Canonical Allele Identifier: CA6978311
Gene: NUDT15 HGNC NCBI

Linked Data

dbSNP Id: rs747897258

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045651_48045654del , CM000675.2:g.48045651_48045654del GRCh38
NC_000013.10:g.48619787_48619790del , CM000675.1:g.48619787_48619790del GRCh37
NC_000013.9:g.47517788_47517791del NCBI36
NG_047021.1:g.13085_13088del

Transcript Alleles

HGVS Amino-acid change
ENST00000258662.3:c.356-9_356-6del MANE Select ENSP00000258662.1:n.356-9_356-6del
ENST00000258662.2:c.356-9_356-6del ENSP00000258662.1:n.356-9_356-6del
NM_018283.2:c.356-9_356-6del NP_060753.1:n.356-9_356-6del
NM_018283.3:c.356-9_356-6del NP_060753.1:n.356-9_356-6del
NR_136687.1:n.536-9_536-6del
NR_136688.1:n.536-9_536-6del
NM_018283.4:c.356-9_356-6del MANE Select NP_060753.1:n.356-9_356-6del
NR_136687.2:n.377-9_377-6del
NR_136688.2:n.377-9_377-6del