:n.*212A>T
ENST00000680662.1:c.*755A>T	ENSP00000505080.1:n.*755A>T
ENST00000680691.1:c.*504A>T	ENSP00000506487.1:n.*504A>T
ENST00000680694.1:c.*429A>T	ENSP00000505658.1:n.*429A>T
ENST00000680743.1:c.*508A>T	ENSP00000505073.1:n.*508A>T
ENST00000680749.1:c.*126A>T	ENSP00000505122.1:n.*126A>T
ENST00000680798.1:c.*316A>T	ENSP00000505670.1:n.*316A>T
ENST00000680805.1:c.709-900A>T	ENSP00000505447.1:n.709-900A>T
ENST00000680844.1:c.*625A>T	ENSP00000506541.1:n.*625A>T
ENST00000680948.1:c.*708A>T	ENSP00000505441.1:n.*708A>T
ENST00000680964.1:c.841A>T	ENSP00000505961.1:p.Arg281Ter
ENST00000681037.1:c.*2325A>T	ENSP00000506025.1:n.*2325A>T
ENST00000681063.1:c.600-900A>T	ENSP00000506616.1:n.600-900A>T
ENST00000681209.1:c.*496A>T	ENSP00000505877.1:n.*496A>T
ENST00000681278.1:n.1198A>T
ENST00000681289.1:n.4836A>T
ENST00000681361.1:c.*508A>T	ENSP00000506679.1:n.*508A>T
ENST00000681430.1:c.841A>T	ENSP00000506301.1:p.Arg281Ter
ENST00000681446.1:c.*423A>T	ENSP00000506244.1:n.*423A>T
ENST00000681450.1:c.*512A>T	ENSP00000505660.1:n.*512A>T
ENST00000681548.1:c.*427A>T	ENSP00000505275.1:n.*427A>T
ENST00000681616.1:c.*500A>T	ENSP00000505111.1:n.*500A>T
ENST00000681621.1:c.*425A>T	ENSP00000505770.1:n.*425A>T
ENST00000681680.1:n.2936A>T
ENST00000681720.1:c.*296A>T	ENSP00000505438.1:n.*296A>T
ENST00000681730.1:n.1063A>T
ENST00000681790.1:c.583A>T	ENSP00000505130.1:p.Arg195Ter
ENST00000681837.1:n.1457A>T
ENST00000681913.1:n.2965A>T
ENST00000681916.1:c.*609A>T	ENSP00000506477.1:n.*609A>T
ENST00000681930.1:n.2965A>T
ENST00000370834.9:c.940A>T	ENSP00000359871.5:p.Arg314Ter
ENST00000370841.8:c.841A>T	ENSP00000359878.4:p.Arg281Ter
ENST00000420607.6:c.853A>T	ENSP00000409612.2:p.Arg285Ter
ENST00000525808.5:c.*427A>T	ENSP00000434823.1:n.*427A>T
ENST00000526129.5:c.*625A>T	ENSP00000434092.1:n.*625A>T
ENST00000526196.5:c.*609A>T	ENSP00000431953.1:n.*609A>T
ENST00000528016.1:c.55A>T	ENSP00000434284.1:p.Arg19Ter
ENST00000529059.5:n.750A>T
ENST00000532207.5:n.571A>T
ENST00000532509.5:c.*605A>T	ENSP00000432522.1:n.*605A>T
ENST00000534334.5:c.*425A>T	ENSP00000435584.1:n.*425A>T
ENST00000541113.5:c.733A>T	ENSP00000442324.1:p.Arg245Ter
NM_000016.5:c.841A>T	NP_000007.1:p.Arg281Ter
NM_001127328.2:c.853A>T	NP_001120800.1:p.Arg285Ter
NM_001286042.1:c.733A>T	NP_001272971.1:p.Arg245Ter
NM_001286043.1:c.940A>T	NP_001272972.1:p.Arg314Ter
NM_001286044.1:c.274A>T	NP_001272973.1:p.Arg92Ter
NM_000016.6:c.841A>T MANE Select	NP_000007.1:p.Arg281Ter
NM_001127328.3:c.853A>T	NP_001120800.1:p.Arg285Ter
NM_001286042.2:c.733A>T	NP_001272971.1:p.Arg245Ter
NM_001286043.2:c.940A>T	NP_001272972.1:p.Arg314Ter
NM_001286044.2:c.274A>T	NP_001272973.1:p.Arg92Ter