Canonical Allele Identifier: CA340816661

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76215177A>T (hg19) ; chr1:g.75749492A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75749492A>T , CM000663.2:g.75749492A>T	GRCh38
NC_000001.10:g.76215177A>T , CM000663.1:g.76215177A>T	GRCh37
NC_000001.9:g.75987765A>T	NCBI36
NG_007045.2:g.30135A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.782A>T MANE Select	ENSP00000359878.5:p.Asn261Ile
ENST00000473018.3:n.2906A>T
ENST00000532207.6:n.1671A>T
ENST00000541113.6:c.782A>T	ENSP00000442324.2:p.Asn261Ile
ENST00000679509.1:n.1744A>T
ENST00000679530.1:c.*550A>T	ENSP00000506454.1:n.*550A>T
ENST00000679615.1:n.2797A>T
ENST00000679687.1:c.344A>T	ENSP00000506598.1:p.Asn115Ile
ENST00000679704.1:c.*548A>T	ENSP00000505117.1:n.*548A>T
ENST00000679709.1:c.*745A>T	ENSP00000506623.1:n.*745A>T
ENST00000679976.1:c.*366A>T	ENSP00000505565.1:n.*366A>T
ENST00000680166.1:n.4071A>T
ENST00000680517.1:c.*170A>T	ENSP00000505803.1:n.*170A>T
ENST00000680582.1:n.1744A>T
ENST00000680613.1:c.*153A>T	ENSP00000506114.1:n.*153A>T
ENST00000680662.1:c.*696A>T	ENSP00000505080.1:n.*696A>T
ENST00000680691.1:c.*445A>T	ENSP00000506487.1:n.*445A>T
ENST00000680694.1:c.*370A>T	ENSP00000505658.1:n.*370A>T
ENST00000680743.1:c.*449A>T	ENSP00000505073.1:n.*449A>T
ENST00000680749.1:c.*67A>T	ENSP00000505122.1:n.*67A>T
ENST00000680798.1:c.*257A>T	ENSP00000505670.1:n.*257A>T
ENST00000680805.1:c.709-959A>T	ENSP00000505447.1:n.709-959A>T
ENST00000680844.1:c.*566A>T	ENSP00000506541.1:n.*566A>T
ENST00000680948.1:c.*649A>T	ENSP00000505441.1:n.*649A>T
ENST00000680964.1:c.782A>T	ENSP00000505961.1:p.Asn261Ile
ENST00000681037.1:c.*2266A>T	ENSP00000506025.1:n.*2266A>T
ENST00000681063.1:c.600-959A>T	ENSP00000506616.1:n.600-959A>T
ENST00000681209.1:c.*437A>T	ENSP00000505877.1:n.*437A>T
ENST00000681278.1:n.1139A>T
ENST00000681289.1:n.4777A>T
ENST00000681361.1:c.*449A>T	ENSP00000506679.1:n.*449A>T
ENST00000681430.1:c.782A>T	ENSP00000506301.1:p.Asn261Ile
ENST00000681446.1:c.*364A>T	ENSP00000506244.1:n.*364A>T
ENST00000681450.1:c.*453A>T	ENSP00000505660.1:n.*453A>T
ENST00000681548.1:c.*368A>T	ENSP00000505275.1:n.*368A>T
ENST00000681616.1:c.*441A>T	ENSP00000505111.1:n.*441A>T
ENST00000681621.1:c.*366A>T	ENSP00000505770.1:n.*366A>T
ENST00000681680.1:n.2877A>T
ENST00000681720.1:c.*237A>T	ENSP00000505438.1:n.*237A>T
ENST00000681730.1:n.1004A>T
ENST00000681790.1:c.524A>T	ENSP00000505130.1:p.Asn175Ile
ENST00000681837.1:n.1398A>T
ENST00000681913.1:n.2906A>T
ENST00000681916.1:c.*550A>T	ENSP00000506477.1:n.*550A>T
ENST00000681930.1:n.2906A>T
ENST00000370834.9:c.881A>T	ENSP00000359871.5:p.Asn294Ile
ENST00000370841.8:c.782A>T	ENSP00000359878.4:p.Asn261Ile
ENST00000420607.6:c.794A>T	ENSP00000409612.2:p.Asn265Ile
ENST00000525808.5:c.*368A>T	ENSP00000434823.1:n.*368A>T
ENST00000526129.5:c.*566A>T	ENSP00000434092.1:n.*566A>T
ENST00000526196.5:c.*550A>T	ENSP00000431953.1:n.*550A>T
ENST00000526930.1:n.555A>T
ENST00000529059.5:n.691A>T
ENST00000530953.6:c.*279A>T	ENSP00000431372.1:n.*279A>T
ENST00000532207.5:n.512A>T
ENST00000532509.5:c.*546A>T	ENSP00000432522.1:n.*546A>T
ENST00000534334.5:c.*366A>T	ENSP00000435584.1:n.*366A>T
ENST00000541113.5:c.674A>T	ENSP00000442324.1:p.Asn225Ile
NM_000016.5:c.782A>T	NP_000007.1:p.Asn261Ile
NM_001127328.2:c.794A>T	NP_001120800.1:p.Asn265Ile
NM_001286042.1:c.674A>T	NP_001272971.1:p.Asn225Ile
NM_001286043.1:c.881A>T	NP_001272972.1:p.Asn294Ile
NM_001286044.1:c.215A>T	NP_001272973.1:p.Asn72Ile
NM_000016.6:c.782A>T MANE Select	NP_000007.1:p.Asn261Ile
NM_001127328.3:c.794A>T	NP_001120800.1:p.Asn265Ile
NM_001286042.2:c.674A>T	NP_001272971.1:p.Asn225Ile
NM_001286043.2:c.881A>T	NP_001272972.1:p.Asn294Ile
NM_001286044.2:c.215A>T	NP_001272973.1:p.Asn72Ile