Canonical Allele Identifier: CA2038228851
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041513_56041515delinsAAT , CM000674.2:g.56041513_56041515delinsAAT GRCh38
NC_000012.11:g.56435297_56435299delinsAAT , CM000674.1:g.56435297_56435299delinsAAT GRCh37
NC_000012.10:g.54721564_54721566delinsAAT NCBI36
NG_023201.1:g.4612_4614delinsAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+117_-357+119delinsAAT ENSP00000348849.5:n.-357+117_-357+119delinsAAT
XR_944989.1:n.198_200delinsATT
XR_944990.1:n.198_200delinsATT
XR_944989.3:n.489_491delinsATT
XR_944990.3:n.489_491delinsATT