Canonical Allele Identifier: CA2089833590
Gene: NUDT15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045742T= , CM000675.2:g.48045742T= GRCh38
NC_000013.10:g.48619878T= , CM000675.1:g.48619878T= GRCh37
NC_000013.9:g.47517879T= NCBI36
NG_047021.1:g.13176T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258662.3:c.438T= MANE Select ENSP00000258662.1:p.Tyr146=
ENST00000258662.2:c.438T= ENSP00000258662.1:p.Tyr146=
NM_018283.2:c.438T= NP_060753.1:p.Tyr146=
NM_018283.3:c.438T= NP_060753.1:p.Tyr146=
NR_136687.1:n.618T=
NR_136688.1:n.618T=
NM_018283.4:c.438T= MANE Select NP_060753.1:p.Tyr146=
NR_136687.2:n.459T=
NR_136688.2:n.459T=