Canonical Allele Identifier: CA418545018

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76216161_76216162insCTT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75750476_75750477insCTT , CM000663.2:g.75750476_75750477insCTT	GRCh38
NC_000001.10:g.76216161_76216162insCTT , CM000663.1:g.76216161_76216162insCTT	GRCh37
NC_000001.9:g.75988749_75988750insCTT	NCBI36
NG_007045.2:g.31119_31120insCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.875_876insCTT MANE Select	ENSP00000359878.5:p.Ala292_Gln293insLeu
ENST00000473018.3:n.2999_3000insCTT
ENST00000532207.6:n.1764_1765insCTT
ENST00000541113.6:c.849+917_849+918insCTT	ENSP00000442324.2:n.849+917_849+918insCTT
ENST00000679509.1:n.1837_1838insCTT
ENST00000679530.1:c.*643_*644insCTT	ENSP00000506454.1:n.*643_*644insCTT
ENST00000679615.1:n.2890_2891insCTT
ENST00000679687.1:c.437_438insCTT	ENSP00000506598.1:p.Ala146_Gln147insLeu
ENST00000679704.1:c.*641_*642insCTT	ENSP00000505117.1:n.*641_*642insCTT
ENST00000679709.1:c.*838_*839insCTT	ENSP00000506623.1:n.*838_*839insCTT
ENST00000679976.1:c.*459_*460insCTT	ENSP00000505565.1:n.*459_*460insCTT
ENST00000680166.1:n.4164_4165insCTT
ENST00000680315.1:n.758_759insCTT
ENST00000680517.1:c.*263_*264insCTT	ENSP00000505803.1:n.*263_*264insCTT
ENST00000680582.1:n.1837_1838insCTT
ENST00000680613.1:c.*246_*247insCTT	ENSP00000506114.1:n.*246_*247insCTT
ENST00000680662.1:c.*789_*790insCTT	ENSP00000505080.1:n.*789_*790insCTT
ENST00000680691.1:c.*538_*539insCTT	ENSP00000506487.1:n.*538_*539insCTT
ENST00000680694.1:c.*463_*464insCTT	ENSP00000505658.1:n.*463_*464insCTT
ENST00000680743.1:c.*542_*543insCTT	ENSP00000505073.1:n.*542_*543insCTT
ENST00000680749.1:c.*160_*161insCTT	ENSP00000505122.1:n.*160_*161insCTT
ENST00000680798.1:c.*350_*351insCTT	ENSP00000505670.1:n.*350_*351insCTT
ENST00000680805.1:c.734_735insCTT	ENSP00000505447.1:p.Ala245_Gln246insLeu
ENST00000680844.1:c.*659_*660insCTT	ENSP00000506541.1:n.*659_*660insCTT
ENST00000680948.1:c.*742_*743insCTT	ENSP00000505441.1:n.*742_*743insCTT
ENST00000680964.1:c.875_876insCTT	ENSP00000505961.1:p.Ala292_Gln293insLeu
ENST00000681037.1:c.*2359_*2360insCTT	ENSP00000506025.1:n.*2359_*2360insCTT
ENST00000681063.1:c.*22_*23insCTT	ENSP00000506616.1:n.*22_*23insCTT
ENST00000681209.1:c.*530_*531insCTT	ENSP00000505877.1:n.*530_*531insCTT
ENST00000681278.1:n.1232_1233insCTT
ENST00000681289.1:n.4870_4871insCTT
ENST00000681361.1:c.*542_*543insCTT	ENSP00000506679.1:n.*542_*543insCTT
ENST00000681430.1:c.875_876insCTT	ENSP00000506301.1:p.Ala292_Gln293insLeu
ENST00000681446.1:c.*457_*458insCTT	ENSP00000506244.1:n.*457_*458insCTT
ENST00000681450.1:c.*546_*547insCTT	ENSP00000505660.1:n.*546_*547insCTT
ENST00000681548.1:c.*461_*462insCTT	ENSP00000505275.1:n.*461_*462insCTT
ENST00000681616.1:c.*534_*535insCTT	ENSP00000505111.1:n.*534_*535insCTT
ENST00000681621.1:c.*459_*460insCTT	ENSP00000505770.1:n.*459_*460insCTT
ENST00000681680.1:n.2970_2971insCTT
ENST00000681720.1:c.*330_*331insCTT	ENSP00000505438.1:n.*330_*331insCTT
ENST00000681730.1:n.1097_1098insCTT
ENST00000681790.1:c.617_618insCTT	ENSP00000505130.1:p.Ala206_Gln207insLeu
ENST00000681837.1:n.1491_1492insCTT
ENST00000681913.1:n.2999_3000insCTT
ENST00000681916.1:c.*643_*644insCTT	ENSP00000506477.1:n.*643_*644insCTT
ENST00000681930.1:n.2999_3000insCTT
ENST00000370834.9:c.974_975insCTT	ENSP00000359871.5:p.Ala325_Gln326insLeu
ENST00000370841.8:c.875_876insCTT	ENSP00000359878.4:p.Ala292_Gln293insLeu
ENST00000420607.6:c.887_888insCTT	ENSP00000409612.2:p.Ala296_Gln297insLeu
ENST00000481374.1:n.26_27insCTT
ENST00000525808.5:c.*461_*462insCTT	ENSP00000434823.1:n.*461_*462insCTT
ENST00000526129.5:c.*659_*660insCTT	ENSP00000434092.1:n.*659_*660insCTT
ENST00000526196.5:c.*643_*644insCTT	ENSP00000431953.1:n.*643_*644insCTT
ENST00000528016.1:c.89_90insCTT	ENSP00000434284.1:p.Ala30_Gln31insLeu
ENST00000529059.5:n.784_785insCTT
ENST00000532207.5:n.605_606insCTT
ENST00000534334.5:c.*459_*460insCTT	ENSP00000435584.1:n.*459_*460insCTT
ENST00000541113.5:c.767_768insCTT	ENSP00000442324.1:p.Ala256_Gln257insLeu
NM_000016.5:c.875_876insCTT	NP_000007.1:p.Ala292_Gln293insLeu
NM_001127328.2:c.887_888insCTT	NP_001120800.1:p.Ala296_Gln297insLeu
NM_001286042.1:c.767_768insCTT	NP_001272971.1:p.Ala256_Gln257insLeu
NM_001286043.1:c.974_975insCTT	NP_001272972.1:p.Ala325_Gln326insLeu
NM_001286044.1:c.308_309insCTT	NP_001272973.1:p.Ala103_Gln104insLeu
NM_000016.6:c.875_876insCTT MANE Select	NP_000007.1:p.Ala292_Gln293insLeu
NM_001127328.3:c.887_888insCTT	NP_001120800.1:p.Ala296_Gln297insLeu
NM_001286042.2:c.767_768insCTT	NP_001272971.1:p.Ala256_Gln257insLeu
NM_001286043.2:c.974_975insCTT	NP_001272972.1:p.Ala325_Gln326insLeu
NM_001286044.2:c.308_309insCTT	NP_001272973.1:p.Ala103_Gln104insLeu