Canonical Allele Identifier: CA418544851

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76215169T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75749484T>C , CM000663.2:g.75749484T>C	GRCh38
NC_000001.10:g.76215169T>C , CM000663.1:g.76215169T>C	GRCh37
NC_000001.9:g.75987757T>C	NCBI36
NG_007045.2:g.30127T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370841.9:c.774T>C MANE Select	ENSP00000359878.5:p.Pro258=
ENST00000473018.3:n.2898T>C
ENST00000532207.6:n.1663T>C
ENST00000541113.6:c.774T>C	ENSP00000442324.2:p.Pro258=
ENST00000679509.1:n.1736T>C
ENST00000679530.1:c.*542T>C	ENSP00000506454.1:n.*542T>C
ENST00000679615.1:n.2789T>C
ENST00000679687.1:c.336T>C	ENSP00000506598.1:p.Pro112=
ENST00000679704.1:c.*540T>C	ENSP00000505117.1:n.*540T>C
ENST00000679709.1:c.*737T>C	ENSP00000506623.1:n.*737T>C
ENST00000679976.1:c.*358T>C	ENSP00000505565.1:n.*358T>C
ENST00000680166.1:n.4063T>C
ENST00000680517.1:c.*162T>C	ENSP00000505803.1:n.*162T>C
ENST00000680582.1:n.1736T>C
ENST00000680613.1:c.*145T>C	ENSP00000506114.1:n.*145T>C
ENST00000680662.1:c.*688T>C	ENSP00000505080.1:n.*688T>C
ENST00000680691.1:c.*437T>C	ENSP00000506487.1:n.*437T>C
ENST00000680694.1:c.*362T>C	ENSP00000505658.1:n.*362T>C
ENST00000680743.1:c.*441T>C	ENSP00000505073.1:n.*441T>C
ENST00000680749.1:c.*59T>C	ENSP00000505122.1:n.*59T>C
ENST00000680798.1:c.*249T>C	ENSP00000505670.1:n.*249T>C
ENST00000680805.1:c.709-967T>C	ENSP00000505447.1:n.709-967T>C
ENST00000680844.1:c.*558T>C	ENSP00000506541.1:n.*558T>C
ENST00000680948.1:c.*641T>C	ENSP00000505441.1:n.*641T>C
ENST00000680964.1:c.774T>C	ENSP00000505961.1:p.Pro258=
ENST00000681037.1:c.*2258T>C	ENSP00000506025.1:n.*2258T>C
ENST00000681063.1:c.600-967T>C	ENSP00000506616.1:n.600-967T>C
ENST00000681209.1:c.*429T>C	ENSP00000505877.1:n.*429T>C
ENST00000681278.1:n.1131T>C
ENST00000681289.1:n.4769T>C
ENST00000681361.1:c.*441T>C	ENSP00000506679.1:n.*441T>C
ENST00000681430.1:c.774T>C	ENSP00000506301.1:p.Pro258=
ENST00000681446.1:c.*356T>C	ENSP00000506244.1:n.*356T>C
ENST00000681450.1:c.*445T>C	ENSP00000505660.1:n.*445T>C
ENST00000681548.1:c.*360T>C	ENSP00000505275.1:n.*360T>C
ENST00000681616.1:c.*433T>C	ENSP00000505111.1:n.*433T>C
ENST00000681621.1:c.*358T>C	ENSP00000505770.1:n.*358T>C
ENST00000681680.1:n.2869T>C
ENST00000681720.1:c.*229T>C	ENSP00000505438.1:n.*229T>C
ENST00000681730.1:n.996T>C
ENST00000681790.1:c.516T>C	ENSP00000505130.1:p.Pro172=
ENST00000681837.1:n.1390T>C
ENST00000681913.1:n.2898T>C
ENST00000681916.1:c.*542T>C	ENSP00000506477.1:n.*542T>C
ENST00000681930.1:n.2898T>C
ENST00000370834.9:c.873T>C	ENSP00000359871.5:p.Pro291=
ENST00000370841.8:c.774T>C	ENSP00000359878.4:p.Pro258=
ENST00000420607.6:c.786T>C	ENSP00000409612.2:p.Pro262=
ENST00000525808.5:c.*360T>C	ENSP00000434823.1:n.*360T>C
ENST00000526129.5:c.*558T>C	ENSP00000434092.1:n.*558T>C
ENST00000526196.5:c.*542T>C	ENSP00000431953.1:n.*542T>C
ENST00000526930.1:n.547T>C
ENST00000529059.5:n.683T>C
ENST00000530953.6:c.*271T>C	ENSP00000431372.1:n.*271T>C
ENST00000532207.5:n.504T>C
ENST00000532509.5:c.*538T>C	ENSP00000432522.1:n.*538T>C
ENST00000534334.5:c.*358T>C	ENSP00000435584.1:n.*358T>C
ENST00000541113.5:c.666T>C	ENSP00000442324.1:p.Pro222=
NM_000016.5:c.774T>C	NP_000007.1:p.Pro258=
NM_001127328.2:c.786T>C	NP_001120800.1:p.Pro262=
NM_001286042.1:c.666T>C	NP_001272971.1:p.Pro222=
NM_001286043.1:c.873T>C	NP_001272972.1:p.Pro291=
NM_001286044.1:c.207T>C	NP_001272973.1:p.Pro69=
NM_000016.6:c.774T>C MANE Select	NP_000007.1:p.Pro258=
NM_001127328.3:c.786T>C	NP_001120800.1:p.Pro262=
NM_001286042.2:c.666T>C	NP_001272971.1:p.Pro222=
NM_001286043.2:c.873T>C	NP_001272972.1:p.Pro291=
NM_001286044.2:c.207T>C	NP_001272973.1:p.Pro69=