Canonical Allele Identifier: CA1324888883
Gene: ACADL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.210195338T= , CM000664.2:g.210195338T= GRCh38
NC_000002.11:g.211060062T= , CM000664.1:g.211060062T= GRCh37
NC_000002.10:g.210768307T= NCBI36
NG_008002.1:g.35154A=

Transcript Alleles

HGVS Amino-acid change
ENST00000233710.4:c.985A= MANE Select ENSP00000233710.3:p.Thr329=
ENST00000652584.1:n.1213A=
ENST00000233710.3:c.985A= ENSP00000233710.3:p.Thr329=
NM_001608.3:c.985A= NP_001599.1:p.Thr329=
XM_005246517.3:c.922A= XP_005246574.1:p.Thr308=
XM_005246517.4:c.922A= XP_005246574.1:p.Thr308=
XM_017003955.1:c.562A= XP_016859444.1:p.Thr188=
NM_001608.4:c.985A= MANE Select NP_001599.1:p.Thr329=