Canonical Allele Identifier: CA2621370264
Gene: ACADS HGNC NCBI

Linked Data

gnomAD v4: 12-120739248-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739248T>G , CM000674.2:g.120739248T>G GRCh38
NC_000012.11:g.121177051T>G , CM000674.1:g.121177051T>G GRCh37
NC_000012.10:g.119661434T>G NCBI36
NG_007991.1:g.18481T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.1087-48T>G MANE Select ENSP00000242592.4:n.1087-48T>G
ENST00000242592.8:c.1087-48T>G ENSP00000242592.4:n.1087-48T>G
ENST00000411593.2:c.1075-48T>G ENSP00000401045.2:n.1075-48T>G
NM_000017.3:c.1087-48T>G NP_000008.1:n.1087-48T>G
NM_001302554.1:c.1075-48T>G NP_001289483.1:n.1075-48T>G
NM_000017.4:c.1087-48T>G MANE Select NP_000008.1:n.1087-48T>G
NM_001302554.2:c.1075-48T>G NP_001289483.1:n.1075-48T>G
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