Canonical Allele Identifier: CA483558086
Gene: NUDT15 HGNC NCBI

Linked Data

COSMIC: COSM469479
MyVariant Identifiers: chr13:g.48619890A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045754A>G , CM000675.2:g.48045754A>G GRCh38
NC_000013.10:g.48619890A>G , CM000675.1:g.48619890A>G GRCh37
NC_000013.9:g.47517891A>G NCBI36
NG_047021.1:g.13188A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258662.3:c.450A>G MANE Select ENSP00000258662.1:p.Lys150=
ENST00000258662.2:c.450A>G ENSP00000258662.1:p.Lys150=
NM_018283.2:c.450A>G NP_060753.1:p.Lys150=
NM_018283.3:c.450A>G NP_060753.1:p.Lys150=
NR_136687.1:n.630A>G
NR_136688.1:n.630A>G
NM_018283.4:c.450A>G MANE Select NP_060753.1:p.Lys150=
NR_136687.2:n.471A>G
NR_136688.2:n.471A>G