Canonical Allele Identifier: CA340817095

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76216190T>G (hg19) ; chr1:g.75750505T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75750505T>G , CM000663.2:g.75750505T>G	GRCh38
NC_000001.10:g.76216190T>G , CM000663.1:g.76216190T>G	GRCh37
NC_000001.9:g.75988778T>G	NCBI36
NG_007045.2:g.31148T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.904T>G MANE Select	ENSP00000359878.5:p.Tyr302Asp
ENST00000473018.3:n.3028T>G
ENST00000532207.6:n.1793T>G
ENST00000541113.6:c.849+946T>G	ENSP00000442324.2:n.849+946T>G
ENST00000679509.1:n.1866T>G
ENST00000679530.1:c.*672T>G	ENSP00000506454.1:n.*672T>G
ENST00000679615.1:n.2919T>G
ENST00000679687.1:c.466T>G	ENSP00000506598.1:p.Tyr156Asp
ENST00000679704.1:c.*670T>G	ENSP00000505117.1:n.*670T>G
ENST00000679709.1:c.*867T>G	ENSP00000506623.1:n.*867T>G
ENST00000679976.1:c.*488T>G	ENSP00000505565.1:n.*488T>G
ENST00000680166.1:n.4193T>G
ENST00000680315.1:n.787T>G
ENST00000680517.1:c.*292T>G	ENSP00000505803.1:n.*292T>G
ENST00000680582.1:n.1866T>G
ENST00000680613.1:c.*275T>G	ENSP00000506114.1:n.*275T>G
ENST00000680662.1:c.*818T>G	ENSP00000505080.1:n.*818T>G
ENST00000680691.1:c.*567T>G	ENSP00000506487.1:n.*567T>G
ENST00000680694.1:c.*492T>G	ENSP00000505658.1:n.*492T>G
ENST00000680743.1:c.*571T>G	ENSP00000505073.1:n.*571T>G
ENST00000680749.1:c.*189T>G	ENSP00000505122.1:n.*189T>G
ENST00000680798.1:c.*379T>G	ENSP00000505670.1:n.*379T>G
ENST00000680805.1:c.763T>G	ENSP00000505447.1:p.Tyr255Asp
ENST00000680844.1:c.*688T>G	ENSP00000506541.1:n.*688T>G
ENST00000680948.1:c.*771T>G	ENSP00000505441.1:n.*771T>G
ENST00000680964.1:c.904T>G	ENSP00000505961.1:p.Tyr302Asp
ENST00000681037.1:c.*2388T>G	ENSP00000506025.1:n.*2388T>G
ENST00000681063.1:c.*51T>G	ENSP00000506616.1:n.*51T>G
ENST00000681209.1:c.*559T>G	ENSP00000505877.1:n.*559T>G
ENST00000681278.1:n.1261T>G
ENST00000681289.1:n.4899T>G
ENST00000681361.1:c.*571T>G	ENSP00000506679.1:n.*571T>G
ENST00000681430.1:c.904T>G	ENSP00000506301.1:p.Tyr302Asp
ENST00000681446.1:c.*486T>G	ENSP00000506244.1:n.*486T>G
ENST00000681450.1:c.*575T>G	ENSP00000505660.1:n.*575T>G
ENST00000681548.1:c.*490T>G	ENSP00000505275.1:n.*490T>G
ENST00000681616.1:c.*563T>G	ENSP00000505111.1:n.*563T>G
ENST00000681621.1:c.*488T>G	ENSP00000505770.1:n.*488T>G
ENST00000681680.1:n.2999T>G
ENST00000681720.1:c.*359T>G	ENSP00000505438.1:n.*359T>G
ENST00000681730.1:n.1126T>G
ENST00000681790.1:c.646T>G	ENSP00000505130.1:p.Tyr216Asp
ENST00000681837.1:n.1520T>G
ENST00000681913.1:n.3028T>G
ENST00000681916.1:c.*672T>G	ENSP00000506477.1:n.*672T>G
ENST00000681930.1:n.3028T>G
ENST00000370834.9:c.1003T>G	ENSP00000359871.5:p.Tyr335Asp
ENST00000370841.8:c.904T>G	ENSP00000359878.4:p.Tyr302Asp
ENST00000420607.6:c.916T>G	ENSP00000409612.2:p.Tyr306Asp
ENST00000481374.1:n.55T>G
ENST00000525808.5:c.*490T>G	ENSP00000434823.1:n.*490T>G
ENST00000526129.5:c.*688T>G	ENSP00000434092.1:n.*688T>G
ENST00000526196.5:c.*672T>G	ENSP00000431953.1:n.*672T>G
ENST00000528016.1:c.118T>G	ENSP00000434284.1:p.Tyr40Asp
ENST00000529059.5:n.813T>G
ENST00000532207.5:n.634T>G
ENST00000534334.5:c.*488T>G	ENSP00000435584.1:n.*488T>G
ENST00000541113.5:c.796T>G	ENSP00000442324.1:p.Tyr266Asp
NM_000016.5:c.904T>G	NP_000007.1:p.Tyr302Asp
NM_001127328.2:c.916T>G	NP_001120800.1:p.Tyr306Asp
NM_001286042.1:c.796T>G	NP_001272971.1:p.Tyr266Asp
NM_001286043.1:c.1003T>G	NP_001272972.1:p.Tyr335Asp
NM_001286044.1:c.337T>G	NP_001272973.1:p.Tyr113Asp
NM_000016.6:c.904T>G MANE Select	NP_000007.1:p.Tyr302Asp
NM_001127328.3:c.916T>G	NP_001120800.1:p.Tyr306Asp
NM_001286042.2:c.796T>G	NP_001272971.1:p.Tyr266Asp
NM_001286043.2:c.1003T>G	NP_001272972.1:p.Tyr335Asp
NM_001286044.2:c.337T>G	NP_001272973.1:p.Tyr113Asp