Canonical Allele Identifier: CA2038229117
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041728_56041729delinsGA , CM000674.2:g.56041728_56041729delinsGA GRCh38
NC_000012.11:g.56435512_56435513delinsGA , CM000674.1:g.56435512_56435513delinsGA GRCh37
NC_000012.10:g.54721779_54721780delinsGA NCBI36
NG_023201.1:g.4827_4828delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-83_-356-82delinsGA ENSP00000348849.5:n.-356-83_-356-82delinsGA
XR_944989.3:n.275_276delinsTC
XR_944990.3:n.275_276delinsTC