Canonical Allele Identifier: CA2089833672
Gene: NUDT15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045940T= , CM000675.2:g.48045940T= GRCh38
NC_000013.10:g.48620076T= , CM000675.1:g.48620076T= GRCh37
NC_000013.9:g.47518077T= NCBI36
NG_047021.1:g.13374T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258662.3:c.*141T= MANE Select ENSP00000258662.1:n.*141T=
ENST00000258662.2:c.*141T= ENSP00000258662.1:n.*141T=
NM_018283.2:c.*141T= NP_060753.1:n.*141T=
NM_018283.3:c.*141T= NP_060753.1:n.*141T=
NR_136687.1:n.718+98T=
NR_136688.1:n.675+141T=
NM_018283.4:c.*141T= MANE Select NP_060753.1:n.*141T=
NR_136687.2:n.559+98T=
NR_136688.2:n.516+141T=