Canonical Allele Identifier: CA340818066

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226912A>T (hg19) ; chr1:g.75761227A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761227A>T , CM000663.2:g.75761227A>T	GRCh38
NC_000001.10:g.76226912A>T , CM000663.1:g.76226912A>T	GRCh37
NC_000001.9:g.75999500A>T	NCBI36
NG_007045.2:g.41870A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.1051A>T MANE Select	ENSP00000359878.5:p.Thr351Ser
ENST00000473018.3:n.3175A>T
ENST00000532207.6:n.2062A>T
ENST00000541113.6:c.955A>T	ENSP00000442324.2:p.Thr319Ser
ENST00000679509.1:n.2013A>T
ENST00000679530.1:c.*819A>T	ENSP00000506454.1:n.*819A>T
ENST00000679615.1:n.3066A>T
ENST00000679687.1:c.613A>T	ENSP00000506598.1:p.Thr205Ser
ENST00000679704.1:c.*817A>T	ENSP00000505117.1:n.*817A>T
ENST00000679709.1:c.*1014A>T	ENSP00000506623.1:n.*1014A>T
ENST00000679976.1:c.*635A>T	ENSP00000505565.1:n.*635A>T
ENST00000680166.1:n.4340A>T
ENST00000680315.1:n.934A>T
ENST00000680517.1:c.*439A>T	ENSP00000505803.1:n.*439A>T
ENST00000680582.1:n.2013A>T
ENST00000680613.1:c.*544A>T	ENSP00000506114.1:n.*544A>T
ENST00000680662.1:c.*965A>T	ENSP00000505080.1:n.*965A>T
ENST00000680691.1:c.*714A>T	ENSP00000506487.1:n.*714A>T
ENST00000680694.1:c.*639A>T	ENSP00000505658.1:n.*639A>T
ENST00000680743.1:c.*840A>T	ENSP00000505073.1:n.*840A>T
ENST00000680749.1:c.*336A>T	ENSP00000505122.1:n.*336A>T
ENST00000680798.1:c.*526A>T	ENSP00000505670.1:n.*526A>T
ENST00000680805.1:c.910A>T	ENSP00000505447.1:p.Thr304Ser
ENST00000680844.1:c.*835A>T	ENSP00000506541.1:n.*835A>T
ENST00000680948.1:c.*918A>T	ENSP00000505441.1:n.*918A>T
ENST00000680964.1:c.*144A>T	ENSP00000505961.1:n.*144A>T
ENST00000681037.1:c.*2535A>T	ENSP00000506025.1:n.*2535A>T
ENST00000681063.1:c.*320A>T	ENSP00000506616.1:n.*320A>T
ENST00000681209.1:c.*706A>T	ENSP00000505877.1:n.*706A>T
ENST00000681278.1:n.1753A>T
ENST00000681289.1:n.5046A>T
ENST00000681361.1:c.*718A>T	ENSP00000506679.1:n.*718A>T
ENST00000681430.1:c.*144A>T	ENSP00000506301.1:n.*144A>T
ENST00000681446.1:c.*755A>T	ENSP00000506244.1:n.*755A>T
ENST00000681450.1:c.*722A>T	ENSP00000505660.1:n.*722A>T
ENST00000681548.1:c.*637A>T	ENSP00000505275.1:n.*637A>T
ENST00000681616.1:c.*710A>T	ENSP00000505111.1:n.*710A>T
ENST00000681621.1:c.*635A>T	ENSP00000505770.1:n.*635A>T
ENST00000681680.1:n.3146A>T
ENST00000681720.1:c.*506A>T	ENSP00000505438.1:n.*506A>T
ENST00000681730.1:n.1273A>T
ENST00000681790.1:c.793A>T	ENSP00000505130.1:p.Thr265Ser
ENST00000681837.1:n.1667A>T
ENST00000681913.1:n.3297A>T
ENST00000681916.1:c.*819A>T	ENSP00000506477.1:n.*819A>T
ENST00000681930.1:n.3175A>T
ENST00000370834.9:c.1150A>T	ENSP00000359871.5:p.Thr384Ser
ENST00000370841.8:c.1051A>T	ENSP00000359878.4:p.Thr351Ser
ENST00000420607.6:c.1063A>T	ENSP00000409612.2:p.Thr355Ser
ENST00000481374.1:n.324A>T
ENST00000525808.5:c.*637A>T	ENSP00000434823.1:n.*637A>T
ENST00000526129.5:c.*835A>T	ENSP00000434092.1:n.*835A>T
ENST00000526196.5:c.*819A>T	ENSP00000431953.1:n.*819A>T
ENST00000528016.1:c.160-7950A>T	ENSP00000434284.1:n.160-7950A>T
ENST00000529059.5:n.960A>T
ENST00000534334.5:c.*792A>T	ENSP00000435584.1:n.*792A>T
ENST00000541113.5:c.943A>T	ENSP00000442324.1:p.Thr315Ser
NM_000016.5:c.1051A>T	NP_000007.1:p.Thr351Ser
NM_001127328.2:c.1063A>T	NP_001120800.1:p.Thr355Ser
NM_001286042.1:c.943A>T	NP_001272971.1:p.Thr315Ser
NM_001286043.1:c.1150A>T	NP_001272972.1:p.Thr384Ser
NM_001286044.1:c.484A>T	NP_001272973.1:p.Thr162Ser
NM_000016.6:c.1051A>T MANE Select	NP_000007.1:p.Thr351Ser
NM_001127328.3:c.1063A>T	NP_001120800.1:p.Thr355Ser
NM_001286042.2:c.943A>T	NP_001272971.1:p.Thr315Ser
NM_001286043.2:c.1150A>T	NP_001272972.1:p.Thr384Ser
NM_001286044.2:c.484A>T	NP_001272973.1:p.Thr162Ser