Canonical Allele Identifier: CA3765153

Gene: RPS10 RPS10-NUDT3

Linked Data

• ClinVar Variation Id: 516588
• ClinVar RCV Id: RCV002498974
• dbSNP Id: rs115481077
• ExAC: 6:34393016 T / C
• gnomAD v2: 6-34393016-T-C
• gnomAD v3: 6-34425239-T-C
• gnomAD v4: 6-34425239-T-C
• MyVariant Identifiers: chr6:g.34393016T>C (hg19) ; chr6:g.34425239T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.34425239T>C , CM000668.2:g.34425239T>C	GRCh38
NC_000006.11:g.34393016T>C , CM000668.1:g.34393016T>C	GRCh37
NC_000006.10:g.34500994T>C	NCBI36
NG_023200.1:g.5861A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000344700.8:c.1-18A>G (RPS10)	ENSP00000363169.1:n.1-18A>G
ENST00000494077.6:c.1-18A>G (RPS10-NUDT3)	ENSP00000495405.1:n.1-18A>G
ENST00000621356.3:c.1-18A>G (RPS10)	ENSP00000481646.1:n.1-18A>G
ENST00000639725.1:c.1-18A>G (RPS10-NUDT3)	ENSP00000492441.1:n.1-18A>G
ENST00000639877.1:c.1-18A>G (RPS10-NUDT3)	ENSP00000491891.1:n.1-18A>G
ENST00000644393.1:c.1-18A>G (RPS10)	ENSP00000496022.1:n.1-18A>G
ENST00000644700.1:c.1-18A>G (RPS10)	ENSP00000495142.1:n.1-18A>G
ENST00000648437.1:c.1-18A>G (RPS10) MANE Select	ENSP00000497917.1:n.1-18A>G
ENST00000326199.12:c.1-18A>G (RPS10)	ENSP00000347271.6:n.1-18A>G
ENST00000464218.5:n.66-18A>G (RPS10)
ENST00000467531.5:n.228-18A>G (RPS10)
ENST00000480942.1:n.20-18A>G (RPS10)
ENST00000494077.5:n.232-18A>G (RPS10)
ENST00000605528.1:c.1-18A>G (RPS10-NUDT3)	ENSP00000475027.1:n.1-18A>G
ENST00000621356.2:c.1-18A>G (RPS10)	ENSP00000481646.1:n.1-18A>G
NM_001014.4:c.1-18A>G (RPS10)	NP_001005.1:n.1-18A>G
NM_001202470.2:c.1-18A>G (RPS10-NUDT3)	NP_001189399.1:n.1-18A>G
NM_001203245.2:c.1-18A>G (RPS10)	NP_001190174.1:n.1-18A>G
NM_001204091.1:c.1-18A>G (RPS10)	NP_001191020.1:n.1-18A>G
NM_001014.5:c.1-18A>G (RPS10) MANE Select	NP_001005.1:n.1-18A>G
NM_001203245.3:c.1-18A>G (RPS10)	NP_001190174.1:n.1-18A>G
NM_001204091.2:c.1-18A>G (RPS10)	NP_001191020.1:n.1-18A>G
NM_001202470.3:c.1-18A>G (RPS10-NUDT3)	NP_001189399.1:n.1-18A>G