Canonical Allele Identifier: CA418544921

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76215214A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75749529A>T , CM000663.2:g.75749529A>T	GRCh38
NC_000001.10:g.76215214A>T , CM000663.1:g.76215214A>T	GRCh37
NC_000001.9:g.75987802A>T	NCBI36
NG_007045.2:g.30172A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.819A>T MANE Select	ENSP00000359878.5:p.Ala273=
ENST00000473018.3:n.2943A>T
ENST00000532207.6:n.1708A>T
ENST00000541113.6:c.819A>T	ENSP00000442324.2:p.Ala273=
ENST00000679509.1:n.1781A>T
ENST00000679530.1:c.*587A>T	ENSP00000506454.1:n.*587A>T
ENST00000679615.1:n.2834A>T
ENST00000679687.1:c.381A>T	ENSP00000506598.1:p.Ala127=
ENST00000679704.1:c.*585A>T	ENSP00000505117.1:n.*585A>T
ENST00000679709.1:c.*782A>T	ENSP00000506623.1:n.*782A>T
ENST00000679976.1:c.*403A>T	ENSP00000505565.1:n.*403A>T
ENST00000680166.1:n.4108A>T
ENST00000680517.1:c.*207A>T	ENSP00000505803.1:n.*207A>T
ENST00000680582.1:n.1781A>T
ENST00000680613.1:c.*190A>T	ENSP00000506114.1:n.*190A>T
ENST00000680662.1:c.*733A>T	ENSP00000505080.1:n.*733A>T
ENST00000680691.1:c.*482A>T	ENSP00000506487.1:n.*482A>T
ENST00000680694.1:c.*407A>T	ENSP00000505658.1:n.*407A>T
ENST00000680743.1:c.*486A>T	ENSP00000505073.1:n.*486A>T
ENST00000680749.1:c.*104A>T	ENSP00000505122.1:n.*104A>T
ENST00000680798.1:c.*294A>T	ENSP00000505670.1:n.*294A>T
ENST00000680805.1:c.709-922A>T	ENSP00000505447.1:n.709-922A>T
ENST00000680844.1:c.*603A>T	ENSP00000506541.1:n.*603A>T
ENST00000680948.1:c.*686A>T	ENSP00000505441.1:n.*686A>T
ENST00000680964.1:c.819A>T	ENSP00000505961.1:p.Ala273=
ENST00000681037.1:c.*2303A>T	ENSP00000506025.1:n.*2303A>T
ENST00000681063.1:c.600-922A>T	ENSP00000506616.1:n.600-922A>T
ENST00000681209.1:c.*474A>T	ENSP00000505877.1:n.*474A>T
ENST00000681278.1:n.1176A>T
ENST00000681289.1:n.4814A>T
ENST00000681361.1:c.*486A>T	ENSP00000506679.1:n.*486A>T
ENST00000681430.1:c.819A>T	ENSP00000506301.1:p.Ala273=
ENST00000681446.1:c.*401A>T	ENSP00000506244.1:n.*401A>T
ENST00000681450.1:c.*490A>T	ENSP00000505660.1:n.*490A>T
ENST00000681548.1:c.*405A>T	ENSP00000505275.1:n.*405A>T
ENST00000681616.1:c.*478A>T	ENSP00000505111.1:n.*478A>T
ENST00000681621.1:c.*403A>T	ENSP00000505770.1:n.*403A>T
ENST00000681680.1:n.2914A>T
ENST00000681720.1:c.*274A>T	ENSP00000505438.1:n.*274A>T
ENST00000681730.1:n.1041A>T
ENST00000681790.1:c.561A>T	ENSP00000505130.1:p.Ala187=
ENST00000681837.1:n.1435A>T
ENST00000681913.1:n.2943A>T
ENST00000681916.1:c.*587A>T	ENSP00000506477.1:n.*587A>T
ENST00000681930.1:n.2943A>T
ENST00000370834.9:c.918A>T	ENSP00000359871.5:p.Ala306=
ENST00000370841.8:c.819A>T	ENSP00000359878.4:p.Ala273=
ENST00000420607.6:c.831A>T	ENSP00000409612.2:p.Ala277=
ENST00000525808.5:c.*405A>T	ENSP00000434823.1:n.*405A>T
ENST00000526129.5:c.*603A>T	ENSP00000434092.1:n.*603A>T
ENST00000526196.5:c.*587A>T	ENSP00000431953.1:n.*587A>T
ENST00000528016.1:c.33A>T	ENSP00000434284.1:p.Ala11=
ENST00000529059.5:n.728A>T
ENST00000530953.6:c.*316A>T	ENSP00000431372.1:n.*316A>T
ENST00000532207.5:n.549A>T
ENST00000532509.5:c.*583A>T	ENSP00000432522.1:n.*583A>T
ENST00000534334.5:c.*403A>T	ENSP00000435584.1:n.*403A>T
ENST00000541113.5:c.711A>T	ENSP00000442324.1:p.Ala237=
NM_000016.5:c.819A>T	NP_000007.1:p.Ala273=
NM_001127328.2:c.831A>T	NP_001120800.1:p.Ala277=
NM_001286042.1:c.711A>T	NP_001272971.1:p.Ala237=
NM_001286043.1:c.918A>T	NP_001272972.1:p.Ala306=
NM_001286044.1:c.252A>T	NP_001272973.1:p.Ala84=
NM_000016.6:c.819A>T MANE Select	NP_000007.1:p.Ala273=
NM_001127328.3:c.831A>T	NP_001120800.1:p.Ala277=
NM_001286042.2:c.711A>T	NP_001272971.1:p.Ala237=
NM_001286043.2:c.918A>T	NP_001272972.1:p.Ala306=
NM_001286044.2:c.252A>T	NP_001272973.1:p.Ala84=