Canonical Allele Identifier: CA2067555451
Gene: ACADS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738711C= , CM000674.2:g.120738711C= GRCh38
NC_000012.11:g.121176514C= , CM000674.1:g.121176514C= GRCh37
NC_000012.10:g.119660897C= NCBI36
NG_007991.1:g.17944C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.933+41C= MANE Select ENSP00000242592.4:n.933+41C=
ENST00000242592.8:c.933+41C= ENSP00000242592.4:n.933+41C=
ENST00000411593.2:c.921+41C= ENSP00000401045.2:n.921+41C=
NM_000017.3:c.933+41C= NP_000008.1:n.933+41C=
NM_001302554.1:c.921+41C= NP_001289483.1:n.921+41C=
NM_000017.4:c.933+41C= MANE Select NP_000008.1:n.933+41C=
NM_001302554.2:c.921+41C= NP_001289483.1:n.921+41C=
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