Canonical Allele Identifier: CA2621365413
Gene: ACADS HGNC NCBI

Linked Data

gnomAD v4: 12-120736891-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120736891A>C , CM000674.2:g.120736891A>C GRCh38
NC_000012.11:g.121174694A>C , CM000674.1:g.121174694A>C GRCh37
NC_000012.10:g.119659077A>C NCBI36
NG_007991.1:g.16124A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.211-95A>C MANE Select ENSP00000242592.4:n.211-95A>C
ENST00000242592.8:c.211-95A>C ENSP00000242592.4:n.211-95A>C
ENST00000411593.2:c.211-95A>C ENSP00000401045.2:n.211-95A>C
ENST00000539690.1:n.323-95A>C
NM_000017.3:c.211-95A>C NP_000008.1:n.211-95A>C
NM_001302554.1:c.211-95A>C NP_001289483.1:n.211-95A>C
NM_000017.4:c.211-95A>C MANE Select NP_000008.1:n.211-95A>C
NM_001302554.2:c.211-95A>C NP_001289483.1:n.211-95A>C
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