Canonical Allele Identifier: CA388154071
Gene: NUDT15 HGNC NCBI

Linked Data

COSMIC: COSM5006643
MyVariant Identifiers: chr13:g.48619802A>G (hg19) chr13:g.48045666A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045666A>G , CM000675.2:g.48045666A>G GRCh38
NC_000013.10:g.48619802A>G , CM000675.1:g.48619802A>G GRCh37
NC_000013.9:g.47517803A>G NCBI36
NG_047021.1:g.13100A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000258662.3:c.362A>G MANE Select ENSP00000258662.1:p.Glu121Gly
ENST00000258662.2:c.362A>G ENSP00000258662.1:p.Glu121Gly
NM_018283.2:c.362A>G NP_060753.1:p.Glu121Gly
NM_018283.3:c.362A>G NP_060753.1:p.Glu121Gly
NR_136687.1:n.542A>G
NR_136688.1:n.542A>G
NM_018283.4:c.362A>G MANE Select NP_060753.1:p.Glu121Gly
NR_136687.2:n.383A>G
NR_136688.2:n.383A>G
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