Canonical Allele Identifier: CA388154235
Gene: NUDT15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.48619840C>A (hg19) chr13:g.48045704C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045704C>A , CM000675.2:g.48045704C>A GRCh38
NC_000013.10:g.48619840C>A , CM000675.1:g.48619840C>A GRCh37
NC_000013.9:g.47517841C>A NCBI36
NG_047021.1:g.13138C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258662.3:c.400C>A MANE Select ENSP00000258662.1:p.Leu134Ile
ENST00000258662.2:c.400C>A ENSP00000258662.1:p.Leu134Ile
NM_018283.2:c.400C>A NP_060753.1:p.Leu134Ile
NM_018283.3:c.400C>A NP_060753.1:p.Leu134Ile
NR_136687.1:n.580C>A
NR_136688.1:n.580C>A
NM_018283.4:c.400C>A MANE Select NP_060753.1:p.Leu134Ile
NR_136687.2:n.421C>A
NR_136688.2:n.421C>A
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