Canonical Allele Identifier: CA2038229280
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041867_56041868delinsAT , CM000674.2:g.56041867_56041868delinsAT GRCh38
NC_000012.11:g.56435651_56435652delinsAT , CM000674.1:g.56435651_56435652delinsAT GRCh37
NC_000012.10:g.54721918_54721919delinsAT NCBI36
NG_023201.1:g.4966_4967delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-300_-299delinsAT ENSP00000348849.5:n.-300_-299delinsAT
ENST00000356464.9:c.-300_-299delinsAT ENSP00000348849.5:n.-300_-299delinsAT
XR_944989.3:n.136_137delinsAT
XR_944990.3:n.136_137delinsAT