Canonical Allele Identifier: CA2646245811
Gene: ACADM HGNC NCBI

Linked Data

gnomAD v4: 1-75724693-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75724693T>C , CM000663.2:g.75724693T>C GRCh38
NC_000001.10:g.76190378T>C , CM000663.1:g.76190378T>C GRCh37
NC_000001.9:g.75962966T>C NCBI36
NG_007045.2:g.5336T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000473018.3:n.263T>C
ENST00000525881.6:n.263T>C
ENST00000541113.6:c.-95T>C ENSP00000442324.2:n.-95T>C
ENST00000679509.1:n.263T>C
ENST00000679530.1:c.-95T>C ENSP00000506454.1:n.-95T>C
ENST00000679615.1:n.263T>C
ENST00000679976.1:c.-95T>C ENSP00000505565.1:n.-95T>C
ENST00000680517.1:c.-95T>C ENSP00000505803.1:n.-95T>C
ENST00000680582.1:n.263T>C
ENST00000680613.1:c.-95T>C ENSP00000506114.1:n.-95T>C
ENST00000680691.1:c.-95T>C ENSP00000506487.1:n.-95T>C
ENST00000680694.1:c.-95T>C ENSP00000505658.1:n.-95T>C
ENST00000680749.1:c.-95T>C ENSP00000505122.1:n.-95T>C
ENST00000680798.1:c.-95T>C ENSP00000505670.1:n.-95T>C
ENST00000680805.1:c.-95T>C ENSP00000505447.1:n.-95T>C
ENST00000680964.1:c.-95T>C ENSP00000505961.1:n.-95T>C
ENST00000681037.1:c.-95T>C ENSP00000506025.1:n.-95T>C
ENST00000681063.1:c.-95T>C ENSP00000506616.1:n.-95T>C
ENST00000681209.1:c.-95T>C ENSP00000505877.1:n.-95T>C
ENST00000681278.1:n.263T>C
ENST00000681289.1:n.263T>C
ENST00000681361.1:c.-95T>C ENSP00000506679.1:n.-95T>C
ENST00000681430.1:c.-95T>C ENSP00000506301.1:n.-95T>C
ENST00000681446.1:c.-95T>C ENSP00000506244.1:n.-95T>C
ENST00000681621.1:c.-95T>C ENSP00000505770.1:n.-95T>C
ENST00000681680.1:n.263T>C
ENST00000681790.1:c.-374T>C ENSP00000505130.1:n.-374T>C
ENST00000681837.1:n.5T>C
ENST00000681913.1:n.263T>C
ENST00000681930.1:n.263T>C
ENST00000370841.8:c.-95T>C ENSP00000359878.4:n.-95T>C
ENST00000525881.5:n.3T>C
ENST00000541113.5:c.-115T>C ENSP00000442324.1:n.-115T>C
NM_000016.5:c.-95T>C NP_000007.1:n.-95T>C
NM_001127328.2:c.-95T>C NP_001120800.1:n.-95T>C
NM_001286042.1:c.-115T>C NP_001272971.1:n.-115T>C
NM_001286043.1:c.-95T>C NP_001272972.1:n.-95T>C
NM_001286044.1:c.-392T>C NP_001272973.1:n.-392T>C