Canonical Allele Identifier: CA2038228942
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041612_56041614delinsATC , CM000674.2:g.56041612_56041614delinsATC GRCh38
NC_000012.11:g.56435396_56435398delinsATC , CM000674.1:g.56435396_56435398delinsATC GRCh37
NC_000012.10:g.54721663_54721665delinsATC NCBI36
NG_023201.1:g.4711_4713delinsATC

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-199_-356-197delinsATC ENSP00000348849.5:n.-356-199_-356-197delinsATC
XR_944989.1:n.99_101delinsGAT
XR_944990.1:n.99_101delinsGAT
XR_944989.3:n.390_392delinsGAT
XR_944990.3:n.390_392delinsGAT