Canonical Allele Identifier: CA340817980

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76226871A>T (hg19) ; chr1:g.75761186A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75761186A>T , CM000663.2:g.75761186A>T	GRCh38
NC_000001.10:g.76226871A>T , CM000663.1:g.76226871A>T	GRCh37
NC_000001.9:g.75999459A>T	NCBI36
NG_007045.2:g.41829A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.1010A>T MANE Select	ENSP00000359878.5:p.Tyr337Phe
ENST00000473018.3:n.3134A>T
ENST00000532207.6:n.2021A>T
ENST00000541113.6:c.914A>T	ENSP00000442324.2:p.Tyr305Phe
ENST00000679509.1:n.1972A>T
ENST00000679530.1:c.*778A>T	ENSP00000506454.1:n.*778A>T
ENST00000679615.1:n.3025A>T
ENST00000679687.1:c.572A>T	ENSP00000506598.1:p.Tyr191Phe
ENST00000679704.1:c.*776A>T	ENSP00000505117.1:n.*776A>T
ENST00000679709.1:c.*973A>T	ENSP00000506623.1:n.*973A>T
ENST00000679976.1:c.*594A>T	ENSP00000505565.1:n.*594A>T
ENST00000680166.1:n.4299A>T
ENST00000680315.1:n.893A>T
ENST00000680517.1:c.*398A>T	ENSP00000505803.1:n.*398A>T
ENST00000680582.1:n.1972A>T
ENST00000680613.1:c.*503A>T	ENSP00000506114.1:n.*503A>T
ENST00000680662.1:c.*924A>T	ENSP00000505080.1:n.*924A>T
ENST00000680691.1:c.*673A>T	ENSP00000506487.1:n.*673A>T
ENST00000680694.1:c.*598A>T	ENSP00000505658.1:n.*598A>T
ENST00000680743.1:c.*799A>T	ENSP00000505073.1:n.*799A>T
ENST00000680749.1:c.*295A>T	ENSP00000505122.1:n.*295A>T
ENST00000680798.1:c.*485A>T	ENSP00000505670.1:n.*485A>T
ENST00000680805.1:c.869A>T	ENSP00000505447.1:p.Tyr290Phe
ENST00000680844.1:c.*794A>T	ENSP00000506541.1:n.*794A>T
ENST00000680948.1:c.*877A>T	ENSP00000505441.1:n.*877A>T
ENST00000680964.1:c.*103A>T	ENSP00000505961.1:n.*103A>T
ENST00000681037.1:c.*2494A>T	ENSP00000506025.1:n.*2494A>T
ENST00000681063.1:c.*279A>T	ENSP00000506616.1:n.*279A>T
ENST00000681209.1:c.*665A>T	ENSP00000505877.1:n.*665A>T
ENST00000681278.1:n.1712A>T
ENST00000681289.1:n.5005A>T
ENST00000681361.1:c.*677A>T	ENSP00000506679.1:n.*677A>T
ENST00000681430.1:c.*103A>T	ENSP00000506301.1:n.*103A>T
ENST00000681446.1:c.*714A>T	ENSP00000506244.1:n.*714A>T
ENST00000681450.1:c.*681A>T	ENSP00000505660.1:n.*681A>T
ENST00000681548.1:c.*596A>T	ENSP00000505275.1:n.*596A>T
ENST00000681616.1:c.*669A>T	ENSP00000505111.1:n.*669A>T
ENST00000681621.1:c.*594A>T	ENSP00000505770.1:n.*594A>T
ENST00000681680.1:n.3105A>T
ENST00000681720.1:c.*465A>T	ENSP00000505438.1:n.*465A>T
ENST00000681730.1:n.1232A>T
ENST00000681790.1:c.752A>T	ENSP00000505130.1:p.Tyr251Phe
ENST00000681837.1:n.1626A>T
ENST00000681913.1:n.3256A>T
ENST00000681916.1:c.*778A>T	ENSP00000506477.1:n.*778A>T
ENST00000681930.1:n.3134A>T
ENST00000370834.9:c.1109A>T	ENSP00000359871.5:p.Tyr370Phe
ENST00000370841.8:c.1010A>T	ENSP00000359878.4:p.Tyr337Phe
ENST00000420607.6:c.1022A>T	ENSP00000409612.2:p.Tyr341Phe
ENST00000481374.1:n.283A>T
ENST00000525808.5:c.*596A>T	ENSP00000434823.1:n.*596A>T
ENST00000526129.5:c.*794A>T	ENSP00000434092.1:n.*794A>T
ENST00000526196.5:c.*778A>T	ENSP00000431953.1:n.*778A>T
ENST00000528016.1:c.160-7991A>T	ENSP00000434284.1:n.160-7991A>T
ENST00000529059.5:n.919A>T
ENST00000532207.5:n.740A>T
ENST00000534334.5:c.*751A>T	ENSP00000435584.1:n.*751A>T
ENST00000541113.5:c.902A>T	ENSP00000442324.1:p.Tyr301Phe
NM_000016.5:c.1010A>T	NP_000007.1:p.Tyr337Phe
NM_001127328.2:c.1022A>T	NP_001120800.1:p.Tyr341Phe
NM_001286042.1:c.902A>T	NP_001272971.1:p.Tyr301Phe
NM_001286043.1:c.1109A>T	NP_001272972.1:p.Tyr370Phe
NM_001286044.1:c.443A>T	NP_001272973.1:p.Tyr148Phe
NM_000016.6:c.1010A>T MANE Select	NP_000007.1:p.Tyr337Phe
NM_001127328.3:c.1022A>T	NP_001120800.1:p.Tyr341Phe
NM_001286042.2:c.902A>T	NP_001272971.1:p.Tyr301Phe
NM_001286043.2:c.1109A>T	NP_001272972.1:p.Tyr370Phe
NM_001286044.2:c.443A>T	NP_001272973.1:p.Tyr148Phe