Canonical Allele Identifier: CA1559205546

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.82276423T= , CM000667.2:g.82276423T= GRCh38
NC_000005.9:g.81572242T= , CM000667.1:g.81572242T= GRCh37
NC_000005.8:g.81607998T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296674.13:c.260A= (RPS23) MANE Select ENSP00000296674.8:p.Asn87=
ENST00000651545.1:c.260A= (RPS23) ENSP00000498621.1:p.Asn87=
ENST00000296674.12:c.260A= (RPS23) ENSP00000296674.8:p.Asn87=
ENST00000503605.1:n.469A= (RPS23)
ENST00000504293.5:n.355A= (RPS23)
ENST00000507980.1:c.260A= (RPS23) ENSP00000422071.1:p.Asn87=
ENST00000510019.5:c.232+28A= (RPS23) ENSP00000425833.1:n.232+28A=
ENST00000510210.5:c.260A= (RPS23) ENSP00000427043.1:p.Asn87=
ENST00000512493.5:c.260A= (RPS23) ENSP00000425865.1:p.Asn87=
ENST00000514253.2:n.470T= (ATG10)
NM_001025.4:c.260A= (RPS23) NP_001016.1:p.Asn87=
NM_001025.5:c.260A= (RPS23) MANE Select NP_001016.1:p.Asn87=