Canonical Allele Identifier: CA418707556

Gene: ACADM

Linked Data

• gnomAD v4: 1-75761199-T-A
• MyVariant Identifiers: chr1:g.76226884T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761199T>A , CM000663.2:g.75761199T>A	GRCh38
NC_000001.10:g.76226884T>A , CM000663.1:g.76226884T>A	GRCh37
NC_000001.9:g.75999472T>A	NCBI36
NG_007045.2:g.41842T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.1023T>A MANE Select	ENSP00000359878.5:p.Ala341=
ENST00000473018.3:n.3147T>A
ENST00000532207.6:n.2034T>A
ENST00000541113.6:c.927T>A	ENSP00000442324.2:p.Ala309=
ENST00000679509.1:n.1985T>A
ENST00000679530.1:c.*791T>A	ENSP00000506454.1:n.*791T>A
ENST00000679615.1:n.3038T>A
ENST00000679687.1:c.585T>A	ENSP00000506598.1:p.Ala195=
ENST00000679704.1:c.*789T>A	ENSP00000505117.1:n.*789T>A
ENST00000679709.1:c.*986T>A	ENSP00000506623.1:n.*986T>A
ENST00000679976.1:c.*607T>A	ENSP00000505565.1:n.*607T>A
ENST00000680166.1:n.4312T>A
ENST00000680315.1:n.906T>A
ENST00000680517.1:c.*411T>A	ENSP00000505803.1:n.*411T>A
ENST00000680582.1:n.1985T>A
ENST00000680613.1:c.*516T>A	ENSP00000506114.1:n.*516T>A
ENST00000680662.1:c.*937T>A	ENSP00000505080.1:n.*937T>A
ENST00000680691.1:c.*686T>A	ENSP00000506487.1:n.*686T>A
ENST00000680694.1:c.*611T>A	ENSP00000505658.1:n.*611T>A
ENST00000680743.1:c.*812T>A	ENSP00000505073.1:n.*812T>A
ENST00000680749.1:c.*308T>A	ENSP00000505122.1:n.*308T>A
ENST00000680798.1:c.*498T>A	ENSP00000505670.1:n.*498T>A
ENST00000680805.1:c.882T>A	ENSP00000505447.1:p.Ala294=
ENST00000680844.1:c.*807T>A	ENSP00000506541.1:n.*807T>A
ENST00000680948.1:c.*890T>A	ENSP00000505441.1:n.*890T>A
ENST00000680964.1:c.*116T>A	ENSP00000505961.1:n.*116T>A
ENST00000681037.1:c.*2507T>A	ENSP00000506025.1:n.*2507T>A
ENST00000681063.1:c.*292T>A	ENSP00000506616.1:n.*292T>A
ENST00000681209.1:c.*678T>A	ENSP00000505877.1:n.*678T>A
ENST00000681278.1:n.1725T>A
ENST00000681289.1:n.5018T>A
ENST00000681361.1:c.*690T>A	ENSP00000506679.1:n.*690T>A
ENST00000681430.1:c.*116T>A	ENSP00000506301.1:n.*116T>A
ENST00000681446.1:c.*727T>A	ENSP00000506244.1:n.*727T>A
ENST00000681450.1:c.*694T>A	ENSP00000505660.1:n.*694T>A
ENST00000681548.1:c.*609T>A	ENSP00000505275.1:n.*609T>A
ENST00000681616.1:c.*682T>A	ENSP00000505111.1:n.*682T>A
ENST00000681621.1:c.*607T>A	ENSP00000505770.1:n.*607T>A
ENST00000681680.1:n.3118T>A
ENST00000681720.1:c.*478T>A	ENSP00000505438.1:n.*478T>A
ENST00000681730.1:n.1245T>A
ENST00000681790.1:c.765T>A	ENSP00000505130.1:p.Ala255=
ENST00000681837.1:n.1639T>A
ENST00000681913.1:n.3269T>A
ENST00000681916.1:c.*791T>A	ENSP00000506477.1:n.*791T>A
ENST00000681930.1:n.3147T>A
ENST00000370834.9:c.1122T>A	ENSP00000359871.5:p.Ala374=
ENST00000370841.8:c.1023T>A	ENSP00000359878.4:p.Ala341=
ENST00000420607.6:c.1035T>A	ENSP00000409612.2:p.Ala345=
ENST00000481374.1:n.296T>A
ENST00000525808.5:c.*609T>A	ENSP00000434823.1:n.*609T>A
ENST00000526129.5:c.*807T>A	ENSP00000434092.1:n.*807T>A
ENST00000526196.5:c.*791T>A	ENSP00000431953.1:n.*791T>A
ENST00000528016.1:c.160-7978T>A	ENSP00000434284.1:n.160-7978T>A
ENST00000529059.5:n.932T>A
ENST00000532207.5:n.753T>A
ENST00000534334.5:c.*764T>A	ENSP00000435584.1:n.*764T>A
ENST00000541113.5:c.915T>A	ENSP00000442324.1:p.Ala305=
NM_000016.5:c.1023T>A	NP_000007.1:p.Ala341=
NM_001127328.2:c.1035T>A	NP_001120800.1:p.Ala345=
NM_001286042.1:c.915T>A	NP_001272971.1:p.Ala305=
NM_001286043.1:c.1122T>A	NP_001272972.1:p.Ala374=
NM_001286044.1:c.456T>A	NP_001272973.1:p.Ala152=
NM_000016.6:c.1023T>A MANE Select	NP_000007.1:p.Ala341=
NM_001127328.3:c.1035T>A	NP_001120800.1:p.Ala345=
NM_001286042.2:c.915T>A	NP_001272971.1:p.Ala305=
NM_001286043.2:c.1122T>A	NP_001272972.1:p.Ala374=
NM_001286044.2:c.456T>A	NP_001272973.1:p.Ala152=