Canonical Allele Identifier: CA418707748

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226995C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761310C>G , CM000663.2:g.75761310C>G	GRCh38
NC_000001.10:g.76226995C>G , CM000663.1:g.76226995C>G	GRCh37
NC_000001.9:g.75999583C>G	NCBI36
NG_007045.2:g.41953C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.1134C>G MANE Select	ENSP00000359878.5:p.Gly378=
ENST00000473018.3:n.3258C>G
ENST00000532207.6:n.2145C>G
ENST00000541113.6:c.1038C>G	ENSP00000442324.2:p.Gly346=
ENST00000679509.1:n.2096C>G
ENST00000679530.1:c.*902C>G	ENSP00000506454.1:n.*902C>G
ENST00000679615.1:n.3149C>G
ENST00000679687.1:c.696C>G	ENSP00000506598.1:p.Gly232=
ENST00000679704.1:c.*900C>G	ENSP00000505117.1:n.*900C>G
ENST00000679709.1:c.*1097C>G	ENSP00000506623.1:n.*1097C>G
ENST00000679976.1:c.*718C>G	ENSP00000505565.1:n.*718C>G
ENST00000680166.1:n.4423C>G
ENST00000680315.1:n.1017C>G
ENST00000680517.1:c.*522C>G	ENSP00000505803.1:n.*522C>G
ENST00000680582.1:n.2096C>G
ENST00000680613.1:c.*627C>G	ENSP00000506114.1:n.*627C>G
ENST00000680662.1:c.*1048C>G	ENSP00000505080.1:n.*1048C>G
ENST00000680691.1:c.*797C>G	ENSP00000506487.1:n.*797C>G
ENST00000680694.1:c.*722C>G	ENSP00000505658.1:n.*722C>G
ENST00000680743.1:c.*923C>G	ENSP00000505073.1:n.*923C>G
ENST00000680749.1:c.*419C>G	ENSP00000505122.1:n.*419C>G
ENST00000680798.1:c.*609C>G	ENSP00000505670.1:n.*609C>G
ENST00000680805.1:c.993C>G	ENSP00000505447.1:p.Gly331=
ENST00000680844.1:c.*918C>G	ENSP00000506541.1:n.*918C>G
ENST00000680948.1:c.*1001C>G	ENSP00000505441.1:n.*1001C>G
ENST00000680964.1:c.*227C>G	ENSP00000505961.1:n.*227C>G
ENST00000681037.1:c.*2618C>G	ENSP00000506025.1:n.*2618C>G
ENST00000681063.1:c.*403C>G	ENSP00000506616.1:n.*403C>G
ENST00000681209.1:c.*789C>G	ENSP00000505877.1:n.*789C>G
ENST00000681278.1:n.1836C>G
ENST00000681289.1:n.5129C>G
ENST00000681361.1:c.*801C>G	ENSP00000506679.1:n.*801C>G
ENST00000681430.1:c.*227C>G	ENSP00000506301.1:n.*227C>G
ENST00000681446.1:c.*838C>G	ENSP00000506244.1:n.*838C>G
ENST00000681450.1:c.*805C>G	ENSP00000505660.1:n.*805C>G
ENST00000681548.1:c.*720C>G	ENSP00000505275.1:n.*720C>G
ENST00000681616.1:c.*793C>G	ENSP00000505111.1:n.*793C>G
ENST00000681621.1:c.*718C>G	ENSP00000505770.1:n.*718C>G
ENST00000681680.1:n.3229C>G
ENST00000681720.1:c.*589C>G	ENSP00000505438.1:n.*589C>G
ENST00000681730.1:n.1356C>G
ENST00000681790.1:c.876C>G	ENSP00000505130.1:p.Gly292=
ENST00000681837.1:n.1750C>G
ENST00000681913.1:n.3380C>G
ENST00000681916.1:c.*902C>G	ENSP00000506477.1:n.*902C>G
ENST00000681930.1:n.3258C>G
ENST00000370834.9:c.1233C>G	ENSP00000359871.5:p.Gly411=
ENST00000370841.8:c.1134C>G	ENSP00000359878.4:p.Gly378=
ENST00000420607.6:c.1146C>G	ENSP00000409612.2:p.Gly382=
ENST00000481374.1:n.407C>G
ENST00000525808.5:c.*720C>G	ENSP00000434823.1:n.*720C>G
ENST00000526129.5:c.*918C>G	ENSP00000434092.1:n.*918C>G
ENST00000526196.5:c.*902C>G	ENSP00000431953.1:n.*902C>G
ENST00000528016.1:c.160-7867C>G	ENSP00000434284.1:n.160-7867C>G
ENST00000529059.5:n.1043C>G
ENST00000541113.5:c.1026C>G	ENSP00000442324.1:p.Gly342=
NM_000016.5:c.1134C>G	NP_000007.1:p.Gly378=
NM_001127328.2:c.1146C>G	NP_001120800.1:p.Gly382=
NM_001286042.1:c.1026C>G	NP_001272971.1:p.Gly342=
NM_001286043.1:c.1233C>G	NP_001272972.1:p.Gly411=
NM_001286044.1:c.567C>G	NP_001272973.1:p.Gly189=
NM_000016.6:c.1134C>G MANE Select	NP_000007.1:p.Gly378=
NM_001127328.3:c.1146C>G	NP_001120800.1:p.Gly382=
NM_001286042.2:c.1026C>G	NP_001272971.1:p.Gly342=
NM_001286043.2:c.1233C>G	NP_001272972.1:p.Gly411=
NM_001286044.2:c.567C>G	NP_001272973.1:p.Gly189=