Canonical Allele Identifier: CA340814912

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76205689G>T (hg19) ; chr1:g.75740004G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75740004G>T , CM000663.2:g.75740004G>T	GRCh38
NC_000001.10:g.76205689G>T , CM000663.1:g.76205689G>T	GRCh37
NC_000001.9:g.75978277G>T	NCBI36
NG_007045.2:g.20647G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.493G>T MANE Select	ENSP00000359878.5:p.Ala165Ser
ENST00000473018.3:n.2617G>T
ENST00000541113.6:c.493G>T	ENSP00000442324.2:p.Ala165Ser
ENST00000679509.1:n.1455G>T
ENST00000679530.1:c.*261G>T	ENSP00000506454.1:n.*261G>T
ENST00000679615.1:n.2617G>T
ENST00000679687.1:c.55G>T	ENSP00000506598.1:p.Ala19Ser
ENST00000679704.1:c.*259G>T	ENSP00000505117.1:n.*259G>T
ENST00000679709.1:c.*456G>T	ENSP00000506623.1:n.*456G>T
ENST00000679804.1:n.232G>T
ENST00000679976.1:c.*77G>T	ENSP00000505565.1:n.*77G>T
ENST00000680166.1:n.3782G>T
ENST00000680517.1:c.311G>T	ENSP00000505803.1:p.Ser104Ile
ENST00000680582.1:n.1455G>T
ENST00000680613.1:c.493G>T	ENSP00000506114.1:p.Ala165Ser
ENST00000680662.1:c.*407G>T	ENSP00000505080.1:n.*407G>T
ENST00000680691.1:c.*156G>T	ENSP00000506487.1:n.*156G>T
ENST00000680694.1:c.*81G>T	ENSP00000505658.1:n.*81G>T
ENST00000680743.1:c.*160G>T	ENSP00000505073.1:n.*160G>T
ENST00000680749.1:c.493G>T	ENSP00000505122.1:p.Ala165Ser
ENST00000680798.1:c.*77G>T	ENSP00000505670.1:n.*77G>T
ENST00000680805.1:c.493G>T	ENSP00000505447.1:p.Ala165Ser
ENST00000680844.1:c.*277G>T	ENSP00000506541.1:n.*277G>T
ENST00000680948.1:c.*360G>T	ENSP00000505441.1:n.*360G>T
ENST00000680964.1:c.493G>T	ENSP00000505961.1:p.Ala165Ser
ENST00000681037.1:c.493G>T	ENSP00000506025.1:p.Ala165Ser
ENST00000681063.1:c.493G>T	ENSP00000506616.1:p.Ala165Ser
ENST00000681209.1:c.*257G>T	ENSP00000505877.1:n.*257G>T
ENST00000681278.1:n.850G>T
ENST00000681289.1:n.850G>T
ENST00000681361.1:c.*160G>T	ENSP00000506679.1:n.*160G>T
ENST00000681430.1:c.493G>T	ENSP00000506301.1:p.Ala165Ser
ENST00000681446.1:c.*75G>T	ENSP00000506244.1:n.*75G>T
ENST00000681450.1:c.*164G>T	ENSP00000505660.1:n.*164G>T
ENST00000681548.1:c.*79G>T	ENSP00000505275.1:n.*79G>T
ENST00000681616.1:c.*261G>T	ENSP00000505111.1:n.*261G>T
ENST00000681621.1:c.*77G>T	ENSP00000505770.1:n.*77G>T
ENST00000681680.1:n.2617G>T
ENST00000681720.1:c.*55-5802G>T	ENSP00000505438.1:n.*55-5802G>T
ENST00000681730.1:n.715G>T
ENST00000681790.1:c.235G>T	ENSP00000505130.1:p.Ala79Ser
ENST00000681837.1:n.1109G>T
ENST00000681913.1:n.2617G>T
ENST00000681916.1:c.*261G>T	ENSP00000506477.1:n.*261G>T
ENST00000681930.1:n.2617G>T
ENST00000370834.9:c.592G>T	ENSP00000359871.5:p.Ala198Ser
ENST00000370841.8:c.493G>T	ENSP00000359878.4:p.Ala165Ser
ENST00000420607.6:c.505G>T	ENSP00000409612.2:p.Ala169Ser
ENST00000525808.5:c.*79G>T	ENSP00000434823.1:n.*79G>T
ENST00000526129.5:c.*277G>T	ENSP00000434092.1:n.*277G>T
ENST00000526196.5:c.*261G>T	ENSP00000431953.1:n.*261G>T
ENST00000526930.1:n.266G>T
ENST00000529059.5:n.402G>T
ENST00000530953.6:c.143G>T	ENSP00000431372.1:p.Ser48Ile
ENST00000532509.5:c.*257G>T	ENSP00000432522.1:n.*257G>T
ENST00000534334.5:c.*77G>T	ENSP00000435584.1:n.*77G>T
ENST00000541113.5:c.385G>T	ENSP00000442324.1:p.Ala129Ser
NM_000016.5:c.493G>T	NP_000007.1:p.Ala165Ser
NM_001127328.2:c.505G>T	NP_001120800.1:p.Ala169Ser
NM_001286042.1:c.385G>T	NP_001272971.1:p.Ala129Ser
NM_001286043.1:c.592G>T	NP_001272972.1:p.Ala198Ser
NM_001286044.1:c.-75G>T	NP_001272973.1:n.-75G>T
NM_000016.6:c.493G>T MANE Select	NP_000007.1:p.Ala165Ser
NM_001127328.3:c.505G>T	NP_001120800.1:p.Ala169Ser
NM_001286042.2:c.385G>T	NP_001272971.1:p.Ala129Ser
NM_001286043.2:c.592G>T	NP_001272972.1:p.Ala198Ser
NM_001286044.2:c.-75G>T	NP_001272973.1:n.-75G>T