Canonical Allele Identifier: CA418707627

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226926T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761241T>C , CM000663.2:g.75761241T>C	GRCh38
NC_000001.10:g.76226926T>C , CM000663.1:g.76226926T>C	GRCh37
NC_000001.9:g.75999514T>C	NCBI36
NG_007045.2:g.41884T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.1065T>C MANE Select	ENSP00000359878.5:p.Ser355=
ENST00000473018.3:n.3189T>C
ENST00000532207.6:n.2076T>C
ENST00000541113.6:c.969T>C	ENSP00000442324.2:p.Ser323=
ENST00000679509.1:n.2027T>C
ENST00000679530.1:c.*833T>C	ENSP00000506454.1:n.*833T>C
ENST00000679615.1:n.3080T>C
ENST00000679687.1:c.627T>C	ENSP00000506598.1:p.Ser209=
ENST00000679704.1:c.*831T>C	ENSP00000505117.1:n.*831T>C
ENST00000679709.1:c.*1028T>C	ENSP00000506623.1:n.*1028T>C
ENST00000679976.1:c.*649T>C	ENSP00000505565.1:n.*649T>C
ENST00000680166.1:n.4354T>C
ENST00000680315.1:n.948T>C
ENST00000680517.1:c.*453T>C	ENSP00000505803.1:n.*453T>C
ENST00000680582.1:n.2027T>C
ENST00000680613.1:c.*558T>C	ENSP00000506114.1:n.*558T>C
ENST00000680662.1:c.*979T>C	ENSP00000505080.1:n.*979T>C
ENST00000680691.1:c.*728T>C	ENSP00000506487.1:n.*728T>C
ENST00000680694.1:c.*653T>C	ENSP00000505658.1:n.*653T>C
ENST00000680743.1:c.*854T>C	ENSP00000505073.1:n.*854T>C
ENST00000680749.1:c.*350T>C	ENSP00000505122.1:n.*350T>C
ENST00000680798.1:c.*540T>C	ENSP00000505670.1:n.*540T>C
ENST00000680805.1:c.924T>C	ENSP00000505447.1:p.Ser308=
ENST00000680844.1:c.*849T>C	ENSP00000506541.1:n.*849T>C
ENST00000680948.1:c.*932T>C	ENSP00000505441.1:n.*932T>C
ENST00000680964.1:c.*158T>C	ENSP00000505961.1:n.*158T>C
ENST00000681037.1:c.*2549T>C	ENSP00000506025.1:n.*2549T>C
ENST00000681063.1:c.*334T>C	ENSP00000506616.1:n.*334T>C
ENST00000681209.1:c.*720T>C	ENSP00000505877.1:n.*720T>C
ENST00000681278.1:n.1767T>C
ENST00000681289.1:n.5060T>C
ENST00000681361.1:c.*732T>C	ENSP00000506679.1:n.*732T>C
ENST00000681430.1:c.*158T>C	ENSP00000506301.1:n.*158T>C
ENST00000681446.1:c.*769T>C	ENSP00000506244.1:n.*769T>C
ENST00000681450.1:c.*736T>C	ENSP00000505660.1:n.*736T>C
ENST00000681548.1:c.*651T>C	ENSP00000505275.1:n.*651T>C
ENST00000681616.1:c.*724T>C	ENSP00000505111.1:n.*724T>C
ENST00000681621.1:c.*649T>C	ENSP00000505770.1:n.*649T>C
ENST00000681680.1:n.3160T>C
ENST00000681720.1:c.*520T>C	ENSP00000505438.1:n.*520T>C
ENST00000681730.1:n.1287T>C
ENST00000681790.1:c.807T>C	ENSP00000505130.1:p.Ser269=
ENST00000681837.1:n.1681T>C
ENST00000681913.1:n.3311T>C
ENST00000681916.1:c.*833T>C	ENSP00000506477.1:n.*833T>C
ENST00000681930.1:n.3189T>C
ENST00000370834.9:c.1164T>C	ENSP00000359871.5:p.Ser388=
ENST00000370841.8:c.1065T>C	ENSP00000359878.4:p.Ser355=
ENST00000420607.6:c.1077T>C	ENSP00000409612.2:p.Ser359=
ENST00000481374.1:n.338T>C
ENST00000525808.5:c.*651T>C	ENSP00000434823.1:n.*651T>C
ENST00000526129.5:c.*849T>C	ENSP00000434092.1:n.*849T>C
ENST00000526196.5:c.*833T>C	ENSP00000431953.1:n.*833T>C
ENST00000528016.1:c.160-7936T>C	ENSP00000434284.1:n.160-7936T>C
ENST00000529059.5:n.974T>C
ENST00000534334.5:c.*806T>C	ENSP00000435584.1:n.*806T>C
ENST00000541113.5:c.957T>C	ENSP00000442324.1:p.Ser319=
NM_000016.5:c.1065T>C	NP_000007.1:p.Ser355=
NM_001127328.2:c.1077T>C	NP_001120800.1:p.Ser359=
NM_001286042.1:c.957T>C	NP_001272971.1:p.Ser319=
NM_001286043.1:c.1164T>C	NP_001272972.1:p.Ser388=
NM_001286044.1:c.498T>C	NP_001272973.1:p.Ser166=
NM_000016.6:c.1065T>C MANE Select	NP_000007.1:p.Ser355=
NM_001127328.3:c.1077T>C	NP_001120800.1:p.Ser359=
NM_001286042.2:c.957T>C	NP_001272971.1:p.Ser319=
NM_001286043.2:c.1164T>C	NP_001272972.1:p.Ser388=
NM_001286044.2:c.498T>C	NP_001272973.1:p.Ser166=