Canonical Allele Identifier: CA2067556018
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739708_120739709delinsTG , CM000674.2:g.120739708_120739709delinsTG GRCh38
NC_000012.11:g.121177511_121177512delinsTG , CM000674.1:g.121177511_121177512delinsTG GRCh37
NC_000012.10:g.119661894_119661895delinsTG NCBI36
NG_007991.1:g.18941_18942delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.*260_*261delinsTG MANE Select ENSP00000242592.4:n.*260_*261delinsTG
ENST00000242592.8:c.*260_*261delinsTG ENSP00000242592.4:n.*260_*261delinsTG
NM_000017.3:c.*260_*261delinsTG NP_000008.1:n.*260_*261delinsTG
NM_001302554.1:c.*260_*261delinsTG NP_001289483.1:n.*260_*261delinsTG
NM_000017.4:c.*260_*261delinsTG MANE Select NP_000008.1:n.*260_*261delinsTG
NM_001302554.2:c.*260_*261delinsTG NP_001289483.1:n.*260_*261delinsTG