Canonical Allele Identifier: CA388154069
Gene: NUDT15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.48619802A>C (hg19) chr13:g.48045666A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045666A>C , CM000675.2:g.48045666A>C GRCh38
NC_000013.10:g.48619802A>C , CM000675.1:g.48619802A>C GRCh37
NC_000013.9:g.47517803A>C NCBI36
NG_047021.1:g.13100A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000258662.3:c.362A>C MANE Select ENSP00000258662.1:p.Glu121Ala
ENST00000258662.2:c.362A>C ENSP00000258662.1:p.Glu121Ala
NM_018283.2:c.362A>C NP_060753.1:p.Glu121Ala
NM_018283.3:c.362A>C NP_060753.1:p.Glu121Ala
NR_136687.1:n.542A>C
NR_136688.1:n.542A>C
NM_018283.4:c.362A>C MANE Select NP_060753.1:p.Glu121Ala
NR_136687.2:n.383A>C
NR_136688.2:n.383A>C
Search 100 bp 5'
Search 100 bp 3'