Canonical Allele Identifier: CA2089833529

Gene: NUDT15

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48045610_48045612delinsCTT , CM000675.2:g.48045610_48045612delinsCTT	GRCh38
NC_000013.10:g.48619746_48619748delinsCTT , CM000675.1:g.48619746_48619748delinsCTT	GRCh37
NC_000013.9:g.47517747_47517749delinsCTT	NCBI36
NG_047021.1:g.13044_13046delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258662.3:c.356-50_356-48delinsCTT MANE Select	ENSP00000258662.1:n.356-50_356-48delinsCTT
ENST00000258662.2:c.356-50_356-48delinsCTT	ENSP00000258662.1:n.356-50_356-48delinsCTT
NM_018283.2:c.356-50_356-48delinsCTT	NP_060753.1:n.356-50_356-48delinsCTT
NM_018283.3:c.356-50_356-48delinsCTT	NP_060753.1:n.356-50_356-48delinsCTT
NR_136687.1:n.536-50_536-48delinsCTT
NR_136688.1:n.536-50_536-48delinsCTT
NM_018283.4:c.356-50_356-48delinsCTT MANE Select	NP_060753.1:n.356-50_356-48delinsCTT
NR_136687.2:n.377-50_377-48delinsCTT
NR_136688.2:n.377-50_377-48delinsCTT