Canonical Allele Identifier: CA2089833714
Gene: NUDT15 HGNC NCBI

Linked Data

dbSNP Id: rs943934716

Genomic Alleles

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

Transcript Alleles

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