Canonical Allele Identifier: CA698626159
Gene: NUDT15 HGNC NCBI

Linked Data

dbSNP Id: rs1198076469
gnomAD v4: 13-48045519-C-CAAAGG
MyVariant Identifiers: chr13:g.48619655_48619656insAAAGG (hg19) chr13:g.48045519_48045520insAAAGG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045523_48045524insGAAAG , CM000675.2:g.48045523_48045524insGAAAG GRCh38
NC_000013.10:g.48619659_48619660insGAAAG , CM000675.1:g.48619659_48619660insGAAAG GRCh37
NC_000013.9:g.47517660_47517661insGAAAG NCBI36
NG_047021.1:g.12957_12958insGAAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000258662.3:c.356-137_356-136insGAAAG MANE Select ENSP00000258662.1:n.356-137_356-136insGAA...
ENST00000258662.2:c.356-137_356-136insGAAAG ENSP00000258662.1:n.356-137_356-136insGAA...
NM_018283.2:c.356-137_356-136insGAAAG NP_060753.1:n.356-137_356-136insGAAAG
NM_018283.3:c.356-137_356-136insGAAAG NP_060753.1:n.356-137_356-136insGAAAG
NR_136687.1:n.536-137_536-136insGAAAG
NR_136688.1:n.536-137_536-136insGAAAG
NM_018283.4:c.356-137_356-136insGAAAG MANE Select NP_060753.1:n.356-137_356-136insGAAAG
NR_136687.2:n.377-137_377-136insGAAAG
NR_136688.2:n.377-137_377-136insGAAAG
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