Canonical Allele Identifier: CA2038229746
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56042174_56042177delinsGTCT , CM000674.2:g.56042174_56042177delinsGTCT GRCh38
NC_000012.11:g.56435958_56435961delinsGTCT , CM000674.1:g.56435958_56435961delinsGTCT GRCh37
NC_000012.10:g.54722225_54722228delinsGTCT NCBI36
NG_023201.1:g.5273_5276delinsGTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.3+5_3+8delinsGTCT ENSP00000348849.5:n.3+5_3+8delinsGTCT
ENST00000646449.2:c.3+5_3+8delinsGTCT MANE Select ENSP00000496643.1:n.3+5_3+8delinsGTCT
ENST00000356464.9:c.3+5_3+8delinsGTCT ENSP00000348849.5:n.3+5_3+8delinsGTCT
ENST00000548590.1:n.30+5_30+8delinsGTCT
ENST00000552361.1:c.3+5_3+8delinsGTCT ENSP00000450339.1:n.3+5_3+8delinsGTCT
NM_001029.3:c.3+5_3+8delinsGTCT NP_001020.2:n.3+5_3+8delinsGTCT
NM_001029.5:c.3+5_3+8delinsGTCT MANE Select NP_001020.2:n.3+5_3+8delinsGTCT