Canonical Allele Identifier: CA2621369794
Gene: ACADS HGNC NCBI

Linked Data

gnomAD v4: 12-120739019-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739022del , CM000674.2:g.120739022del GRCh38
NC_000012.11:g.121176825del , CM000674.1:g.121176825del GRCh37
NC_000012.10:g.119661208del NCBI36
NG_007991.1:g.18255del

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.1029+107del MANE Select ENSP00000242592.4:n.1029+107del
ENST00000242592.8:c.1029+107del ENSP00000242592.4:n.1029+107del
ENST00000411593.2:c.1017+107del ENSP00000401045.2:n.1017+107del
NM_000017.3:c.1029+107del NP_000008.1:n.1029+107del
NM_001302554.1:c.1017+107del NP_001289483.1:n.1017+107del
NM_000017.4:c.1029+107del MANE Select NP_000008.1:n.1029+107del
NM_001302554.2:c.1017+107del NP_001289483.1:n.1017+107del
Search 100 bp 5'
Search 100 bp 3'