Canonical Allele Identifier: CA253791
Gene: RPS10 HGNC NCBI
RPS10-NUDT3 HGNC NCBI

Linked Data

ClinVar Variation Id: 6187
dbSNP Id: rs267607022

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34421793G>A , CM000668.2:g.34421793G>A GRCh38
NC_000006.11:g.34389570G>A , CM000668.1:g.34389570G>A GRCh37
NC_000006.10:g.34497548G>A NCBI36
NG_023200.1:g.9307C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000344700.8:c.337C>T (RPS10) ENSP00000363169.1:p.Arg113Ter
ENST00000494077.6:c.337C>T (RPS10-NUDT3) ENSP00000495405.1:p.Arg113Ter
ENST00000605528.2:c.264C>T (RPS10-NUDT3)
ENST00000621356.3:c.337C>T (RPS10) ENSP00000481646.1:p.Arg113Ter
ENST00000639725.1:c.337C>T (RPS10-NUDT3) ENSP00000492441.1:p.Arg113Ter
ENST00000639877.1:c.337C>T (RPS10-NUDT3) ENSP00000491891.1:p.Arg113Ter
ENST00000644393.1:c.337C>T (RPS10) ENSP00000496022.1:p.Arg113Ter
ENST00000644700.1:c.337C>T (RPS10) ENSP00000495142.1:p.Arg113Ter
ENST00000648437.1:c.337C>T (RPS10) MANE Select ENSP00000497917.1:p.Arg113Ter
ENST00000326199.12:c.337C>T (RPS10) ENSP00000347271.6:p.Arg113Ter
ENST00000344700.7:c.337C>T (RPS10) ENSP00000363169.1:p.Arg113Ter
ENST00000464218.5:n.402C>T (RPS10)
ENST00000467531.5:n.564C>T (RPS10)
ENST00000494077.5:n.568C>T (RPS10)
ENST00000605528.1:c.337C>T (RPS10-NUDT3) ENSP00000475027.1:p.Arg113Ter
ENST00000621356.2:c.337C>T (RPS10) ENSP00000481646.1:p.Arg113Ter
NM_001014.4:c.337C>T (RPS10) NP_001005.1:p.Arg113Ter
NM_001202470.2:c.337C>T (RPS10-NUDT3) NP_001189399.1:p.Arg113Ter
NM_001203245.2:c.337C>T (RPS10) NP_001190174.1:p.Arg113Ter
NM_001204091.1:c.337C>T (RPS10) NP_001191020.1:p.Arg113Ter
NM_001014.5:c.337C>T (RPS10) MANE Select NP_001005.1:p.Arg113Ter
NM_001203245.3:c.337C>T (RPS10) NP_001190174.1:p.Arg113Ter
NM_001204091.2:c.337C>T (RPS10) NP_001191020.1:p.Arg113Ter
NM_001202470.3:c.337C>T (RPS10-NUDT3) NP_001189399.1:p.Arg113Ter