Canonical Allele Identifier: CA340817100

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76216191A>T (hg19) ; chr1:g.75750506A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75750506A>T , CM000663.2:g.75750506A>T	GRCh38
NC_000001.10:g.76216191A>T , CM000663.1:g.76216191A>T	GRCh37
NC_000001.9:g.75988779A>T	NCBI36
NG_007045.2:g.31149A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.905A>T MANE Select	ENSP00000359878.5:p.Tyr302Phe
ENST00000473018.3:n.3029A>T
ENST00000532207.6:n.1794A>T
ENST00000541113.6:c.849+947A>T	ENSP00000442324.2:n.849+947A>T
ENST00000679509.1:n.1867A>T
ENST00000679530.1:c.*673A>T	ENSP00000506454.1:n.*673A>T
ENST00000679615.1:n.2920A>T
ENST00000679687.1:c.467A>T	ENSP00000506598.1:p.Tyr156Phe
ENST00000679704.1:c.*671A>T	ENSP00000505117.1:n.*671A>T
ENST00000679709.1:c.*868A>T	ENSP00000506623.1:n.*868A>T
ENST00000679976.1:c.*489A>T	ENSP00000505565.1:n.*489A>T
ENST00000680166.1:n.4194A>T
ENST00000680315.1:n.788A>T
ENST00000680517.1:c.*293A>T	ENSP00000505803.1:n.*293A>T
ENST00000680582.1:n.1867A>T
ENST00000680613.1:c.*276A>T	ENSP00000506114.1:n.*276A>T
ENST00000680662.1:c.*819A>T	ENSP00000505080.1:n.*819A>T
ENST00000680691.1:c.*568A>T	ENSP00000506487.1:n.*568A>T
ENST00000680694.1:c.*493A>T	ENSP00000505658.1:n.*493A>T
ENST00000680743.1:c.*572A>T	ENSP00000505073.1:n.*572A>T
ENST00000680749.1:c.*190A>T	ENSP00000505122.1:n.*190A>T
ENST00000680798.1:c.*380A>T	ENSP00000505670.1:n.*380A>T
ENST00000680805.1:c.764A>T	ENSP00000505447.1:p.Tyr255Phe
ENST00000680844.1:c.*689A>T	ENSP00000506541.1:n.*689A>T
ENST00000680948.1:c.*772A>T	ENSP00000505441.1:n.*772A>T
ENST00000680964.1:c.905A>T	ENSP00000505961.1:p.Tyr302Phe
ENST00000681037.1:c.*2389A>T	ENSP00000506025.1:n.*2389A>T
ENST00000681063.1:c.*52A>T	ENSP00000506616.1:n.*52A>T
ENST00000681209.1:c.*560A>T	ENSP00000505877.1:n.*560A>T
ENST00000681278.1:n.1262A>T
ENST00000681289.1:n.4900A>T
ENST00000681361.1:c.*572A>T	ENSP00000506679.1:n.*572A>T
ENST00000681430.1:c.905A>T	ENSP00000506301.1:p.Tyr302Phe
ENST00000681446.1:c.*487A>T	ENSP00000506244.1:n.*487A>T
ENST00000681450.1:c.*576A>T	ENSP00000505660.1:n.*576A>T
ENST00000681548.1:c.*491A>T	ENSP00000505275.1:n.*491A>T
ENST00000681616.1:c.*564A>T	ENSP00000505111.1:n.*564A>T
ENST00000681621.1:c.*489A>T	ENSP00000505770.1:n.*489A>T
ENST00000681680.1:n.3000A>T
ENST00000681720.1:c.*360A>T	ENSP00000505438.1:n.*360A>T
ENST00000681730.1:n.1127A>T
ENST00000681790.1:c.647A>T	ENSP00000505130.1:p.Tyr216Phe
ENST00000681837.1:n.1521A>T
ENST00000681913.1:n.3029A>T
ENST00000681916.1:c.*673A>T	ENSP00000506477.1:n.*673A>T
ENST00000681930.1:n.3029A>T
ENST00000370834.9:c.1004A>T	ENSP00000359871.5:p.Tyr335Phe
ENST00000370841.8:c.905A>T	ENSP00000359878.4:p.Tyr302Phe
ENST00000420607.6:c.917A>T	ENSP00000409612.2:p.Tyr306Phe
ENST00000481374.1:n.56A>T
ENST00000525808.5:c.*491A>T	ENSP00000434823.1:n.*491A>T
ENST00000526129.5:c.*689A>T	ENSP00000434092.1:n.*689A>T
ENST00000526196.5:c.*673A>T	ENSP00000431953.1:n.*673A>T
ENST00000528016.1:c.119A>T	ENSP00000434284.1:p.Tyr40Phe
ENST00000529059.5:n.814A>T
ENST00000532207.5:n.635A>T
ENST00000534334.5:c.*489A>T	ENSP00000435584.1:n.*489A>T
ENST00000541113.5:c.797A>T	ENSP00000442324.1:p.Tyr266Phe
NM_000016.5:c.905A>T	NP_000007.1:p.Tyr302Phe
NM_001127328.2:c.917A>T	NP_001120800.1:p.Tyr306Phe
NM_001286042.1:c.797A>T	NP_001272971.1:p.Tyr266Phe
NM_001286043.1:c.1004A>T	NP_001272972.1:p.Tyr335Phe
NM_001286044.1:c.338A>T	NP_001272973.1:p.Tyr113Phe
NM_000016.6:c.905A>T MANE Select	NP_000007.1:p.Tyr302Phe
NM_001127328.3:c.917A>T	NP_001120800.1:p.Tyr306Phe
NM_001286042.2:c.797A>T	NP_001272971.1:p.Tyr266Phe
NM_001286043.2:c.1004A>T	NP_001272972.1:p.Tyr335Phe
NM_001286044.2:c.338A>T	NP_001272973.1:p.Tyr113Phe