Canonical Allele Identifier: CA947972510
Gene: RPS26 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041721_56041722insGGGGGGGG , CM000674.2:g.56041721_56041722insGGGGGGGG GRCh38
NC_000012.11:g.56435505_56435506insGGGGGGGG , CM000674.1:g.56435505_56435506insGGGGGGGG GRCh37
NC_000012.10:g.54721772_54721773insGGGGGGGG NCBI36
NG_023201.1:g.4820_4821insGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-90_-356-89insGGGGGGGG ENSP00000348849.5:n.-356-90_-356-89insGGGGGGGG
XR_944989.3:n.289_290insCCCCCCCC
XR_944990.3:n.289_290insCCCCCCCC