Canonical Allele Identifier: CA2067555426
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738649C= , CM000674.2:g.120738649C= GRCh38
NC_000012.11:g.121176452C= , CM000674.1:g.121176452C= GRCh37
NC_000012.10:g.119660835C= NCBI36
NG_007991.1:g.17882C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.912C= MANE Select ENSP00000242592.4:p.Leu304=
ENST00000242592.8:c.912C= ENSP00000242592.4:p.Leu304=
ENST00000411593.2:c.900C= ENSP00000401045.2:p.Leu300=
NM_000017.3:c.912C= NP_000008.1:p.Leu304=
NM_001302554.1:c.900C= NP_001289483.1:p.Leu300=
NM_000017.4:c.912C= MANE Select NP_000008.1:p.Leu304=
NM_001302554.2:c.900C= NP_001289483.1:p.Leu300=