Canonical Allele Identifier: CA566454825
Gene: RPS10-NUDT3 HGNC NCBI
NUDT3 HGNC NCBI

Linked Data

dbSNP Id: rs1414591175
gnomAD v2: 6-34302884-T-G
gnomAD v3: 6-34335107-T-G
gnomAD v4: 6-34335107-T-G
MyVariant Identifiers: chr6:g.34302884T>G (hg19) chr6:g.34335107T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34335107T>G , CM000668.2:g.34335107T>G GRCh38
NC_000006.11:g.34302884T>G , CM000668.1:g.34302884T>G GRCh37
NC_000006.10:g.34410862T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000605528.2:c.384-39422A>C (RPS10-NUDT3)
ENST00000607016.2:c.210+6755A>C (NUDT3) MANE Select ENSP00000476119.1:n.210+6755A>C
ENST00000639725.1:c.567+6755A>C (RPS10-NUDT3) ENSP00000492441.1:n.567+6755A>C
ENST00000639877.1:c.567+6755A>C (RPS10-NUDT3) ENSP00000491891.1:n.567+6755A>C
ENST00000605528.1:c.567+6755A>C (RPS10-NUDT3) ENSP00000475027.1:n.567+6755A>C
ENST00000607016.1:c.210+6755A>C (NUDT3) ENSP00000476119.1:n.210+6755A>C
NM_001202470.2:c.567+6755A>C (RPS10-NUDT3) NP_001189399.1:n.567+6755A>C
NM_006703.3:c.210+6755A>C (NUDT3) NP_006694.1:n.210+6755A>C
NM_006703.4:c.210+6755A>C (NUDT3) MANE Select NP_006694.1:n.210+6755A>C
NM_001202470.3:c.567+6755A>C (RPS10-NUDT3) NP_001189399.1:n.567+6755A>C
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