Canonical Allele Identifier: CA483558092
Gene: NUDT15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.48619899G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48045763G>C , CM000675.2:g.48045763G>C GRCh38
NC_000013.10:g.48619899G>C , CM000675.1:g.48619899G>C GRCh37
NC_000013.9:g.47517900G>C NCBI36
NG_047021.1:g.13197G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258662.3:c.459G>C MANE Select ENSP00000258662.1:p.Leu153=
ENST00000258662.2:c.459G>C ENSP00000258662.1:p.Leu153=
NM_018283.2:c.459G>C NP_060753.1:p.Leu153=
NM_018283.3:c.459G>C NP_060753.1:p.Leu153=
NR_136687.1:n.639G>C
NR_136688.1:n.639G>C
NM_018283.4:c.459G>C MANE Select NP_060753.1:p.Leu153=
NR_136687.2:n.480G>C
NR_136688.2:n.480G>C