Canonical Allele Identifier: CA388154112
Gene: NUDT15 HGNC NCBI

Linked Data

dbSNP Id: rs1412814385
MyVariant Identifiers: chr13:g.48619810C>G (hg19) chr13:g.48045674C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045674C>G , CM000675.2:g.48045674C>G GRCh38
NC_000013.10:g.48619810C>G , CM000675.1:g.48619810C>G GRCh37
NC_000013.9:g.47517811C>G NCBI36
NG_047021.1:g.13108C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258662.3:c.370C>G MANE Select ENSP00000258662.1:p.Pro124Ala
ENST00000258662.2:c.370C>G ENSP00000258662.1:p.Pro124Ala
NM_018283.2:c.370C>G NP_060753.1:p.Pro124Ala
NM_018283.3:c.370C>G NP_060753.1:p.Pro124Ala
NR_136687.1:n.550C>G
NR_136688.1:n.550C>G
NM_018283.4:c.370C>G MANE Select NP_060753.1:p.Pro124Ala
NR_136687.2:n.391C>G
NR_136688.2:n.391C>G
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