Canonical Allele Identifier: CA418545033

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76216183T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75750498T>C , CM000663.2:g.75750498T>C	GRCh38
NC_000001.10:g.76216183T>C , CM000663.1:g.76216183T>C	GRCh37
NC_000001.9:g.75988771T>C	NCBI36
NG_007045.2:g.31141T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.897T>C MANE Select	ENSP00000359878.5:p.Ala299=
ENST00000473018.3:n.3021T>C
ENST00000532207.6:n.1786T>C
ENST00000541113.6:c.849+939T>C	ENSP00000442324.2:n.849+939T>C
ENST00000679509.1:n.1859T>C
ENST00000679530.1:c.*665T>C	ENSP00000506454.1:n.*665T>C
ENST00000679615.1:n.2912T>C
ENST00000679687.1:c.459T>C	ENSP00000506598.1:p.Ala153=
ENST00000679704.1:c.*663T>C	ENSP00000505117.1:n.*663T>C
ENST00000679709.1:c.*860T>C	ENSP00000506623.1:n.*860T>C
ENST00000679976.1:c.*481T>C	ENSP00000505565.1:n.*481T>C
ENST00000680166.1:n.4186T>C
ENST00000680315.1:n.780T>C
ENST00000680517.1:c.*285T>C	ENSP00000505803.1:n.*285T>C
ENST00000680582.1:n.1859T>C
ENST00000680613.1:c.*268T>C	ENSP00000506114.1:n.*268T>C
ENST00000680662.1:c.*811T>C	ENSP00000505080.1:n.*811T>C
ENST00000680691.1:c.*560T>C	ENSP00000506487.1:n.*560T>C
ENST00000680694.1:c.*485T>C	ENSP00000505658.1:n.*485T>C
ENST00000680743.1:c.*564T>C	ENSP00000505073.1:n.*564T>C
ENST00000680749.1:c.*182T>C	ENSP00000505122.1:n.*182T>C
ENST00000680798.1:c.*372T>C	ENSP00000505670.1:n.*372T>C
ENST00000680805.1:c.756T>C	ENSP00000505447.1:p.Ala252=
ENST00000680844.1:c.*681T>C	ENSP00000506541.1:n.*681T>C
ENST00000680948.1:c.*764T>C	ENSP00000505441.1:n.*764T>C
ENST00000680964.1:c.897T>C	ENSP00000505961.1:p.Ala299=
ENST00000681037.1:c.*2381T>C	ENSP00000506025.1:n.*2381T>C
ENST00000681063.1:c.*44T>C	ENSP00000506616.1:n.*44T>C
ENST00000681209.1:c.*552T>C	ENSP00000505877.1:n.*552T>C
ENST00000681278.1:n.1254T>C
ENST00000681289.1:n.4892T>C
ENST00000681361.1:c.*564T>C	ENSP00000506679.1:n.*564T>C
ENST00000681430.1:c.897T>C	ENSP00000506301.1:p.Ala299=
ENST00000681446.1:c.*479T>C	ENSP00000506244.1:n.*479T>C
ENST00000681450.1:c.*568T>C	ENSP00000505660.1:n.*568T>C
ENST00000681548.1:c.*483T>C	ENSP00000505275.1:n.*483T>C
ENST00000681616.1:c.*556T>C	ENSP00000505111.1:n.*556T>C
ENST00000681621.1:c.*481T>C	ENSP00000505770.1:n.*481T>C
ENST00000681680.1:n.2992T>C
ENST00000681720.1:c.*352T>C	ENSP00000505438.1:n.*352T>C
ENST00000681730.1:n.1119T>C
ENST00000681790.1:c.639T>C	ENSP00000505130.1:p.Ala213=
ENST00000681837.1:n.1513T>C
ENST00000681913.1:n.3021T>C
ENST00000681916.1:c.*665T>C	ENSP00000506477.1:n.*665T>C
ENST00000681930.1:n.3021T>C
ENST00000370834.9:c.996T>C	ENSP00000359871.5:p.Ala332=
ENST00000370841.8:c.897T>C	ENSP00000359878.4:p.Ala299=
ENST00000420607.6:c.909T>C	ENSP00000409612.2:p.Ala303=
ENST00000481374.1:n.48T>C
ENST00000525808.5:c.*483T>C	ENSP00000434823.1:n.*483T>C
ENST00000526129.5:c.*681T>C	ENSP00000434092.1:n.*681T>C
ENST00000526196.5:c.*665T>C	ENSP00000431953.1:n.*665T>C
ENST00000528016.1:c.111T>C	ENSP00000434284.1:p.Ala37=
ENST00000529059.5:n.806T>C
ENST00000532207.5:n.627T>C
ENST00000534334.5:c.*481T>C	ENSP00000435584.1:n.*481T>C
ENST00000541113.5:c.789T>C	ENSP00000442324.1:p.Ala263=
NM_000016.5:c.897T>C	NP_000007.1:p.Ala299=
NM_001127328.2:c.909T>C	NP_001120800.1:p.Ala303=
NM_001286042.1:c.789T>C	NP_001272971.1:p.Ala263=
NM_001286043.1:c.996T>C	NP_001272972.1:p.Ala332=
NM_001286044.1:c.330T>C	NP_001272973.1:p.Ala110=
NM_000016.6:c.897T>C MANE Select	NP_000007.1:p.Ala299=
NM_001127328.3:c.909T>C	NP_001120800.1:p.Ala303=
NM_001286042.2:c.789T>C	NP_001272971.1:p.Ala263=
NM_001286043.2:c.996T>C	NP_001272972.1:p.Ala332=
NM_001286044.2:c.330T>C	NP_001272973.1:p.Ala110=