Canonical Allele Identifier: CA2067553087
Gene: ACADS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120736943C= , CM000674.2:g.120736943C= GRCh38
NC_000012.11:g.121174746C= , CM000674.1:g.121174746C= GRCh37
NC_000012.10:g.119659129C= NCBI36
NG_007991.1:g.16176C=

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.211-43C= MANE Select ENSP00000242592.4:n.211-43C=
ENST00000242592.8:c.211-43C= ENSP00000242592.4:n.211-43C=
ENST00000411593.2:c.211-43C= ENSP00000401045.2:n.211-43C=
ENST00000539690.1:n.323-43C=
NM_000017.3:c.211-43C= NP_000008.1:n.211-43C=
NM_001302554.1:c.211-43C= NP_001289483.1:n.211-43C=
NM_000017.4:c.211-43C= MANE Select NP_000008.1:n.211-43C=
NM_001302554.2:c.211-43C= NP_001289483.1:n.211-43C=
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