Canonical Allele Identifier: CA2067556025
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739715G= , CM000674.2:g.120739715G= GRCh38
NC_000012.11:g.121177518G= , CM000674.1:g.121177518G= GRCh37
NC_000012.10:g.119661901G= NCBI36
NG_007991.1:g.18948G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.*267G= MANE Select ENSP00000242592.4:n.*267G=
ENST00000242592.8:c.*267G= ENSP00000242592.4:n.*267G=
NM_000017.3:c.*267G= NP_000008.1:n.*267G=
NM_001302554.1:c.*267G= NP_001289483.1:n.*267G=
NM_000017.4:c.*267G= MANE Select NP_000008.1:n.*267G=
NM_001302554.2:c.*267G= NP_001289483.1:n.*267G=