Canonical Allele Identifier: CA340814946

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76205695T>G (hg19) ; chr1:g.75740010T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75740010T>G , CM000663.2:g.75740010T>G	GRCh38
NC_000001.10:g.76205695T>G , CM000663.1:g.76205695T>G	GRCh37
NC_000001.9:g.75978283T>G	NCBI36
NG_007045.2:g.20653T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.499T>G MANE Select	ENSP00000359878.5:p.Ser167Ala
ENST00000473018.3:n.2623T>G
ENST00000541113.6:c.499T>G	ENSP00000442324.2:p.Ser167Ala
ENST00000679509.1:n.1461T>G
ENST00000679530.1:c.*267T>G	ENSP00000506454.1:n.*267T>G
ENST00000679615.1:n.2623T>G
ENST00000679687.1:c.61T>G	ENSP00000506598.1:p.Ser21Ala
ENST00000679704.1:c.*265T>G	ENSP00000505117.1:n.*265T>G
ENST00000679709.1:c.*462T>G	ENSP00000506623.1:n.*462T>G
ENST00000679804.1:n.238T>G
ENST00000679976.1:c.*83T>G	ENSP00000505565.1:n.*83T>G
ENST00000680166.1:n.3788T>G
ENST00000680517.1:c.317T>G	ENSP00000505803.1:p.Leu106Arg
ENST00000680582.1:n.1461T>G
ENST00000680613.1:c.499T>G	ENSP00000506114.1:p.Ser167Ala
ENST00000680662.1:c.*413T>G	ENSP00000505080.1:n.*413T>G
ENST00000680691.1:c.*162T>G	ENSP00000506487.1:n.*162T>G
ENST00000680694.1:c.*87T>G	ENSP00000505658.1:n.*87T>G
ENST00000680743.1:c.*166T>G	ENSP00000505073.1:n.*166T>G
ENST00000680749.1:c.499T>G	ENSP00000505122.1:p.Ser167Ala
ENST00000680798.1:c.*83T>G	ENSP00000505670.1:n.*83T>G
ENST00000680805.1:c.499T>G	ENSP00000505447.1:p.Ser167Ala
ENST00000680844.1:c.*283T>G	ENSP00000506541.1:n.*283T>G
ENST00000680948.1:c.*366T>G	ENSP00000505441.1:n.*366T>G
ENST00000680964.1:c.499T>G	ENSP00000505961.1:p.Ser167Ala
ENST00000681037.1:c.499T>G	ENSP00000506025.1:p.Ser167Ala
ENST00000681063.1:c.499T>G	ENSP00000506616.1:p.Ser167Ala
ENST00000681209.1:c.*263T>G	ENSP00000505877.1:n.*263T>G
ENST00000681278.1:n.856T>G
ENST00000681289.1:n.856T>G
ENST00000681361.1:c.*166T>G	ENSP00000506679.1:n.*166T>G
ENST00000681430.1:c.499T>G	ENSP00000506301.1:p.Ser167Ala
ENST00000681446.1:c.*81T>G	ENSP00000506244.1:n.*81T>G
ENST00000681450.1:c.*170T>G	ENSP00000505660.1:n.*170T>G
ENST00000681548.1:c.*85T>G	ENSP00000505275.1:n.*85T>G
ENST00000681616.1:c.*267T>G	ENSP00000505111.1:n.*267T>G
ENST00000681621.1:c.*83T>G	ENSP00000505770.1:n.*83T>G
ENST00000681680.1:n.2623T>G
ENST00000681720.1:c.*55-5796T>G	ENSP00000505438.1:n.*55-5796T>G
ENST00000681730.1:n.721T>G
ENST00000681790.1:c.241T>G	ENSP00000505130.1:p.Ser81Ala
ENST00000681837.1:n.1115T>G
ENST00000681913.1:n.2623T>G
ENST00000681916.1:c.*267T>G	ENSP00000506477.1:n.*267T>G
ENST00000681930.1:n.2623T>G
ENST00000370834.9:c.598T>G	ENSP00000359871.5:p.Ser200Ala
ENST00000370841.8:c.499T>G	ENSP00000359878.4:p.Ser167Ala
ENST00000420607.6:c.511T>G	ENSP00000409612.2:p.Ser171Ala
ENST00000525808.5:c.*85T>G	ENSP00000434823.1:n.*85T>G
ENST00000526129.5:c.*283T>G	ENSP00000434092.1:n.*283T>G
ENST00000526196.5:c.*267T>G	ENSP00000431953.1:n.*267T>G
ENST00000526930.1:n.272T>G
ENST00000529059.5:n.408T>G
ENST00000530953.6:c.149T>G	ENSP00000431372.1:p.Leu50Arg
ENST00000532509.5:c.*263T>G	ENSP00000432522.1:n.*263T>G
ENST00000534334.5:c.*83T>G	ENSP00000435584.1:n.*83T>G
ENST00000541113.5:c.391T>G	ENSP00000442324.1:p.Ser131Ala
NM_000016.5:c.499T>G	NP_000007.1:p.Ser167Ala
NM_001127328.2:c.511T>G	NP_001120800.1:p.Ser171Ala
NM_001286042.1:c.391T>G	NP_001272971.1:p.Ser131Ala
NM_001286043.1:c.598T>G	NP_001272972.1:p.Ser200Ala
NM_001286044.1:c.-69T>G	NP_001272973.1:n.-69T>G
NM_000016.6:c.499T>G MANE Select	NP_000007.1:p.Ser167Ala
NM_001127328.3:c.511T>G	NP_001120800.1:p.Ser171Ala
NM_001286042.2:c.391T>G	NP_001272971.1:p.Ser131Ala
NM_001286043.2:c.598T>G	NP_001272972.1:p.Ser200Ala
NM_001286044.2:c.-69T>G	NP_001272973.1:n.-69T>G