Canonical Allele Identifier: CA2621371458
Gene: ACADS HGNC NCBI

Linked Data

gnomAD v4: 12-120739708-T-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739708T>A , CM000674.2:g.120739708T>A GRCh38
NC_000012.11:g.121177511T>A , CM000674.1:g.121177511T>A GRCh37
NC_000012.10:g.119661894T>A NCBI36
NG_007991.1:g.18941T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.*260T>A MANE Select ENSP00000242592.4:n.*260T>A
ENST00000242592.8:c.*260T>A ENSP00000242592.4:n.*260T>A
NM_000017.3:c.*260T>A NP_000008.1:n.*260T>A
NM_001302554.1:c.*260T>A NP_001289483.1:n.*260T>A
NM_000017.4:c.*260T>A MANE Select NP_000008.1:n.*260T>A
NM_001302554.2:c.*260T>A NP_001289483.1:n.*260T>A
Search 100 bp 5'
Search 100 bp 3'