Canonical Allele Identifier: CA340818245

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226999G>T (hg19) ; chr1:g.75761314G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761314G>T , CM000663.2:g.75761314G>T	GRCh38
NC_000001.10:g.76226999G>T , CM000663.1:g.76226999G>T	GRCh37
NC_000001.9:g.75999587G>T	NCBI36
NG_007045.2:g.41957G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.1138G>T MANE Select	ENSP00000359878.5:p.Gly380Ter
ENST00000473018.3:n.3262G>T
ENST00000532207.6:n.2149G>T
ENST00000541113.6:c.1042G>T	ENSP00000442324.2:p.Gly348Ter
ENST00000679509.1:n.2100G>T
ENST00000679530.1:c.*906G>T	ENSP00000506454.1:n.*906G>T
ENST00000679615.1:n.3153G>T
ENST00000679687.1:c.700G>T	ENSP00000506598.1:p.Gly234Ter
ENST00000679704.1:c.*904G>T	ENSP00000505117.1:n.*904G>T
ENST00000679709.1:c.*1101G>T	ENSP00000506623.1:n.*1101G>T
ENST00000679976.1:c.*722G>T	ENSP00000505565.1:n.*722G>T
ENST00000680166.1:n.4427G>T
ENST00000680315.1:n.1021G>T
ENST00000680517.1:c.*526G>T	ENSP00000505803.1:n.*526G>T
ENST00000680582.1:n.2100G>T
ENST00000680613.1:c.*631G>T	ENSP00000506114.1:n.*631G>T
ENST00000680662.1:c.*1052G>T	ENSP00000505080.1:n.*1052G>T
ENST00000680691.1:c.*801G>T	ENSP00000506487.1:n.*801G>T
ENST00000680694.1:c.*726G>T	ENSP00000505658.1:n.*726G>T
ENST00000680743.1:c.*927G>T	ENSP00000505073.1:n.*927G>T
ENST00000680749.1:c.*423G>T	ENSP00000505122.1:n.*423G>T
ENST00000680798.1:c.*613G>T	ENSP00000505670.1:n.*613G>T
ENST00000680805.1:c.997G>T	ENSP00000505447.1:p.Gly333Ter
ENST00000680844.1:c.*922G>T	ENSP00000506541.1:n.*922G>T
ENST00000680948.1:c.*1005G>T	ENSP00000505441.1:n.*1005G>T
ENST00000680964.1:c.*231G>T	ENSP00000505961.1:n.*231G>T
ENST00000681037.1:c.*2622G>T	ENSP00000506025.1:n.*2622G>T
ENST00000681063.1:c.*407G>T	ENSP00000506616.1:n.*407G>T
ENST00000681209.1:c.*793G>T	ENSP00000505877.1:n.*793G>T
ENST00000681278.1:n.1840G>T
ENST00000681289.1:n.5133G>T
ENST00000681361.1:c.*805G>T	ENSP00000506679.1:n.*805G>T
ENST00000681430.1:c.*231G>T	ENSP00000506301.1:n.*231G>T
ENST00000681446.1:c.*842G>T	ENSP00000506244.1:n.*842G>T
ENST00000681450.1:c.*809G>T	ENSP00000505660.1:n.*809G>T
ENST00000681548.1:c.*724G>T	ENSP00000505275.1:n.*724G>T
ENST00000681616.1:c.*797G>T	ENSP00000505111.1:n.*797G>T
ENST00000681621.1:c.*722G>T	ENSP00000505770.1:n.*722G>T
ENST00000681680.1:n.3233G>T
ENST00000681720.1:c.*593G>T	ENSP00000505438.1:n.*593G>T
ENST00000681730.1:n.1360G>T
ENST00000681790.1:c.880G>T	ENSP00000505130.1:p.Gly294Ter
ENST00000681837.1:n.1754G>T
ENST00000681913.1:n.3384G>T
ENST00000681916.1:c.*906G>T	ENSP00000506477.1:n.*906G>T
ENST00000681930.1:n.3262G>T
ENST00000370834.9:c.1237G>T	ENSP00000359871.5:p.Gly413Ter
ENST00000370841.8:c.1138G>T	ENSP00000359878.4:p.Gly380Ter
ENST00000420607.6:c.1150G>T	ENSP00000409612.2:p.Gly384Ter
ENST00000481374.1:n.411G>T
ENST00000525808.5:c.*724G>T	ENSP00000434823.1:n.*724G>T
ENST00000526129.5:c.*922G>T	ENSP00000434092.1:n.*922G>T
ENST00000526196.5:c.*906G>T	ENSP00000431953.1:n.*906G>T
ENST00000528016.1:c.160-7863G>T	ENSP00000434284.1:n.160-7863G>T
ENST00000529059.5:n.1047G>T
ENST00000541113.5:c.1030G>T	ENSP00000442324.1:p.Gly344Ter
NM_000016.5:c.1138G>T	NP_000007.1:p.Gly380Ter
NM_001127328.2:c.1150G>T	NP_001120800.1:p.Gly384Ter
NM_001286042.1:c.1030G>T	NP_001272971.1:p.Gly344Ter
NM_001286043.1:c.1237G>T	NP_001272972.1:p.Gly413Ter
NM_001286044.1:c.571G>T	NP_001272973.1:p.Gly191Ter
NM_000016.6:c.1138G>T MANE Select	NP_000007.1:p.Gly380Ter
NM_001127328.3:c.1150G>T	NP_001120800.1:p.Gly384Ter
NM_001286042.2:c.1030G>T	NP_001272971.1:p.Gly344Ter
NM_001286043.2:c.1237G>T	NP_001272972.1:p.Gly413Ter
NM_001286044.2:c.571G>T	NP_001272973.1:p.Gly191Ter