Canonical Allele Identifier: CA418539943

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76205736A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75740051A>C , CM000663.2:g.75740051A>C	GRCh38
NC_000001.10:g.76205736A>C , CM000663.1:g.76205736A>C	GRCh37
NC_000001.9:g.75978324A>C	NCBI36
NG_007045.2:g.20694A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.540A>C MANE Select	ENSP00000359878.5:p.Gly180=
ENST00000473018.3:n.2664A>C
ENST00000541113.6:c.540A>C	ENSP00000442324.2:p.Gly180=
ENST00000679509.1:n.1502A>C
ENST00000679530.1:c.*308A>C	ENSP00000506454.1:n.*308A>C
ENST00000679615.1:n.2664A>C
ENST00000679687.1:c.102A>C	ENSP00000506598.1:p.Gly34=
ENST00000679704.1:c.*306A>C	ENSP00000505117.1:n.*306A>C
ENST00000679709.1:c.*503A>C	ENSP00000506623.1:n.*503A>C
ENST00000679804.1:n.279A>C
ENST00000679976.1:c.*124A>C	ENSP00000505565.1:n.*124A>C
ENST00000680166.1:n.3829A>C
ENST00000680517.1:c.*37A>C	ENSP00000505803.1:n.*37A>C
ENST00000680582.1:n.1502A>C
ENST00000680613.1:c.540A>C	ENSP00000506114.1:p.Gly180=
ENST00000680662.1:c.*454A>C	ENSP00000505080.1:n.*454A>C
ENST00000680691.1:c.*203A>C	ENSP00000506487.1:n.*203A>C
ENST00000680694.1:c.*128A>C	ENSP00000505658.1:n.*128A>C
ENST00000680743.1:c.*207A>C	ENSP00000505073.1:n.*207A>C
ENST00000680749.1:c.540A>C	ENSP00000505122.1:p.Gly180=
ENST00000680798.1:c.*124A>C	ENSP00000505670.1:n.*124A>C
ENST00000680805.1:c.540A>C	ENSP00000505447.1:p.Gly180=
ENST00000680844.1:c.*324A>C	ENSP00000506541.1:n.*324A>C
ENST00000680948.1:c.*407A>C	ENSP00000505441.1:n.*407A>C
ENST00000680964.1:c.540A>C	ENSP00000505961.1:p.Gly180=
ENST00000681037.1:c.540A>C	ENSP00000506025.1:p.Gly180=
ENST00000681063.1:c.540A>C	ENSP00000506616.1:p.Gly180=
ENST00000681209.1:c.*304A>C	ENSP00000505877.1:n.*304A>C
ENST00000681278.1:n.897A>C
ENST00000681289.1:n.897A>C
ENST00000681361.1:c.*207A>C	ENSP00000506679.1:n.*207A>C
ENST00000681430.1:c.540A>C	ENSP00000506301.1:p.Gly180=
ENST00000681446.1:c.*122A>C	ENSP00000506244.1:n.*122A>C
ENST00000681450.1:c.*211A>C	ENSP00000505660.1:n.*211A>C
ENST00000681548.1:c.*126A>C	ENSP00000505275.1:n.*126A>C
ENST00000681616.1:c.*308A>C	ENSP00000505111.1:n.*308A>C
ENST00000681621.1:c.*124A>C	ENSP00000505770.1:n.*124A>C
ENST00000681680.1:n.2664A>C
ENST00000681720.1:c.*55-5755A>C	ENSP00000505438.1:n.*55-5755A>C
ENST00000681730.1:n.762A>C
ENST00000681790.1:c.282A>C	ENSP00000505130.1:p.Gly94=
ENST00000681837.1:n.1156A>C
ENST00000681913.1:n.2664A>C
ENST00000681916.1:c.*308A>C	ENSP00000506477.1:n.*308A>C
ENST00000681930.1:n.2664A>C
ENST00000370834.9:c.639A>C	ENSP00000359871.5:p.Gly213=
ENST00000370841.8:c.540A>C	ENSP00000359878.4:p.Gly180=
ENST00000420607.6:c.552A>C	ENSP00000409612.2:p.Gly184=
ENST00000525808.5:c.*126A>C	ENSP00000434823.1:n.*126A>C
ENST00000526129.5:c.*324A>C	ENSP00000434092.1:n.*324A>C
ENST00000526196.5:c.*308A>C	ENSP00000431953.1:n.*308A>C
ENST00000526930.1:n.313A>C
ENST00000529059.5:n.449A>C
ENST00000530953.6:c.*37A>C	ENSP00000431372.1:n.*37A>C
ENST00000532509.5:c.*304A>C	ENSP00000432522.1:n.*304A>C
ENST00000534334.5:c.*124A>C	ENSP00000435584.1:n.*124A>C
ENST00000541113.5:c.432A>C	ENSP00000442324.1:p.Gly144=
NM_000016.5:c.540A>C	NP_000007.1:p.Gly180=
NM_001127328.2:c.552A>C	NP_001120800.1:p.Gly184=
NM_001286042.1:c.432A>C	NP_001272971.1:p.Gly144=
NM_001286043.1:c.639A>C	NP_001272972.1:p.Gly213=
NM_001286044.1:c.-28A>C	NP_001272973.1:n.-28A>C
NM_000016.6:c.540A>C MANE Select	NP_000007.1:p.Gly180=
NM_001127328.3:c.552A>C	NP_001120800.1:p.Gly184=
NM_001286042.2:c.432A>C	NP_001272971.1:p.Gly144=
NM_001286043.2:c.639A>C	NP_001272972.1:p.Gly213=
NM_001286044.2:c.-28A>C	NP_001272973.1:n.-28A>C