Canonical Allele Identifier: CA2038229675
Gene: RPS26 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56042157T= , CM000674.2:g.56042157T= GRCh38
NC_000012.11:g.56435941T= , CM000674.1:g.56435941T= GRCh37
NC_000012.10:g.54722208T= NCBI36
NG_023201.1:g.5256T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-10T= ENSP00000348849.5:n.-10T=
ENST00000646449.2:c.-10T= MANE Select ENSP00000496643.1:n.-10T=
ENST00000356464.9:c.-10T= ENSP00000348849.5:n.-10T=
ENST00000548590.1:n.18T=
ENST00000552361.1:c.-10T= ENSP00000450339.1:n.-10T=
NM_001029.3:c.-10T= NP_001020.2:n.-10T=
NM_001029.5:c.-10T= MANE Select NP_001020.2:n.-10T=
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