Canonical Allele Identifier: CA2619258788
Gene: RPS26 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041913del , CM000674.2:g.56041913del GRCh38
NC_000012.11:g.56435697del , CM000674.1:g.56435697del GRCh37
NC_000012.10:g.54721964del NCBI36
NG_023201.1:g.5012del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-254del ENSP00000348849.5:n.-254del
ENST00000356464.9:c.-254del ENSP00000348849.5:n.-254del
ENST00000552361.1:c.-186del ENSP00000450339.1:n.-186del
NM_001029.3:c.-254del NP_001020.2:n.-254del
XR_944989.3:n.92del
XR_944990.3:n.92del