Canonical Allele Identifier: CA2089833652
Gene: NUDT15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045865G= , CM000675.2:g.48045865G= GRCh38
NC_000013.10:g.48620001G= , CM000675.1:g.48620001G= GRCh37
NC_000013.9:g.47518002G= NCBI36
NG_047021.1:g.13299G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258662.3:c.*66G= MANE Select ENSP00000258662.1:n.*66G=
ENST00000258662.2:c.*66G= ENSP00000258662.1:n.*66G=
NM_018283.2:c.*66G= NP_060753.1:n.*66G=
NM_018283.3:c.*66G= NP_060753.1:n.*66G=
NR_136687.1:n.718+23G=
NR_136688.1:n.675+66G=
NM_018283.4:c.*66G= MANE Select NP_060753.1:n.*66G=
NR_136687.2:n.559+23G=
NR_136688.2:n.516+66G=
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