Canonical Allele Identifier: CA418531892

Gene: ACADM

Linked Data

• dbSNP Id: rs1436157528
• MyVariant Identifiers: chr1:g.76228412T>C (hg19) ; chr1:g.75762727T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75762727T>C , CM000663.2:g.75762727T>C	GRCh38
NC_000001.10:g.76228412T>C , CM000663.1:g.76228412T>C	GRCh37
NC_000001.9:g.76001000T>C	NCBI36
NG_007045.2:g.43370T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.1230T>C MANE Select	ENSP00000359878.5:p.Ile410=
ENST00000473018.3:n.3354T>C
ENST00000532207.6:n.3562T>C
ENST00000541113.6:c.1134T>C	ENSP00000442324.2:p.Ile378=
ENST00000679509.1:n.3513T>C
ENST00000679530.1:c.*998T>C	ENSP00000506454.1:n.*998T>C
ENST00000679615.1:n.4566T>C
ENST00000679687.1:c.792T>C	ENSP00000506598.1:p.Ile264=
ENST00000679704.1:c.*996T>C	ENSP00000505117.1:n.*996T>C
ENST00000679709.1:c.*1193T>C	ENSP00000506623.1:n.*1193T>C
ENST00000679976.1:c.*814T>C	ENSP00000505565.1:n.*814T>C
ENST00000680166.1:n.4519T>C
ENST00000680582.1:n.2192T>C
ENST00000680613.1:c.*723T>C	ENSP00000506114.1:n.*723T>C
ENST00000680662.1:c.*1144T>C	ENSP00000505080.1:n.*1144T>C
ENST00000680691.1:c.*893T>C	ENSP00000506487.1:n.*893T>C
ENST00000680694.1:c.*818T>C	ENSP00000505658.1:n.*818T>C
ENST00000680743.1:c.*1019T>C	ENSP00000505073.1:n.*1019T>C
ENST00000680749.1:c.*515T>C	ENSP00000505122.1:n.*515T>C
ENST00000680798.1:c.*2026T>C	ENSP00000505670.1:n.*2026T>C
ENST00000680805.1:c.1089T>C	ENSP00000505447.1:p.Ile363=
ENST00000680844.1:c.*2335T>C	ENSP00000506541.1:n.*2335T>C
ENST00000680948.1:c.*1097T>C	ENSP00000505441.1:n.*1097T>C
ENST00000680964.1:c.*1644T>C	ENSP00000505961.1:n.*1644T>C
ENST00000681037.1:c.*2714T>C	ENSP00000506025.1:n.*2714T>C
ENST00000681063.1:c.*499T>C	ENSP00000506616.1:n.*499T>C
ENST00000681209.1:c.*885T>C	ENSP00000505877.1:n.*885T>C
ENST00000681278.1:n.1932T>C
ENST00000681289.1:n.5225T>C
ENST00000681361.1:c.*2218T>C	ENSP00000506679.1:n.*2218T>C
ENST00000681430.1:c.*323T>C	ENSP00000506301.1:n.*323T>C
ENST00000681446.1:c.*2255T>C	ENSP00000506244.1:n.*2255T>C
ENST00000681450.1:c.*901T>C	ENSP00000505660.1:n.*901T>C
ENST00000681548.1:c.*2137T>C	ENSP00000505275.1:n.*2137T>C
ENST00000681616.1:c.*2210T>C	ENSP00000505111.1:n.*2210T>C
ENST00000681621.1:c.*2135T>C	ENSP00000505770.1:n.*2135T>C
ENST00000681680.1:n.4646T>C
ENST00000681720.1:c.*685T>C	ENSP00000505438.1:n.*685T>C
ENST00000681730.1:n.1452T>C
ENST00000681790.1:c.972T>C	ENSP00000505130.1:p.Ile324=
ENST00000681837.1:n.3167T>C
ENST00000681913.1:n.3476T>C
ENST00000681916.1:c.*998T>C	ENSP00000506477.1:n.*998T>C
ENST00000681930.1:n.4675T>C
ENST00000370834.9:c.1329T>C	ENSP00000359871.5:p.Ile443=
ENST00000370841.8:c.1230T>C	ENSP00000359878.4:p.Ile410=
ENST00000420607.6:c.1242T>C	ENSP00000409612.2:p.Ile414=
ENST00000481374.1:n.468-566T>C
ENST00000525808.5:c.*816T>C	ENSP00000434823.1:n.*816T>C
ENST00000526196.5:c.*998T>C	ENSP00000431953.1:n.*998T>C
ENST00000528016.1:c.160-6450T>C	ENSP00000434284.1:n.160-6450T>C
ENST00000529059.5:n.1139T>C
ENST00000541113.5:c.1122T>C	ENSP00000442324.1:p.Ile374=
NM_000016.5:c.1230T>C	NP_000007.1:p.Ile410=
NM_001127328.2:c.1242T>C	NP_001120800.1:p.Ile414=
NM_001286042.1:c.1122T>C	NP_001272971.1:p.Ile374=
NM_001286043.1:c.1329T>C	NP_001272972.1:p.Ile443=
NM_001286044.1:c.663T>C	NP_001272973.1:p.Ile221=
NM_000016.6:c.1230T>C MANE Select	NP_000007.1:p.Ile410=
NM_001127328.3:c.1242T>C	NP_001120800.1:p.Ile414=
NM_001286042.2:c.1122T>C	NP_001272971.1:p.Ile374=
NM_001286043.2:c.1329T>C	NP_001272972.1:p.Ile443=
NM_001286044.2:c.663T>C	NP_001272973.1:p.Ile221=