Canonical Allele Identifier: CA2089833519
Gene: NUDT15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045591G= , CM000675.2:g.48045591G= GRCh38
NC_000013.10:g.48619727G= , CM000675.1:g.48619727G= GRCh37
NC_000013.9:g.47517728G= NCBI36
NG_047021.1:g.13025G=

Transcript Alleles

HGVS Amino-acid change
ENST00000258662.3:c.356-69G= MANE Select ENSP00000258662.1:n.356-69G=
ENST00000258662.2:c.356-69G= ENSP00000258662.1:n.356-69G=
NM_018283.2:c.356-69G= NP_060753.1:n.356-69G=
NM_018283.3:c.356-69G= NP_060753.1:n.356-69G=
NR_136687.1:n.536-69G=
NR_136688.1:n.536-69G=
NM_018283.4:c.356-69G= MANE Select NP_060753.1:n.356-69G=
NR_136687.2:n.377-69G=
NR_136688.2:n.377-69G=