Canonical Allele Identifier: CA418707650

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226935G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761250G>A , CM000663.2:g.75761250G>A	GRCh38
NC_000001.10:g.76226935G>A , CM000663.1:g.76226935G>A	GRCh37
NC_000001.9:g.75999523G>A	NCBI36
NG_007045.2:g.41893G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.1074G>A MANE Select	ENSP00000359878.5:p.Lys358=
ENST00000473018.3:n.3198G>A
ENST00000532207.6:n.2085G>A
ENST00000541113.6:c.978G>A	ENSP00000442324.2:p.Lys326=
ENST00000679509.1:n.2036G>A
ENST00000679530.1:c.*842G>A	ENSP00000506454.1:n.*842G>A
ENST00000679615.1:n.3089G>A
ENST00000679687.1:c.636G>A	ENSP00000506598.1:p.Lys212=
ENST00000679704.1:c.*840G>A	ENSP00000505117.1:n.*840G>A
ENST00000679709.1:c.*1037G>A	ENSP00000506623.1:n.*1037G>A
ENST00000679976.1:c.*658G>A	ENSP00000505565.1:n.*658G>A
ENST00000680166.1:n.4363G>A
ENST00000680315.1:n.957G>A
ENST00000680517.1:c.*462G>A	ENSP00000505803.1:n.*462G>A
ENST00000680582.1:n.2036G>A
ENST00000680613.1:c.*567G>A	ENSP00000506114.1:n.*567G>A
ENST00000680662.1:c.*988G>A	ENSP00000505080.1:n.*988G>A
ENST00000680691.1:c.*737G>A	ENSP00000506487.1:n.*737G>A
ENST00000680694.1:c.*662G>A	ENSP00000505658.1:n.*662G>A
ENST00000680743.1:c.*863G>A	ENSP00000505073.1:n.*863G>A
ENST00000680749.1:c.*359G>A	ENSP00000505122.1:n.*359G>A
ENST00000680798.1:c.*549G>A	ENSP00000505670.1:n.*549G>A
ENST00000680805.1:c.933G>A	ENSP00000505447.1:p.Lys311=
ENST00000680844.1:c.*858G>A	ENSP00000506541.1:n.*858G>A
ENST00000680948.1:c.*941G>A	ENSP00000505441.1:n.*941G>A
ENST00000680964.1:c.*167G>A	ENSP00000505961.1:n.*167G>A
ENST00000681037.1:c.*2558G>A	ENSP00000506025.1:n.*2558G>A
ENST00000681063.1:c.*343G>A	ENSP00000506616.1:n.*343G>A
ENST00000681209.1:c.*729G>A	ENSP00000505877.1:n.*729G>A
ENST00000681278.1:n.1776G>A
ENST00000681289.1:n.5069G>A
ENST00000681361.1:c.*741G>A	ENSP00000506679.1:n.*741G>A
ENST00000681430.1:c.*167G>A	ENSP00000506301.1:n.*167G>A
ENST00000681446.1:c.*778G>A	ENSP00000506244.1:n.*778G>A
ENST00000681450.1:c.*745G>A	ENSP00000505660.1:n.*745G>A
ENST00000681548.1:c.*660G>A	ENSP00000505275.1:n.*660G>A
ENST00000681616.1:c.*733G>A	ENSP00000505111.1:n.*733G>A
ENST00000681621.1:c.*658G>A	ENSP00000505770.1:n.*658G>A
ENST00000681680.1:n.3169G>A
ENST00000681720.1:c.*529G>A	ENSP00000505438.1:n.*529G>A
ENST00000681730.1:n.1296G>A
ENST00000681790.1:c.816G>A	ENSP00000505130.1:p.Lys272=
ENST00000681837.1:n.1690G>A
ENST00000681913.1:n.3320G>A
ENST00000681916.1:c.*842G>A	ENSP00000506477.1:n.*842G>A
ENST00000681930.1:n.3198G>A
ENST00000370834.9:c.1173G>A	ENSP00000359871.5:p.Lys391=
ENST00000370841.8:c.1074G>A	ENSP00000359878.4:p.Lys358=
ENST00000420607.6:c.1086G>A	ENSP00000409612.2:p.Lys362=
ENST00000481374.1:n.347G>A
ENST00000525808.5:c.*660G>A	ENSP00000434823.1:n.*660G>A
ENST00000526129.5:c.*858G>A	ENSP00000434092.1:n.*858G>A
ENST00000526196.5:c.*842G>A	ENSP00000431953.1:n.*842G>A
ENST00000528016.1:c.160-7927G>A	ENSP00000434284.1:n.160-7927G>A
ENST00000529059.5:n.983G>A
ENST00000541113.5:c.966G>A	ENSP00000442324.1:p.Lys322=
NM_000016.5:c.1074G>A	NP_000007.1:p.Lys358=
NM_001127328.2:c.1086G>A	NP_001120800.1:p.Lys362=
NM_001286042.1:c.966G>A	NP_001272971.1:p.Lys322=
NM_001286043.1:c.1173G>A	NP_001272972.1:p.Lys391=
NM_001286044.1:c.507G>A	NP_001272973.1:p.Lys169=
NM_000016.6:c.1074G>A MANE Select	NP_000007.1:p.Lys358=
NM_001127328.3:c.1086G>A	NP_001120800.1:p.Lys362=
NM_001286042.2:c.966G>A	NP_001272971.1:p.Lys322=
NM_001286043.2:c.1173G>A	NP_001272972.1:p.Lys391=
NM_001286044.2:c.507G>A	NP_001272973.1:p.Lys169=