Canonical Allele Identifier: CA2089833713
Gene: NUDT15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48046028A= , CM000675.2:g.48046028A= GRCh38
NC_000013.10:g.48620164A= , CM000675.1:g.48620164A= GRCh37
NC_000013.9:g.47518165A= NCBI36
NG_047021.1:g.13462A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258662.3:c.*229A= MANE Select ENSP00000258662.1:n.*229A=
ENST00000258662.2:c.*229A= ENSP00000258662.1:n.*229A=
NM_018283.2:c.*229A= NP_060753.1:n.*229A=
NM_018283.3:c.*229A= NP_060753.1:n.*229A=
NR_136687.1:n.718+186A=
NR_136688.1:n.675+229A=
NM_018283.4:c.*229A= MANE Select NP_060753.1:n.*229A=
NR_136687.2:n.559+186A=
NR_136688.2:n.516+229A=
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