Canonical Allele Identifier: CA3765138

Gene: RPS10 RPS10-NUDT3

Linked Data

• ClinVar Variation Id: 356422
• ClinVar RCV Id: RCV000309035 ; RCV001493828 ; RCV002523566
• dbSNP Id: rs201147592
• ExAC: 6:34392928 T / C
• gnomAD v2: 6-34392928-T-C
• gnomAD v3: 6-34425151-T-C
• gnomAD v4: 6-34425151-T-C
• MyVariant Identifiers: chr6:g.34392928T>C (hg19) ; chr6:g.34425151T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.34425151T>C , CM000668.2:g.34425151T>C	GRCh38
NC_000006.11:g.34392928T>C , CM000668.1:g.34392928T>C	GRCh37
NC_000006.10:g.34500906T>C	NCBI36
NG_023200.1:g.5949A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344700.8:c.71A>G (RPS10)	ENSP00000363169.1:p.Lys24Arg
ENST00000494077.6:c.71A>G (RPS10-NUDT3)	ENSP00000495405.1:p.Lys24Arg
ENST00000621356.3:c.71A>G (RPS10)	ENSP00000481646.1:p.Lys24Arg
ENST00000639725.1:c.71A>G (RPS10-NUDT3)	ENSP00000492441.1:p.Lys24Arg
ENST00000639877.1:c.71A>G (RPS10-NUDT3)	ENSP00000491891.1:p.Lys24Arg
ENST00000644393.1:c.71A>G (RPS10)	ENSP00000496022.1:p.Lys24Arg
ENST00000644700.1:c.71A>G (RPS10)	ENSP00000495142.1:p.Lys24Arg
ENST00000648437.1:c.71A>G (RPS10) MANE Select	ENSP00000497917.1:p.Lys24Arg
ENST00000326199.12:c.71A>G (RPS10)	ENSP00000347271.6:p.Lys24Arg
ENST00000344700.7:c.71A>G (RPS10)	ENSP00000363169.1:p.Lys24Arg
ENST00000464218.5:n.136A>G (RPS10)
ENST00000467531.5:n.298A>G (RPS10)
ENST00000480942.1:n.90A>G (RPS10)
ENST00000494077.5:n.302A>G (RPS10)
ENST00000605528.1:c.71A>G (RPS10-NUDT3)	ENSP00000475027.1:p.Lys24Arg
ENST00000621356.2:c.71A>G (RPS10)	ENSP00000481646.1:p.Lys24Arg
NM_001014.4:c.71A>G (RPS10)	NP_001005.1:p.Lys24Arg
NM_001202470.2:c.71A>G (RPS10-NUDT3)	NP_001189399.1:p.Lys24Arg
NM_001203245.2:c.71A>G (RPS10)	NP_001190174.1:p.Lys24Arg
NM_001204091.1:c.71A>G (RPS10)	NP_001191020.1:p.Lys24Arg
NM_001014.5:c.71A>G (RPS10) MANE Select	NP_001005.1:p.Lys24Arg
NM_001203245.3:c.71A>G (RPS10)	NP_001190174.1:p.Lys24Arg
NM_001204091.2:c.71A>G (RPS10)	NP_001191020.1:p.Lys24Arg
NM_001202470.3:c.71A>G (RPS10-NUDT3)	NP_001189399.1:p.Lys24Arg