Canonical Allele Identifier: CA2067555958
Gene: ACADS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739559G= , CM000674.2:g.120739559G= GRCh38
NC_000012.11:g.121177362G= , CM000674.1:g.121177362G= GRCh37
NC_000012.10:g.119661745G= NCBI36
NG_007991.1:g.18792G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.*111G= MANE Select ENSP00000242592.4:n.*111G=
ENST00000242592.8:c.*111G= ENSP00000242592.4:n.*111G=
ENST00000411593.2:c.*111G= ENSP00000401045.2:n.*111G=
NM_000017.3:c.*111G= NP_000008.1:n.*111G=
NM_001302554.1:c.*111G= NP_001289483.1:n.*111G=
NM_000017.4:c.*111G= MANE Select NP_000008.1:n.*111G=
NM_001302554.2:c.*111G= NP_001289483.1:n.*111G=
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