Canonical Allele Identifier: CA388154200
Gene: NUDT15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.48619832T>G (hg19) chr13:g.48045696T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045696T>G , CM000675.2:g.48045696T>G GRCh38
NC_000013.10:g.48619832T>G , CM000675.1:g.48619832T>G GRCh37
NC_000013.9:g.47517833T>G NCBI36
NG_047021.1:g.13130T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258662.3:c.392T>G MANE Select ENSP00000258662.1:p.Leu131Arg
ENST00000258662.2:c.392T>G ENSP00000258662.1:p.Leu131Arg
NM_018283.2:c.392T>G NP_060753.1:p.Leu131Arg
NM_018283.3:c.392T>G NP_060753.1:p.Leu131Arg
NR_136687.1:n.572T>G
NR_136688.1:n.572T>G
NM_018283.4:c.392T>G MANE Select NP_060753.1:p.Leu131Arg
NR_136687.2:n.413T>G
NR_136688.2:n.413T>G
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