Canonical Allele Identifier: CA388154078
Gene: NUDT15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.48619803G>T (hg19) chr13:g.48045667G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045667G>T , CM000675.2:g.48045667G>T GRCh38
NC_000013.10:g.48619803G>T , CM000675.1:g.48619803G>T GRCh37
NC_000013.9:g.47517804G>T NCBI36
NG_047021.1:g.13101G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000258662.3:c.363G>T MANE Select ENSP00000258662.1:p.Glu121Asp
ENST00000258662.2:c.363G>T ENSP00000258662.1:p.Glu121Asp
NM_018283.2:c.363G>T NP_060753.1:p.Glu121Asp
NM_018283.3:c.363G>T NP_060753.1:p.Glu121Asp
NR_136687.1:n.543G>T
NR_136688.1:n.543G>T
NM_018283.4:c.363G>T MANE Select NP_060753.1:p.Glu121Asp
NR_136687.2:n.384G>T
NR_136688.2:n.384G>T
Search 100 bp 5'
Search 100 bp 3'