Canonical Allele Identifier: CA1324888880
Gene: ACADL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.210195330T= , CM000664.2:g.210195330T= GRCh38
NC_000002.11:g.211060054T= , CM000664.1:g.211060054T= GRCh37
NC_000002.10:g.210768299T= NCBI36
NG_008002.1:g.35162A=

Transcript Alleles

HGVS Amino-acid change
ENST00000233710.4:c.993A= MANE Select ENSP00000233710.3:p.Gln331=
ENST00000652584.1:n.1221A=
ENST00000233710.3:c.993A= ENSP00000233710.3:p.Gln331=
NM_001608.3:c.993A= NP_001599.1:p.Gln331=
XM_005246517.3:c.930A= XP_005246574.1:p.Gln310=
XM_005246517.4:c.930A= XP_005246574.1:p.Gln310=
XM_017003955.1:c.570A= XP_016859444.1:p.Gln190=
NM_001608.4:c.993A= MANE Select NP_001599.1:p.Gln331=