Canonical Allele Identifier: CA340818158

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226957A>T (hg19) ; chr1:g.75761272A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761272A>T , CM000663.2:g.75761272A>T	GRCh38
NC_000001.10:g.76226957A>T , CM000663.1:g.76226957A>T	GRCh37
NC_000001.9:g.75999545A>T	NCBI36
NG_007045.2:g.41915A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.1096A>T MANE Select	ENSP00000359878.5:p.Asn366Tyr
ENST00000473018.3:n.3220A>T
ENST00000532207.6:n.2107A>T
ENST00000541113.6:c.1000A>T	ENSP00000442324.2:p.Asn334Tyr
ENST00000679509.1:n.2058A>T
ENST00000679530.1:c.*864A>T	ENSP00000506454.1:n.*864A>T
ENST00000679615.1:n.3111A>T
ENST00000679687.1:c.658A>T	ENSP00000506598.1:p.Asn220Tyr
ENST00000679704.1:c.*862A>T	ENSP00000505117.1:n.*862A>T
ENST00000679709.1:c.*1059A>T	ENSP00000506623.1:n.*1059A>T
ENST00000679976.1:c.*680A>T	ENSP00000505565.1:n.*680A>T
ENST00000680166.1:n.4385A>T
ENST00000680315.1:n.979A>T
ENST00000680517.1:c.*484A>T	ENSP00000505803.1:n.*484A>T
ENST00000680582.1:n.2058A>T
ENST00000680613.1:c.*589A>T	ENSP00000506114.1:n.*589A>T
ENST00000680662.1:c.*1010A>T	ENSP00000505080.1:n.*1010A>T
ENST00000680691.1:c.*759A>T	ENSP00000506487.1:n.*759A>T
ENST00000680694.1:c.*684A>T	ENSP00000505658.1:n.*684A>T
ENST00000680743.1:c.*885A>T	ENSP00000505073.1:n.*885A>T
ENST00000680749.1:c.*381A>T	ENSP00000505122.1:n.*381A>T
ENST00000680798.1:c.*571A>T	ENSP00000505670.1:n.*571A>T
ENST00000680805.1:c.955A>T	ENSP00000505447.1:p.Asn319Tyr
ENST00000680844.1:c.*880A>T	ENSP00000506541.1:n.*880A>T
ENST00000680948.1:c.*963A>T	ENSP00000505441.1:n.*963A>T
ENST00000680964.1:c.*189A>T	ENSP00000505961.1:n.*189A>T
ENST00000681037.1:c.*2580A>T	ENSP00000506025.1:n.*2580A>T
ENST00000681063.1:c.*365A>T	ENSP00000506616.1:n.*365A>T
ENST00000681209.1:c.*751A>T	ENSP00000505877.1:n.*751A>T
ENST00000681278.1:n.1798A>T
ENST00000681289.1:n.5091A>T
ENST00000681361.1:c.*763A>T	ENSP00000506679.1:n.*763A>T
ENST00000681430.1:c.*189A>T	ENSP00000506301.1:n.*189A>T
ENST00000681446.1:c.*800A>T	ENSP00000506244.1:n.*800A>T
ENST00000681450.1:c.*767A>T	ENSP00000505660.1:n.*767A>T
ENST00000681548.1:c.*682A>T	ENSP00000505275.1:n.*682A>T
ENST00000681616.1:c.*755A>T	ENSP00000505111.1:n.*755A>T
ENST00000681621.1:c.*680A>T	ENSP00000505770.1:n.*680A>T
ENST00000681680.1:n.3191A>T
ENST00000681720.1:c.*551A>T	ENSP00000505438.1:n.*551A>T
ENST00000681730.1:n.1318A>T
ENST00000681790.1:c.838A>T	ENSP00000505130.1:p.Asn280Tyr
ENST00000681837.1:n.1712A>T
ENST00000681913.1:n.3342A>T
ENST00000681916.1:c.*864A>T	ENSP00000506477.1:n.*864A>T
ENST00000681930.1:n.3220A>T
ENST00000370834.9:c.1195A>T	ENSP00000359871.5:p.Asn399Tyr
ENST00000370841.8:c.1096A>T	ENSP00000359878.4:p.Asn366Tyr
ENST00000420607.6:c.1108A>T	ENSP00000409612.2:p.Asn370Tyr
ENST00000481374.1:n.369A>T
ENST00000525808.5:c.*682A>T	ENSP00000434823.1:n.*682A>T
ENST00000526129.5:c.*880A>T	ENSP00000434092.1:n.*880A>T
ENST00000526196.5:c.*864A>T	ENSP00000431953.1:n.*864A>T
ENST00000528016.1:c.160-7905A>T	ENSP00000434284.1:n.160-7905A>T
ENST00000529059.5:n.1005A>T
ENST00000541113.5:c.988A>T	ENSP00000442324.1:p.Asn330Tyr
NM_000016.5:c.1096A>T	NP_000007.1:p.Asn366Tyr
NM_001127328.2:c.1108A>T	NP_001120800.1:p.Asn370Tyr
NM_001286042.1:c.988A>T	NP_001272971.1:p.Asn330Tyr
NM_001286043.1:c.1195A>T	NP_001272972.1:p.Asn399Tyr
NM_001286044.1:c.529A>T	NP_001272973.1:p.Asn177Tyr
NM_000016.6:c.1096A>T MANE Select	NP_000007.1:p.Asn366Tyr
NM_001127328.3:c.1108A>T	NP_001120800.1:p.Asn370Tyr
NM_001286042.2:c.988A>T	NP_001272971.1:p.Asn330Tyr
NM_001286043.2:c.1195A>T	NP_001272972.1:p.Asn399Tyr
NM_001286044.2:c.529A>T	NP_001272973.1:p.Asn177Tyr