Canonical Allele Identifier: CA2067556031
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739720G= , CM000674.2:g.120739720G= GRCh38
NC_000012.11:g.121177523G= , CM000674.1:g.121177523G= GRCh37
NC_000012.10:g.119661906G= NCBI36
NG_007991.1:g.18953G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.*272G= MANE Select ENSP00000242592.4:n.*272G=
ENST00000242592.8:c.*272G= ENSP00000242592.4:n.*272G=
NM_000017.3:c.*272G= NP_000008.1:n.*272G=
NM_001302554.1:c.*272G= NP_001289483.1:n.*272G=
NM_000017.4:c.*272G= MANE Select NP_000008.1:n.*272G=
NM_001302554.2:c.*272G= NP_001289483.1:n.*272G=