Canonical Allele Identifier: CA2089833569
Gene: NUDT15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045710T= , CM000675.2:g.48045710T= GRCh38
NC_000013.10:g.48619846T= , CM000675.1:g.48619846T= GRCh37
NC_000013.9:g.47517847T= NCBI36
NG_047021.1:g.13144T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258662.3:c.406T= MANE Select ENSP00000258662.1:p.Trp136=
ENST00000258662.2:c.406T= ENSP00000258662.1:p.Trp136=
NM_018283.2:c.406T= NP_060753.1:p.Trp136=
NM_018283.3:c.406T= NP_060753.1:p.Trp136=
NR_136687.1:n.586T=
NR_136688.1:n.586T=
NM_018283.4:c.406T= MANE Select NP_060753.1:p.Trp136=
NR_136687.2:n.427T=
NR_136688.2:n.427T=