Canonical Allele Identifier: CA2089833629
Gene: NUDT15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045825T= , CM000675.2:g.48045825T= GRCh38
NC_000013.10:g.48619961T= , CM000675.1:g.48619961T= GRCh37
NC_000013.9:g.47517962T= NCBI36
NG_047021.1:g.13259T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258662.3:c.*26T= MANE Select ENSP00000258662.1:n.*26T=
ENST00000258662.2:c.*26T= ENSP00000258662.1:n.*26T=
NM_018283.2:c.*26T= NP_060753.1:n.*26T=
NM_018283.3:c.*26T= NP_060753.1:n.*26T=
NR_136687.1:n.701T=
NR_136688.1:n.675+26T=
NM_018283.4:c.*26T= MANE Select NP_060753.1:n.*26T=
NR_136687.2:n.542T=
NR_136688.2:n.516+26T=
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