Canonical Allele Identifier: CA2089833606
Gene: NUDT15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045780A= , CM000675.2:g.48045780A= GRCh38
NC_000013.10:g.48619916A= , CM000675.1:g.48619916A= GRCh37
NC_000013.9:g.47517917A= NCBI36
NG_047021.1:g.13214A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258662.3:c.476A= MANE Select ENSP00000258662.1:p.Tyr159=
ENST00000258662.2:c.476A= ENSP00000258662.1:p.Tyr159=
NM_018283.2:c.476A= NP_060753.1:p.Tyr159=
NM_018283.3:c.476A= NP_060753.1:p.Tyr159=
NR_136687.1:n.656A=
NR_136688.1:n.656A=
NM_018283.4:c.476A= MANE Select NP_060753.1:p.Tyr159=
NR_136687.2:n.497A=
NR_136688.2:n.497A=