Canonical Allele Identifier: CA2089833514
Gene: NUDT15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045566A= , CM000675.2:g.48045566A= GRCh38
NC_000013.10:g.48619702A= , CM000675.1:g.48619702A= GRCh37
NC_000013.9:g.47517703A= NCBI36
NG_047021.1:g.13000A=

Transcript Alleles

HGVS Amino-acid change
ENST00000258662.3:c.356-94A= MANE Select ENSP00000258662.1:n.356-94A=
ENST00000258662.2:c.356-94A= ENSP00000258662.1:n.356-94A=
NM_018283.2:c.356-94A= NP_060753.1:n.356-94A=
NM_018283.3:c.356-94A= NP_060753.1:n.356-94A=
NR_136687.1:n.536-94A=
NR_136688.1:n.536-94A=
NM_018283.4:c.356-94A= MANE Select NP_060753.1:n.356-94A=
NR_136687.2:n.377-94A=
NR_136688.2:n.377-94A=