Canonical Allele Identifier: CA418707703

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226968T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761283T>A , CM000663.2:g.75761283T>A	GRCh38
NC_000001.10:g.76226968T>A , CM000663.1:g.76226968T>A	GRCh37
NC_000001.9:g.75999556T>A	NCBI36
NG_007045.2:g.41926T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.1107T>A MANE Select	ENSP00000359878.5:p.Ala369=
ENST00000473018.3:n.3231T>A
ENST00000532207.6:n.2118T>A
ENST00000541113.6:c.1011T>A	ENSP00000442324.2:p.Ala337=
ENST00000679509.1:n.2069T>A
ENST00000679530.1:c.*875T>A	ENSP00000506454.1:n.*875T>A
ENST00000679615.1:n.3122T>A
ENST00000679687.1:c.669T>A	ENSP00000506598.1:p.Ala223=
ENST00000679704.1:c.*873T>A	ENSP00000505117.1:n.*873T>A
ENST00000679709.1:c.*1070T>A	ENSP00000506623.1:n.*1070T>A
ENST00000679976.1:c.*691T>A	ENSP00000505565.1:n.*691T>A
ENST00000680166.1:n.4396T>A
ENST00000680315.1:n.990T>A
ENST00000680517.1:c.*495T>A	ENSP00000505803.1:n.*495T>A
ENST00000680582.1:n.2069T>A
ENST00000680613.1:c.*600T>A	ENSP00000506114.1:n.*600T>A
ENST00000680662.1:c.*1021T>A	ENSP00000505080.1:n.*1021T>A
ENST00000680691.1:c.*770T>A	ENSP00000506487.1:n.*770T>A
ENST00000680694.1:c.*695T>A	ENSP00000505658.1:n.*695T>A
ENST00000680743.1:c.*896T>A	ENSP00000505073.1:n.*896T>A
ENST00000680749.1:c.*392T>A	ENSP00000505122.1:n.*392T>A
ENST00000680798.1:c.*582T>A	ENSP00000505670.1:n.*582T>A
ENST00000680805.1:c.966T>A	ENSP00000505447.1:p.Ala322=
ENST00000680844.1:c.*891T>A	ENSP00000506541.1:n.*891T>A
ENST00000680948.1:c.*974T>A	ENSP00000505441.1:n.*974T>A
ENST00000680964.1:c.*200T>A	ENSP00000505961.1:n.*200T>A
ENST00000681037.1:c.*2591T>A	ENSP00000506025.1:n.*2591T>A
ENST00000681063.1:c.*376T>A	ENSP00000506616.1:n.*376T>A
ENST00000681209.1:c.*762T>A	ENSP00000505877.1:n.*762T>A
ENST00000681278.1:n.1809T>A
ENST00000681289.1:n.5102T>A
ENST00000681361.1:c.*774T>A	ENSP00000506679.1:n.*774T>A
ENST00000681430.1:c.*200T>A	ENSP00000506301.1:n.*200T>A
ENST00000681446.1:c.*811T>A	ENSP00000506244.1:n.*811T>A
ENST00000681450.1:c.*778T>A	ENSP00000505660.1:n.*778T>A
ENST00000681548.1:c.*693T>A	ENSP00000505275.1:n.*693T>A
ENST00000681616.1:c.*766T>A	ENSP00000505111.1:n.*766T>A
ENST00000681621.1:c.*691T>A	ENSP00000505770.1:n.*691T>A
ENST00000681680.1:n.3202T>A
ENST00000681720.1:c.*562T>A	ENSP00000505438.1:n.*562T>A
ENST00000681730.1:n.1329T>A
ENST00000681790.1:c.849T>A	ENSP00000505130.1:p.Ala283=
ENST00000681837.1:n.1723T>A
ENST00000681913.1:n.3353T>A
ENST00000681916.1:c.*875T>A	ENSP00000506477.1:n.*875T>A
ENST00000681930.1:n.3231T>A
ENST00000370834.9:c.1206T>A	ENSP00000359871.5:p.Ala402=
ENST00000370841.8:c.1107T>A	ENSP00000359878.4:p.Ala369=
ENST00000420607.6:c.1119T>A	ENSP00000409612.2:p.Ala373=
ENST00000481374.1:n.380T>A
ENST00000525808.5:c.*693T>A	ENSP00000434823.1:n.*693T>A
ENST00000526129.5:c.*891T>A	ENSP00000434092.1:n.*891T>A
ENST00000526196.5:c.*875T>A	ENSP00000431953.1:n.*875T>A
ENST00000528016.1:c.160-7894T>A	ENSP00000434284.1:n.160-7894T>A
ENST00000529059.5:n.1016T>A
ENST00000541113.5:c.999T>A	ENSP00000442324.1:p.Ala333=
NM_000016.5:c.1107T>A	NP_000007.1:p.Ala369=
NM_001127328.2:c.1119T>A	NP_001120800.1:p.Ala373=
NM_001286042.1:c.999T>A	NP_001272971.1:p.Ala333=
NM_001286043.1:c.1206T>A	NP_001272972.1:p.Ala402=
NM_001286044.1:c.540T>A	NP_001272973.1:p.Ala180=
NM_000016.6:c.1107T>A MANE Select	NP_000007.1:p.Ala369=
NM_001127328.3:c.1119T>A	NP_001120800.1:p.Ala373=
NM_001286042.2:c.999T>A	NP_001272971.1:p.Ala333=
NM_001286043.2:c.1206T>A	NP_001272972.1:p.Ala402=
NM_001286044.2:c.540T>A	NP_001272973.1:p.Ala180=