Canonical Allele Identifier: CA2621371190
Gene: ACADS HGNC NCBI

Linked Data

gnomAD v4: 12-120739639-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739639T>C , CM000674.2:g.120739639T>C GRCh38
NC_000012.11:g.121177442T>C , CM000674.1:g.121177442T>C GRCh37
NC_000012.10:g.119661825T>C NCBI36
NG_007991.1:g.18872T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.*191T>C MANE Select ENSP00000242592.4:n.*191T>C
ENST00000242592.8:c.*191T>C ENSP00000242592.4:n.*191T>C
NM_000017.3:c.*191T>C NP_000008.1:n.*191T>C
NM_001302554.1:c.*191T>C NP_001289483.1:n.*191T>C
NM_000017.4:c.*191T>C MANE Select NP_000008.1:n.*191T>C
NM_001302554.2:c.*191T>C NP_001289483.1:n.*191T>C
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