Canonical Allele Identifier: CA418530633

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226821A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761136A>T , CM000663.2:g.75761136A>T	GRCh38
NC_000001.10:g.76226821A>T , CM000663.1:g.76226821A>T	GRCh37
NC_000001.9:g.75999409A>T	NCBI36
NG_007045.2:g.41779A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.960A>T MANE Select	ENSP00000359878.5:p.Ser320=
ENST00000473018.3:n.3084A>T
ENST00000532207.6:n.1971A>T
ENST00000541113.6:c.864A>T	ENSP00000442324.2:p.Ser288=
ENST00000679509.1:n.1922A>T
ENST00000679530.1:c.*728A>T	ENSP00000506454.1:n.*728A>T
ENST00000679615.1:n.2975A>T
ENST00000679687.1:c.522A>T	ENSP00000506598.1:p.Ser174=
ENST00000679704.1:c.*726A>T	ENSP00000505117.1:n.*726A>T
ENST00000679709.1:c.*923A>T	ENSP00000506623.1:n.*923A>T
ENST00000679976.1:c.*544A>T	ENSP00000505565.1:n.*544A>T
ENST00000680166.1:n.4249A>T
ENST00000680315.1:n.843A>T
ENST00000680517.1:c.*348A>T	ENSP00000505803.1:n.*348A>T
ENST00000680582.1:n.1922A>T
ENST00000680613.1:c.*453A>T	ENSP00000506114.1:n.*453A>T
ENST00000680662.1:c.*874A>T	ENSP00000505080.1:n.*874A>T
ENST00000680691.1:c.*623A>T	ENSP00000506487.1:n.*623A>T
ENST00000680694.1:c.*548A>T	ENSP00000505658.1:n.*548A>T
ENST00000680743.1:c.*749A>T	ENSP00000505073.1:n.*749A>T
ENST00000680749.1:c.*245A>T	ENSP00000505122.1:n.*245A>T
ENST00000680798.1:c.*435A>T	ENSP00000505670.1:n.*435A>T
ENST00000680805.1:c.819A>T	ENSP00000505447.1:p.Ser273=
ENST00000680844.1:c.*744A>T	ENSP00000506541.1:n.*744A>T
ENST00000680948.1:c.*827A>T	ENSP00000505441.1:n.*827A>T
ENST00000680964.1:c.*53A>T	ENSP00000505961.1:n.*53A>T
ENST00000681037.1:c.*2444A>T	ENSP00000506025.1:n.*2444A>T
ENST00000681063.1:c.*229A>T	ENSP00000506616.1:n.*229A>T
ENST00000681209.1:c.*615A>T	ENSP00000505877.1:n.*615A>T
ENST00000681278.1:n.1662A>T
ENST00000681289.1:n.4955A>T
ENST00000681361.1:c.*627A>T	ENSP00000506679.1:n.*627A>T
ENST00000681430.1:c.*53A>T	ENSP00000506301.1:n.*53A>T
ENST00000681446.1:c.*664A>T	ENSP00000506244.1:n.*664A>T
ENST00000681450.1:c.*631A>T	ENSP00000505660.1:n.*631A>T
ENST00000681548.1:c.*546A>T	ENSP00000505275.1:n.*546A>T
ENST00000681616.1:c.*619A>T	ENSP00000505111.1:n.*619A>T
ENST00000681621.1:c.*544A>T	ENSP00000505770.1:n.*544A>T
ENST00000681680.1:n.3055A>T
ENST00000681720.1:c.*415A>T	ENSP00000505438.1:n.*415A>T
ENST00000681730.1:n.1182A>T
ENST00000681790.1:c.702A>T	ENSP00000505130.1:p.Ser234=
ENST00000681837.1:n.1576A>T
ENST00000681913.1:n.3206A>T
ENST00000681916.1:c.*728A>T	ENSP00000506477.1:n.*728A>T
ENST00000681930.1:n.3084A>T
ENST00000370834.9:c.1059A>T	ENSP00000359871.5:p.Ser353=
ENST00000370841.8:c.960A>T	ENSP00000359878.4:p.Ser320=
ENST00000420607.6:c.972A>T	ENSP00000409612.2:p.Ser324=
ENST00000481374.1:n.233A>T
ENST00000525808.5:c.*546A>T	ENSP00000434823.1:n.*546A>T
ENST00000526129.5:c.*744A>T	ENSP00000434092.1:n.*744A>T
ENST00000526196.5:c.*728A>T	ENSP00000431953.1:n.*728A>T
ENST00000528016.1:c.160-8041A>T	ENSP00000434284.1:n.160-8041A>T
ENST00000529059.5:n.869A>T
ENST00000532207.5:n.690A>T
ENST00000534334.5:c.*701A>T	ENSP00000435584.1:n.*701A>T
ENST00000541113.5:c.852A>T	ENSP00000442324.1:p.Ser284=
NM_000016.5:c.960A>T	NP_000007.1:p.Ser320=
NM_001127328.2:c.972A>T	NP_001120800.1:p.Ser324=
NM_001286042.1:c.852A>T	NP_001272971.1:p.Ser284=
NM_001286043.1:c.1059A>T	NP_001272972.1:p.Ser353=
NM_001286044.1:c.393A>T	NP_001272973.1:p.Ser131=
NM_000016.6:c.960A>T MANE Select	NP_000007.1:p.Ser320=
NM_001127328.3:c.972A>T	NP_001120800.1:p.Ser324=
NM_001286042.2:c.852A>T	NP_001272971.1:p.Ser284=
NM_001286043.2:c.1059A>T	NP_001272972.1:p.Ser353=
NM_001286044.2:c.393A>T	NP_001272973.1:p.Ser131=