Canonical Allele Identifier: CA483558010

Gene: NUDT15

Linked Data

• MyVariant Identifiers: chr13:g.48619830C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48045694C>G , CM000675.2:g.48045694C>G	GRCh38
NC_000013.10:g.48619830C>G , CM000675.1:g.48619830C>G	GRCh37
NC_000013.9:g.47517831C>G	NCBI36
NG_047021.1:g.13128C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258662.3:c.390C>G MANE Select	ENSP00000258662.1:p.Pro130=
ENST00000258662.2:c.390C>G	ENSP00000258662.1:p.Pro130=
NM_018283.2:c.390C>G	NP_060753.1:p.Pro130=
NM_018283.3:c.390C>G	NP_060753.1:p.Pro130=
NR_136687.1:n.570C>G
NR_136688.1:n.570C>G
NM_018283.4:c.390C>G MANE Select	NP_060753.1:p.Pro130=
NR_136687.2:n.411C>G
NR_136688.2:n.411C>G