Canonical Allele Identifier: CA418544889

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76215196A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75749511A>C , CM000663.2:g.75749511A>C	GRCh38
NC_000001.10:g.76215196A>C , CM000663.1:g.76215196A>C	GRCh37
NC_000001.9:g.75987784A>C	NCBI36
NG_007045.2:g.30154A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.801A>C MANE Select	ENSP00000359878.5:p.Gly267=
ENST00000473018.3:n.2925A>C
ENST00000532207.6:n.1690A>C
ENST00000541113.6:c.801A>C	ENSP00000442324.2:p.Gly267=
ENST00000679509.1:n.1763A>C
ENST00000679530.1:c.*569A>C	ENSP00000506454.1:n.*569A>C
ENST00000679615.1:n.2816A>C
ENST00000679687.1:c.363A>C	ENSP00000506598.1:p.Gly121=
ENST00000679704.1:c.*567A>C	ENSP00000505117.1:n.*567A>C
ENST00000679709.1:c.*764A>C	ENSP00000506623.1:n.*764A>C
ENST00000679976.1:c.*385A>C	ENSP00000505565.1:n.*385A>C
ENST00000680166.1:n.4090A>C
ENST00000680517.1:c.*189A>C	ENSP00000505803.1:n.*189A>C
ENST00000680582.1:n.1763A>C
ENST00000680613.1:c.*172A>C	ENSP00000506114.1:n.*172A>C
ENST00000680662.1:c.*715A>C	ENSP00000505080.1:n.*715A>C
ENST00000680691.1:c.*464A>C	ENSP00000506487.1:n.*464A>C
ENST00000680694.1:c.*389A>C	ENSP00000505658.1:n.*389A>C
ENST00000680743.1:c.*468A>C	ENSP00000505073.1:n.*468A>C
ENST00000680749.1:c.*86A>C	ENSP00000505122.1:n.*86A>C
ENST00000680798.1:c.*276A>C	ENSP00000505670.1:n.*276A>C
ENST00000680805.1:c.709-940A>C	ENSP00000505447.1:n.709-940A>C
ENST00000680844.1:c.*585A>C	ENSP00000506541.1:n.*585A>C
ENST00000680948.1:c.*668A>C	ENSP00000505441.1:n.*668A>C
ENST00000680964.1:c.801A>C	ENSP00000505961.1:p.Gly267=
ENST00000681037.1:c.*2285A>C	ENSP00000506025.1:n.*2285A>C
ENST00000681063.1:c.600-940A>C	ENSP00000506616.1:n.600-940A>C
ENST00000681209.1:c.*456A>C	ENSP00000505877.1:n.*456A>C
ENST00000681278.1:n.1158A>C
ENST00000681289.1:n.4796A>C
ENST00000681361.1:c.*468A>C	ENSP00000506679.1:n.*468A>C
ENST00000681430.1:c.801A>C	ENSP00000506301.1:p.Gly267=
ENST00000681446.1:c.*383A>C	ENSP00000506244.1:n.*383A>C
ENST00000681450.1:c.*472A>C	ENSP00000505660.1:n.*472A>C
ENST00000681548.1:c.*387A>C	ENSP00000505275.1:n.*387A>C
ENST00000681616.1:c.*460A>C	ENSP00000505111.1:n.*460A>C
ENST00000681621.1:c.*385A>C	ENSP00000505770.1:n.*385A>C
ENST00000681680.1:n.2896A>C
ENST00000681720.1:c.*256A>C	ENSP00000505438.1:n.*256A>C
ENST00000681730.1:n.1023A>C
ENST00000681790.1:c.543A>C	ENSP00000505130.1:p.Gly181=
ENST00000681837.1:n.1417A>C
ENST00000681913.1:n.2925A>C
ENST00000681916.1:c.*569A>C	ENSP00000506477.1:n.*569A>C
ENST00000681930.1:n.2925A>C
ENST00000370834.9:c.900A>C	ENSP00000359871.5:p.Gly300=
ENST00000370841.8:c.801A>C	ENSP00000359878.4:p.Gly267=
ENST00000420607.6:c.813A>C	ENSP00000409612.2:p.Gly271=
ENST00000525808.5:c.*387A>C	ENSP00000434823.1:n.*387A>C
ENST00000526129.5:c.*585A>C	ENSP00000434092.1:n.*585A>C
ENST00000526196.5:c.*569A>C	ENSP00000431953.1:n.*569A>C
ENST00000526930.1:n.574A>C
ENST00000528016.1:c.15A>C	ENSP00000434284.1:p.Gly5=
ENST00000529059.5:n.710A>C
ENST00000530953.6:c.*298A>C	ENSP00000431372.1:n.*298A>C
ENST00000532207.5:n.531A>C
ENST00000532509.5:c.*565A>C	ENSP00000432522.1:n.*565A>C
ENST00000534334.5:c.*385A>C	ENSP00000435584.1:n.*385A>C
ENST00000541113.5:c.693A>C	ENSP00000442324.1:p.Gly231=
NM_000016.5:c.801A>C	NP_000007.1:p.Gly267=
NM_001127328.2:c.813A>C	NP_001120800.1:p.Gly271=
NM_001286042.1:c.693A>C	NP_001272971.1:p.Gly231=
NM_001286043.1:c.900A>C	NP_001272972.1:p.Gly300=
NM_001286044.1:c.234A>C	NP_001272973.1:p.Gly78=
NM_000016.6:c.801A>C MANE Select	NP_000007.1:p.Gly267=
NM_001127328.3:c.813A>C	NP_001120800.1:p.Gly271=
NM_001286042.2:c.693A>C	NP_001272971.1:p.Gly231=
NM_001286043.2:c.900A>C	NP_001272972.1:p.Gly300=
NM_001286044.2:c.234A>C	NP_001272973.1:p.Gly78=