Canonical Allele Identifier: CA609576609

Gene: NUDT15

Linked Data

• dbSNP Id: rs1235254133
• gnomAD v2: 13-48619888-AAAG-A
• gnomAD v4: 13-48045752-AAAG-A
• MyVariant Identifiers: chr13:g.48619889_48619891del (hg19) ; chr13:g.48045753_48045755del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48045757_48045759del , CM000675.2:g.48045757_48045759del	GRCh38
NC_000013.10:g.48619893_48619895del , CM000675.1:g.48619893_48619895del	GRCh37
NC_000013.9:g.47517894_47517896del	NCBI36
NG_047021.1:g.13191_13193del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258662.3:c.453_455del MANE Select	ENSP00000258662.1:p.Glu151del
ENST00000258662.2:c.453_455del	ENSP00000258662.1:p.Glu151del
NM_018283.2:c.453_455del	NP_060753.1:p.Glu151del
NM_018283.3:c.453_455del	NP_060753.1:p.Glu151del
NR_136687.1:n.633_635del
NR_136688.1:n.633_635del
NM_018283.4:c.453_455del MANE Select	NP_060753.1:p.Glu151del
NR_136687.2:n.474_476del
NR_136688.2:n.474_476del