Canonical Allele Identifier: CA388154297
Gene: NUDT15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.48619855C>A (hg19) chr13:g.48045719C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045719C>A , CM000675.2:g.48045719C>A GRCh38
NC_000013.10:g.48619855C>A , CM000675.1:g.48619855C>A GRCh37
NC_000013.9:g.47517856C>A NCBI36
NG_047021.1:g.13153C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258662.3:c.415C>A MANE Select ENSP00000258662.1:p.Arg139Ser
ENST00000258662.2:c.415C>A ENSP00000258662.1:p.Arg139Ser
NM_018283.2:c.415C>A NP_060753.1:p.Arg139Ser
NM_018283.3:c.415C>A NP_060753.1:p.Arg139Ser
NR_136687.1:n.595C>A
NR_136688.1:n.595C>A
NM_018283.4:c.415C>A MANE Select NP_060753.1:p.Arg139Ser
NR_136687.2:n.436C>A
NR_136688.2:n.436C>A
Search 100 bp 5'
Search 100 bp 3'