Canonical Allele Identifier: CA350418526
Gene: ACADL HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.211059951A>G (hg19) chr2:g.210195227A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.210195227A>G , CM000664.2:g.210195227A>G GRCh38
NC_000002.11:g.211059951A>G , CM000664.1:g.211059951A>G GRCh37
NC_000002.10:g.210768196A>G NCBI36
NG_008002.1:g.35265T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000233710.4:c.1096T>C MANE Select ENSP00000233710.3:p.Cys366Arg
ENST00000652584.1:n.1324T>C
ENST00000233710.3:c.1096T>C ENSP00000233710.3:p.Cys366Arg
NM_001608.3:c.1096T>C NP_001599.1:p.Cys366Arg
XM_005246517.3:c.1033T>C XP_005246574.1:p.Cys345Arg
XM_005246517.4:c.1033T>C XP_005246574.1:p.Cys345Arg
XM_017003955.1:c.673T>C XP_016859444.1:p.Cys225Arg
NM_001608.4:c.1096T>C MANE Select NP_001599.1:p.Cys366Arg
Search 100 bp 5'
Search 100 bp 3'