Canonical Allele Identifier: CA2067556022
Gene: ACADS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739711G= , CM000674.2:g.120739711G= GRCh38
NC_000012.11:g.121177514G= , CM000674.1:g.121177514G= GRCh37
NC_000012.10:g.119661897G= NCBI36
NG_007991.1:g.18944G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.*263G= MANE Select ENSP00000242592.4:n.*263G=
ENST00000242592.8:c.*263G= ENSP00000242592.4:n.*263G=
NM_000017.3:c.*263G= NP_000008.1:n.*263G=
NM_001302554.1:c.*263G= NP_001289483.1:n.*263G=
NM_000017.4:c.*263G= MANE Select NP_000008.1:n.*263G=
NM_001302554.2:c.*263G= NP_001289483.1:n.*263G=
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