Canonical Allele Identifier: CA955771485
Gene: NUDT15 HGNC NCBI

Linked Data

dbSNP Id: rs1950604450
gnomAD v3: 13-48045654-TTC-T
gnomAD v4: 13-48045654-TTC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045656_48045657del , CM000675.2:g.48045656_48045657del GRCh38
NC_000013.10:g.48619792_48619793del , CM000675.1:g.48619792_48619793del GRCh37
NC_000013.9:g.47517793_47517794del NCBI36
NG_047021.1:g.13090_13091del

Transcript Alleles

HGVS Amino-acid change
ENST00000258662.3:c.356-4_356-3del MANE Select ENSP00000258662.1:n.356-4_356-3del
ENST00000258662.2:c.356-4_356-3del ENSP00000258662.1:n.356-4_356-3del
NM_018283.2:c.356-4_356-3del NP_060753.1:n.356-4_356-3del
NM_018283.3:c.356-4_356-3del NP_060753.1:n.356-4_356-3del
NR_136687.1:n.536-4_536-3del
NR_136688.1:n.536-4_536-3del
NM_018283.4:c.356-4_356-3del MANE Select NP_060753.1:n.356-4_356-3del
NR_136687.2:n.377-4_377-3del
NR_136688.2:n.377-4_377-3del
Search 100 bp 5'
Search 100 bp 3'