Canonical Allele Identifier: CA418707534

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226869T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761184T>C , CM000663.2:g.75761184T>C	GRCh38
NC_000001.10:g.76226869T>C , CM000663.1:g.76226869T>C	GRCh37
NC_000001.9:g.75999457T>C	NCBI36
NG_007045.2:g.41827T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.1008T>C MANE Select	ENSP00000359878.5:p.Ser336=
ENST00000473018.3:n.3132T>C
ENST00000532207.6:n.2019T>C
ENST00000541113.6:c.912T>C	ENSP00000442324.2:p.Ser304=
ENST00000679509.1:n.1970T>C
ENST00000679530.1:c.*776T>C	ENSP00000506454.1:n.*776T>C
ENST00000679615.1:n.3023T>C
ENST00000679687.1:c.570T>C	ENSP00000506598.1:p.Ser190=
ENST00000679704.1:c.*774T>C	ENSP00000505117.1:n.*774T>C
ENST00000679709.1:c.*971T>C	ENSP00000506623.1:n.*971T>C
ENST00000679976.1:c.*592T>C	ENSP00000505565.1:n.*592T>C
ENST00000680166.1:n.4297T>C
ENST00000680315.1:n.891T>C
ENST00000680517.1:c.*396T>C	ENSP00000505803.1:n.*396T>C
ENST00000680582.1:n.1970T>C
ENST00000680613.1:c.*501T>C	ENSP00000506114.1:n.*501T>C
ENST00000680662.1:c.*922T>C	ENSP00000505080.1:n.*922T>C
ENST00000680691.1:c.*671T>C	ENSP00000506487.1:n.*671T>C
ENST00000680694.1:c.*596T>C	ENSP00000505658.1:n.*596T>C
ENST00000680743.1:c.*797T>C	ENSP00000505073.1:n.*797T>C
ENST00000680749.1:c.*293T>C	ENSP00000505122.1:n.*293T>C
ENST00000680798.1:c.*483T>C	ENSP00000505670.1:n.*483T>C
ENST00000680805.1:c.867T>C	ENSP00000505447.1:p.Ser289=
ENST00000680844.1:c.*792T>C	ENSP00000506541.1:n.*792T>C
ENST00000680948.1:c.*875T>C	ENSP00000505441.1:n.*875T>C
ENST00000680964.1:c.*101T>C	ENSP00000505961.1:n.*101T>C
ENST00000681037.1:c.*2492T>C	ENSP00000506025.1:n.*2492T>C
ENST00000681063.1:c.*277T>C	ENSP00000506616.1:n.*277T>C
ENST00000681209.1:c.*663T>C	ENSP00000505877.1:n.*663T>C
ENST00000681278.1:n.1710T>C
ENST00000681289.1:n.5003T>C
ENST00000681361.1:c.*675T>C	ENSP00000506679.1:n.*675T>C
ENST00000681430.1:c.*101T>C	ENSP00000506301.1:n.*101T>C
ENST00000681446.1:c.*712T>C	ENSP00000506244.1:n.*712T>C
ENST00000681450.1:c.*679T>C	ENSP00000505660.1:n.*679T>C
ENST00000681548.1:c.*594T>C	ENSP00000505275.1:n.*594T>C
ENST00000681616.1:c.*667T>C	ENSP00000505111.1:n.*667T>C
ENST00000681621.1:c.*592T>C	ENSP00000505770.1:n.*592T>C
ENST00000681680.1:n.3103T>C
ENST00000681720.1:c.*463T>C	ENSP00000505438.1:n.*463T>C
ENST00000681730.1:n.1230T>C
ENST00000681790.1:c.750T>C	ENSP00000505130.1:p.Ser250=
ENST00000681837.1:n.1624T>C
ENST00000681913.1:n.3254T>C
ENST00000681916.1:c.*776T>C	ENSP00000506477.1:n.*776T>C
ENST00000681930.1:n.3132T>C
ENST00000370834.9:c.1107T>C	ENSP00000359871.5:p.Ser369=
ENST00000370841.8:c.1008T>C	ENSP00000359878.4:p.Ser336=
ENST00000420607.6:c.1020T>C	ENSP00000409612.2:p.Ser340=
ENST00000481374.1:n.281T>C
ENST00000525808.5:c.*594T>C	ENSP00000434823.1:n.*594T>C
ENST00000526129.5:c.*792T>C	ENSP00000434092.1:n.*792T>C
ENST00000526196.5:c.*776T>C	ENSP00000431953.1:n.*776T>C
ENST00000528016.1:c.160-7993T>C	ENSP00000434284.1:n.160-7993T>C
ENST00000529059.5:n.917T>C
ENST00000532207.5:n.738T>C
ENST00000534334.5:c.*749T>C	ENSP00000435584.1:n.*749T>C
ENST00000541113.5:c.900T>C	ENSP00000442324.1:p.Ser300=
NM_000016.5:c.1008T>C	NP_000007.1:p.Ser336=
NM_001127328.2:c.1020T>C	NP_001120800.1:p.Ser340=
NM_001286042.1:c.900T>C	NP_001272971.1:p.Ser300=
NM_001286043.1:c.1107T>C	NP_001272972.1:p.Ser369=
NM_001286044.1:c.441T>C	NP_001272973.1:p.Ser147=
NM_000016.6:c.1008T>C MANE Select	NP_000007.1:p.Ser336=
NM_001127328.3:c.1020T>C	NP_001120800.1:p.Ser340=
NM_001286042.2:c.900T>C	NP_001272971.1:p.Ser300=
NM_001286043.2:c.1107T>C	NP_001272972.1:p.Ser369=
NM_001286044.2:c.441T>C	NP_001272973.1:p.Ser147=