Canonical Allele Identifier: CA2089833711
Gene: NUDT15 HGNC NCBI

Linked Data

dbSNP Id: rs1593530054
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48046020T>C , CM000675.2:g.48046020T>C GRCh38
NC_000013.10:g.48620156T>C , CM000675.1:g.48620156T>C GRCh37
NC_000013.9:g.47518157T>C NCBI36
NG_047021.1:g.13454T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258662.3:c.*221T>C MANE Select ENSP00000258662.1:n.*221T>C
ENST00000258662.2:c.*221T>C ENSP00000258662.1:n.*221T>C
NM_018283.2:c.*221T>C NP_060753.1:n.*221T>C
NM_018283.3:c.*221T>C NP_060753.1:n.*221T>C
NR_136687.1:n.718+178T>C
NR_136688.1:n.675+221T>C
NM_018283.4:c.*221T>C MANE Select NP_060753.1:n.*221T>C
NR_136687.2:n.559+178T>C
NR_136688.2:n.516+221T>C
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