Canonical Allele Identifier: CA1620414894
Gene: RPS10-NUDT3 HGNC NCBI
NUDT3 HGNC NCBI

Linked Data

dbSNP Id: rs1764188333
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34335055_34335058del , CM000668.2:g.34335055_34335058del GRCh38
NC_000006.11:g.34302832_34302835del , CM000668.1:g.34302832_34302835del GRCh37
NC_000006.10:g.34410810_34410813del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000605528.2:c.384-39371_384-39368del (RPS10-NUDT3)
ENST00000607016.2:c.210+6806_210+6809del (NUDT3) MANE Select ENSP00000476119.1:n.210+6806_210+6809del
ENST00000639725.1:c.567+6806_567+6809del (RPS10-NUDT3) ENSP00000492441.1:n.567+6806_567+6809del
ENST00000639877.1:c.567+6806_567+6809del (RPS10-NUDT3) ENSP00000491891.1:n.567+6806_567+6809del
ENST00000605528.1:c.567+6806_567+6809del (RPS10-NUDT3) ENSP00000475027.1:n.567+6806_567+6809del
ENST00000607016.1:c.210+6806_210+6809del (NUDT3) ENSP00000476119.1:n.210+6806_210+6809del
NM_001202470.2:c.567+6806_567+6809del (RPS10-NUDT3) NP_001189399.1:n.567+6806_567+6809del
NM_006703.3:c.210+6806_210+6809del (NUDT3) NP_006694.1:n.210+6806_210+6809del
NM_006703.4:c.210+6806_210+6809del (NUDT3) MANE Select NP_006694.1:n.210+6806_210+6809del
NM_001202470.3:c.567+6806_567+6809del (RPS10-NUDT3) NP_001189399.1:n.567+6806_567+6809del
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