Canonical Allele Identifier: CA2038229511
Gene: RPS26 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56042068C= , CM000674.2:g.56042068C= GRCh38
NC_000012.11:g.56435852C= , CM000674.1:g.56435852C= GRCh37
NC_000012.10:g.54722119C= NCBI36
NG_023201.1:g.5167C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-99C= ENSP00000348849.5:n.-99C=
ENST00000646449.2:c.-99C= MANE Select ENSP00000496643.1:n.-99C=
ENST00000356464.9:c.-99C= ENSP00000348849.5:n.-99C=
ENST00000552361.1:c.-35+4C= ENSP00000450339.1:n.-35+4C=
NM_001029.3:c.-99C= NP_001020.2:n.-99C=
NM_001029.5:c.-99C= MANE Select NP_001020.2:n.-99C=
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