Canonical Allele Identifier: CA2089833552
Gene: NUDT15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045661T= , CM000675.2:g.48045661T= GRCh38
NC_000013.10:g.48619797T= , CM000675.1:g.48619797T= GRCh37
NC_000013.9:g.47517798T= NCBI36
NG_047021.1:g.13095T=

Transcript Alleles

HGVS Amino-acid change
ENST00000258662.3:c.357T= MANE Select ENSP00000258662.1:p.Ser119=
ENST00000258662.2:c.357T= ENSP00000258662.1:p.Ser119=
NM_018283.2:c.357T= NP_060753.1:p.Ser119=
NM_018283.3:c.357T= NP_060753.1:p.Ser119=
NR_136687.1:n.537T=
NR_136688.1:n.537T=
NM_018283.4:c.357T= MANE Select NP_060753.1:p.Ser119=
NR_136687.2:n.378T=
NR_136688.2:n.378T=