Canonical Allele Identifier: CA12419422
Gene: RPS10 HGNC NCBI
RPS10-NUDT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34421436G>A , CM000668.2:g.34421436G>A GRCh38
NC_000006.11:g.34389213G>A , CM000668.1:g.34389213G>A GRCh37
NC_000006.10:g.34497191G>A NCBI36
NG_023200.1:g.9664C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344700.8:c.400+294C>T (RPS10) ENSP00000363169.1:n.400+294C>T
ENST00000605528.2:c.327+294C>T (RPS10-NUDT3)
ENST00000621356.3:c.400+294C>T (RPS10) ENSP00000481646.1:n.400+294C>T
ENST00000639725.1:c.400+294C>T (RPS10-NUDT3) ENSP00000492441.1:n.400+294C>T
ENST00000639877.1:c.400+294C>T (RPS10-NUDT3) ENSP00000491891.1:n.400+294C>T
ENST00000644393.1:c.400+294C>T (RPS10) ENSP00000496022.1:n.400+294C>T
ENST00000644700.1:c.400+294C>T (RPS10) ENSP00000495142.1:n.400+294C>T
ENST00000648437.1:c.400+294C>T (RPS10) MANE Select ENSP00000497917.1:n.400+294C>T
ENST00000326199.12:c.400+294C>T (RPS10) ENSP00000347271.6:n.400+294C>T
ENST00000344700.7:c.400+294C>T (RPS10) ENSP00000363169.1:n.400+294C>T
ENST00000464218.5:n.465+294C>T (RPS10)
ENST00000467531.5:n.627+294C>T (RPS10)
ENST00000494077.5:n.631+294C>T (RPS10)
ENST00000605528.1:c.400+294C>T (RPS10-NUDT3) ENSP00000475027.1:n.400+294C>T
ENST00000621356.2:c.400+294C>T (RPS10) ENSP00000481646.1:n.400+294C>T
NM_001014.4:c.400+294C>T (RPS10) NP_001005.1:n.400+294C>T
NM_001202470.2:c.400+294C>T (RPS10-NUDT3) NP_001189399.1:n.400+294C>T
NM_001203245.2:c.400+294C>T (RPS10) NP_001190174.1:n.400+294C>T
NM_001204091.1:c.400+294C>T (RPS10) NP_001191020.1:n.400+294C>T
NM_001014.5:c.400+294C>T (RPS10) MANE Select NP_001005.1:n.400+294C>T
NM_001203245.3:c.400+294C>T (RPS10) NP_001190174.1:n.400+294C>T
NM_001204091.2:c.400+294C>T (RPS10) NP_001191020.1:n.400+294C>T
NM_001202470.3:c.400+294C>T (RPS10-NUDT3) NP_001189399.1:n.400+294C>T