Canonical Allele Identifier: CA1559205593

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.82276478A= , CM000667.2:g.82276478A= GRCh38
NC_000005.9:g.81572297A= , CM000667.1:g.81572297A= GRCh37
NC_000005.8:g.81608053A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296674.13:c.205T= (RPS23) MANE Select ENSP00000296674.8:p.Cys69=
ENST00000651545.1:c.205T= (RPS23) ENSP00000498621.1:p.Cys69=
ENST00000296674.12:c.205T= (RPS23) ENSP00000296674.8:p.Cys69=
ENST00000503605.1:n.414T= (RPS23)
ENST00000504293.5:n.300T= (RPS23)
ENST00000507980.1:c.205T= (RPS23) ENSP00000422071.1:p.Cys69=
ENST00000510019.5:c.205T= (RPS23) ENSP00000425833.1:p.Cys69=
ENST00000510210.5:c.205T= (RPS23) ENSP00000427043.1:p.Cys69=
ENST00000512493.5:c.205T= (RPS23) ENSP00000425865.1:p.Cys69=
ENST00000514253.2:n.525A= (ATG10)
NM_001025.4:c.205T= (RPS23) NP_001016.1:p.Cys69=
NM_001025.5:c.205T= (RPS23) MANE Select NP_001016.1:p.Cys69=