Canonical Allele Identifier: CA2038228868
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041537_56041545delinsCATTGTGGG , CM000674.2:g.56041537_56041545delinsCATTGTGGG GRCh38
NC_000012.11:g.56435321_56435329delinsCATTGTGGG , CM000674.1:g.56435321_56435329delinsCATTGTGGG GRCh37
NC_000012.10:g.54721588_54721596delinsCATTGTGGG NCBI36
NG_023201.1:g.4636_4644delinsCATTGTGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+141_-357+149delinsCATTGTGGG ENSP00000348849.5:n.-357+141_-357+149delinsCATTGTGGG
XR_944989.1:n.168_176delinsCCCACAATG
XR_944990.1:n.168_176delinsCCCACAATG
XR_944989.3:n.459_467delinsCCCACAATG
XR_944990.3:n.459_467delinsCCCACAATG