Canonical Allele Identifier: CA2089833698
Gene: NUDT15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045998T= , CM000675.2:g.48045998T= GRCh38
NC_000013.10:g.48620134T= , CM000675.1:g.48620134T= GRCh37
NC_000013.9:g.47518135T= NCBI36
NG_047021.1:g.13432T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258662.3:c.*199T= MANE Select ENSP00000258662.1:n.*199T=
ENST00000258662.2:c.*199T= ENSP00000258662.1:n.*199T=
NM_018283.2:c.*199T= NP_060753.1:n.*199T=
NM_018283.3:c.*199T= NP_060753.1:n.*199T=
NR_136687.1:n.718+156T=
NR_136688.1:n.675+199T=
NM_018283.4:c.*199T= MANE Select NP_060753.1:n.*199T=
NR_136687.2:n.559+156T=
NR_136688.2:n.516+199T=
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