Canonical Allele Identifier: CA2067556000
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739686T= , CM000674.2:g.120739686T= GRCh38
NC_000012.11:g.121177489T= , CM000674.1:g.121177489T= GRCh37
NC_000012.10:g.119661872T= NCBI36
NG_007991.1:g.18919T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.*238T= MANE Select ENSP00000242592.4:n.*238T=
ENST00000242592.8:c.*238T= ENSP00000242592.4:n.*238T=
NM_000017.3:c.*238T= NP_000008.1:n.*238T=
NM_001302554.1:c.*238T= NP_001289483.1:n.*238T=
NM_000017.4:c.*238T= MANE Select NP_000008.1:n.*238T=
NM_001302554.2:c.*238T= NP_001289483.1:n.*238T=