Canonical Allele Identifier: CA10626661
Gene: RPS10 HGNC NCBI
RPS10-NUDT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34426052G>C , CM000668.2:g.34426052G>C GRCh38
NC_000006.11:g.34393829G>C , CM000668.1:g.34393829G>C GRCh37
NC_000006.10:g.34501807G>C NCBI36
NG_023200.1:g.5048C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344700.8:c.-21C>G (RPS10) ENSP00000363169.1:n.-21C>G
ENST00000639725.1:c.-21C>G (RPS10-NUDT3) ENSP00000492441.1:n.-21C>G
ENST00000644393.1:c.-21C>G (RPS10) ENSP00000496022.1:n.-21C>G
ENST00000644700.1:c.-21C>G (RPS10) ENSP00000495142.1:n.-21C>G
ENST00000648437.1:c.-21C>G (RPS10) MANE Select ENSP00000497917.1:n.-21C>G
ENST00000326199.12:c.-21C>G (RPS10) ENSP00000347271.6:n.-21C>G
NM_001014.4:c.-21C>G (RPS10) NP_001005.1:n.-21C>G
NM_001202470.2:c.-21C>G (RPS10-NUDT3) NP_001189399.1:n.-21C>G
NM_001204091.1:c.-25C>G (RPS10) NP_001191020.1:n.-25C>G
NM_001014.5:c.-21C>G (RPS10) MANE Select NP_001005.1:n.-21C>G
NM_001203245.3:c.-257C>G (RPS10) NP_001190174.1:n.-257C>G
NM_001204091.2:c.-25C>G (RPS10) NP_001191020.1:n.-25C>G
NM_001202470.3:c.-21C>G (RPS10-NUDT3) NP_001189399.1:n.-21C>G