Canonical Allele Identifier: CA2621368812
Gene: ACADS HGNC NCBI

Linked Data

gnomAD v4: 12-120738683-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738683G>A , CM000674.2:g.120738683G>A GRCh38
NC_000012.11:g.121176486G>A , CM000674.1:g.121176486G>A GRCh37
NC_000012.10:g.119660869G>A NCBI36
NG_007991.1:g.17916G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.933+13G>A MANE Select ENSP00000242592.4:n.933+13G>A
ENST00000242592.8:c.933+13G>A ENSP00000242592.4:n.933+13G>A
ENST00000411593.2:c.921+13G>A ENSP00000401045.2:n.921+13G>A
NM_000017.3:c.933+13G>A NP_000008.1:n.933+13G>A
NM_001302554.1:c.921+13G>A NP_001289483.1:n.921+13G>A
NM_000017.4:c.933+13G>A MANE Select NP_000008.1:n.933+13G>A
NM_001302554.2:c.921+13G>A NP_001289483.1:n.921+13G>A
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