Canonical Allele Identifier: CA2621371137
Gene: ACADS HGNC NCBI

Linked Data

gnomAD v4: 12-120739608-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739608T>G , CM000674.2:g.120739608T>G GRCh38
NC_000012.11:g.121177411T>G , CM000674.1:g.121177411T>G GRCh37
NC_000012.10:g.119661794T>G NCBI36
NG_007991.1:g.18841T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.*160T>G MANE Select ENSP00000242592.4:n.*160T>G
ENST00000242592.8:c.*160T>G ENSP00000242592.4:n.*160T>G
NM_000017.3:c.*160T>G NP_000008.1:n.*160T>G
NM_001302554.1:c.*160T>G NP_001289483.1:n.*160T>G
NM_000017.4:c.*160T>G MANE Select NP_000008.1:n.*160T>G
NM_001302554.2:c.*160T>G NP_001289483.1:n.*160T>G
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