Canonical Allele Identifier: CA340815376

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76205766G>T (hg19) ; chr1:g.75740081G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75740081G>T , CM000663.2:g.75740081G>T	GRCh38
NC_000001.10:g.76205766G>T , CM000663.1:g.76205766G>T	GRCh37
NC_000001.9:g.75978354G>T	NCBI36
NG_007045.2:g.20724G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.570G>T MANE Select	ENSP00000359878.5:p.Met190Ile
ENST00000473018.3:n.2694G>T
ENST00000541113.6:c.570G>T	ENSP00000442324.2:p.Met190Ile
ENST00000679509.1:n.1532G>T
ENST00000679530.1:c.*338G>T	ENSP00000506454.1:n.*338G>T
ENST00000679615.1:n.2694G>T
ENST00000679687.1:c.132G>T	ENSP00000506598.1:p.Met44Ile
ENST00000679704.1:c.*336G>T	ENSP00000505117.1:n.*336G>T
ENST00000679709.1:c.*533G>T	ENSP00000506623.1:n.*533G>T
ENST00000679804.1:n.309G>T
ENST00000679976.1:c.*154G>T	ENSP00000505565.1:n.*154G>T
ENST00000680166.1:n.3859G>T
ENST00000680517.1:c.*67G>T	ENSP00000505803.1:n.*67G>T
ENST00000680582.1:n.1532G>T
ENST00000680613.1:c.570G>T	ENSP00000506114.1:p.Met190Ile
ENST00000680662.1:c.*484G>T	ENSP00000505080.1:n.*484G>T
ENST00000680691.1:c.*233G>T	ENSP00000506487.1:n.*233G>T
ENST00000680694.1:c.*158G>T	ENSP00000505658.1:n.*158G>T
ENST00000680743.1:c.*237G>T	ENSP00000505073.1:n.*237G>T
ENST00000680749.1:c.570G>T	ENSP00000505122.1:p.Met190Ile
ENST00000680798.1:c.*154G>T	ENSP00000505670.1:n.*154G>T
ENST00000680805.1:c.570G>T	ENSP00000505447.1:p.Met190Ile
ENST00000680844.1:c.*354G>T	ENSP00000506541.1:n.*354G>T
ENST00000680948.1:c.*437G>T	ENSP00000505441.1:n.*437G>T
ENST00000680964.1:c.570G>T	ENSP00000505961.1:p.Met190Ile
ENST00000681037.1:c.570G>T	ENSP00000506025.1:p.Met190Ile
ENST00000681063.1:c.570G>T	ENSP00000506616.1:p.Met190Ile
ENST00000681209.1:c.*334G>T	ENSP00000505877.1:n.*334G>T
ENST00000681278.1:n.927G>T
ENST00000681289.1:n.927G>T
ENST00000681361.1:c.*237G>T	ENSP00000506679.1:n.*237G>T
ENST00000681430.1:c.570G>T	ENSP00000506301.1:p.Met190Ile
ENST00000681446.1:c.*152G>T	ENSP00000506244.1:n.*152G>T
ENST00000681450.1:c.*241G>T	ENSP00000505660.1:n.*241G>T
ENST00000681548.1:c.*156G>T	ENSP00000505275.1:n.*156G>T
ENST00000681616.1:c.*338G>T	ENSP00000505111.1:n.*338G>T
ENST00000681621.1:c.*154G>T	ENSP00000505770.1:n.*154G>T
ENST00000681680.1:n.2694G>T
ENST00000681720.1:c.*55-5725G>T	ENSP00000505438.1:n.*55-5725G>T
ENST00000681730.1:n.792G>T
ENST00000681790.1:c.312G>T	ENSP00000505130.1:p.Met104Ile
ENST00000681837.1:n.1186G>T
ENST00000681913.1:n.2694G>T
ENST00000681916.1:c.*338G>T	ENSP00000506477.1:n.*338G>T
ENST00000681930.1:n.2694G>T
ENST00000370834.9:c.669G>T	ENSP00000359871.5:p.Met223Ile
ENST00000370841.8:c.570G>T	ENSP00000359878.4:p.Met190Ile
ENST00000420607.6:c.582G>T	ENSP00000409612.2:p.Met194Ile
ENST00000525808.5:c.*156G>T	ENSP00000434823.1:n.*156G>T
ENST00000526129.5:c.*354G>T	ENSP00000434092.1:n.*354G>T
ENST00000526196.5:c.*338G>T	ENSP00000431953.1:n.*338G>T
ENST00000526930.1:n.343G>T
ENST00000529059.5:n.479G>T
ENST00000530953.6:c.*67G>T	ENSP00000431372.1:n.*67G>T
ENST00000532509.5:c.*334G>T	ENSP00000432522.1:n.*334G>T
ENST00000534334.5:c.*154G>T	ENSP00000435584.1:n.*154G>T
ENST00000541113.5:c.462G>T	ENSP00000442324.1:p.Met154Ile
NM_000016.5:c.570G>T	NP_000007.1:p.Met190Ile
NM_001127328.2:c.582G>T	NP_001120800.1:p.Met194Ile
NM_001286042.1:c.462G>T	NP_001272971.1:p.Met154Ile
NM_001286043.1:c.669G>T	NP_001272972.1:p.Met223Ile
NM_001286044.1:c.3G>T	NP_001272973.1:p.Met1Ile
NM_000016.6:c.570G>T MANE Select	NP_000007.1:p.Met190Ile
NM_001127328.3:c.582G>T	NP_001120800.1:p.Met194Ile
NM_001286042.2:c.462G>T	NP_001272971.1:p.Met154Ile
NM_001286043.2:c.669G>T	NP_001272972.1:p.Met223Ile
NM_001286044.2:c.3G>T	NP_001272973.1:p.Met1Ile