Canonical Allele Identifier: CA340818191

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226972G>A (hg19) ; chr1:g.75761287G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761287G>A , CM000663.2:g.75761287G>A	GRCh38
NC_000001.10:g.76226972G>A , CM000663.1:g.76226972G>A	GRCh37
NC_000001.9:g.75999560G>A	NCBI36
NG_007045.2:g.41930G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.1111G>A MANE Select	ENSP00000359878.5:p.Asp371Asn
ENST00000473018.3:n.3235G>A
ENST00000532207.6:n.2122G>A
ENST00000541113.6:c.1015G>A	ENSP00000442324.2:p.Asp339Asn
ENST00000679509.1:n.2073G>A
ENST00000679530.1:c.*879G>A	ENSP00000506454.1:n.*879G>A
ENST00000679615.1:n.3126G>A
ENST00000679687.1:c.673G>A	ENSP00000506598.1:p.Asp225Asn
ENST00000679704.1:c.*877G>A	ENSP00000505117.1:n.*877G>A
ENST00000679709.1:c.*1074G>A	ENSP00000506623.1:n.*1074G>A
ENST00000679976.1:c.*695G>A	ENSP00000505565.1:n.*695G>A
ENST00000680166.1:n.4400G>A
ENST00000680315.1:n.994G>A
ENST00000680517.1:c.*499G>A	ENSP00000505803.1:n.*499G>A
ENST00000680582.1:n.2073G>A
ENST00000680613.1:c.*604G>A	ENSP00000506114.1:n.*604G>A
ENST00000680662.1:c.*1025G>A	ENSP00000505080.1:n.*1025G>A
ENST00000680691.1:c.*774G>A	ENSP00000506487.1:n.*774G>A
ENST00000680694.1:c.*699G>A	ENSP00000505658.1:n.*699G>A
ENST00000680743.1:c.*900G>A	ENSP00000505073.1:n.*900G>A
ENST00000680749.1:c.*396G>A	ENSP00000505122.1:n.*396G>A
ENST00000680798.1:c.*586G>A	ENSP00000505670.1:n.*586G>A
ENST00000680805.1:c.970G>A	ENSP00000505447.1:p.Asp324Asn
ENST00000680844.1:c.*895G>A	ENSP00000506541.1:n.*895G>A
ENST00000680948.1:c.*978G>A	ENSP00000505441.1:n.*978G>A
ENST00000680964.1:c.*204G>A	ENSP00000505961.1:n.*204G>A
ENST00000681037.1:c.*2595G>A	ENSP00000506025.1:n.*2595G>A
ENST00000681063.1:c.*380G>A	ENSP00000506616.1:n.*380G>A
ENST00000681209.1:c.*766G>A	ENSP00000505877.1:n.*766G>A
ENST00000681278.1:n.1813G>A
ENST00000681289.1:n.5106G>A
ENST00000681361.1:c.*778G>A	ENSP00000506679.1:n.*778G>A
ENST00000681430.1:c.*204G>A	ENSP00000506301.1:n.*204G>A
ENST00000681446.1:c.*815G>A	ENSP00000506244.1:n.*815G>A
ENST00000681450.1:c.*782G>A	ENSP00000505660.1:n.*782G>A
ENST00000681548.1:c.*697G>A	ENSP00000505275.1:n.*697G>A
ENST00000681616.1:c.*770G>A	ENSP00000505111.1:n.*770G>A
ENST00000681621.1:c.*695G>A	ENSP00000505770.1:n.*695G>A
ENST00000681680.1:n.3206G>A
ENST00000681720.1:c.*566G>A	ENSP00000505438.1:n.*566G>A
ENST00000681730.1:n.1333G>A
ENST00000681790.1:c.853G>A	ENSP00000505130.1:p.Asp285Asn
ENST00000681837.1:n.1727G>A
ENST00000681913.1:n.3357G>A
ENST00000681916.1:c.*879G>A	ENSP00000506477.1:n.*879G>A
ENST00000681930.1:n.3235G>A
ENST00000370834.9:c.1210G>A	ENSP00000359871.5:p.Asp404Asn
ENST00000370841.8:c.1111G>A	ENSP00000359878.4:p.Asp371Asn
ENST00000420607.6:c.1123G>A	ENSP00000409612.2:p.Asp375Asn
ENST00000481374.1:n.384G>A
ENST00000525808.5:c.*697G>A	ENSP00000434823.1:n.*697G>A
ENST00000526129.5:c.*895G>A	ENSP00000434092.1:n.*895G>A
ENST00000526196.5:c.*879G>A	ENSP00000431953.1:n.*879G>A
ENST00000528016.1:c.160-7890G>A	ENSP00000434284.1:n.160-7890G>A
ENST00000529059.5:n.1020G>A
ENST00000541113.5:c.1003G>A	ENSP00000442324.1:p.Asp335Asn
NM_000016.5:c.1111G>A	NP_000007.1:p.Asp371Asn
NM_001127328.2:c.1123G>A	NP_001120800.1:p.Asp375Asn
NM_001286042.1:c.1003G>A	NP_001272971.1:p.Asp335Asn
NM_001286043.1:c.1210G>A	NP_001272972.1:p.Asp404Asn
NM_001286044.1:c.544G>A	NP_001272973.1:p.Asp182Asn
NM_000016.6:c.1111G>A MANE Select	NP_000007.1:p.Asp371Asn
NM_001127328.3:c.1123G>A	NP_001120800.1:p.Asp375Asn
NM_001286042.2:c.1003G>A	NP_001272971.1:p.Asp335Asn
NM_001286043.2:c.1210G>A	NP_001272972.1:p.Asp404Asn
NM_001286044.2:c.544G>A	NP_001272973.1:p.Asp182Asn