Canonical Allele Identifier: CA388154093
Gene: NUDT15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.48619806G>A (hg19) chr13:g.48045670G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045670G>A , CM000675.2:g.48045670G>A GRCh38
NC_000013.10:g.48619806G>A , CM000675.1:g.48619806G>A GRCh37
NC_000013.9:g.47517807G>A NCBI36
NG_047021.1:g.13104G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000258662.3:c.366G>A MANE Select ENSP00000258662.1:p.Trp122Ter
ENST00000258662.2:c.366G>A ENSP00000258662.1:p.Trp122Ter
NM_018283.2:c.366G>A NP_060753.1:p.Trp122Ter
NM_018283.3:c.366G>A NP_060753.1:p.Trp122Ter
NR_136687.1:n.546G>A
NR_136688.1:n.546G>A
NM_018283.4:c.366G>A MANE Select NP_060753.1:p.Trp122Ter
NR_136687.2:n.387G>A
NR_136688.2:n.387G>A
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