Canonical Allele Identifier: CA483557623
Gene: NUDT15 HGNC NCBI
SUCLA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.48611933A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48037797A>T , CM000675.2:g.48037797A>T GRCh38
NC_000013.10:g.48611933A>T , CM000675.1:g.48611933A>T GRCh37
NC_000013.9:g.47509934A>T NCBI36
NG_047021.1:g.5231A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000258662.3:c.51A>T (NUDT15) MANE Select ENSP00000258662.1:p.Gly17=
ENST00000643246.1:c.-354T>A (SUCLA2) ENSP00000496235.1:n.-354T>A
ENST00000646804.1:c.-276T>A (SUCLA2) ENSP00000493977.1:n.-276T>A
ENST00000258662.2:c.51A>T (NUDT15) ENSP00000258662.1:p.Gly17=
NM_001304745.1:c.51A>T (NUDT15) NP_001291674.1:p.Gly17=
NM_018283.2:c.51A>T (NUDT15) NP_060753.1:p.Gly17=
NM_018283.3:c.51A>T (NUDT15) NP_060753.1:p.Gly17=
NR_136687.1:n.231A>T (NUDT15)
NR_136688.1:n.231A>T (NUDT15)
NM_018283.4:c.51A>T (NUDT15) MANE Select NP_060753.1:p.Gly17=
NM_001304745.2:c.51A>T (NUDT15) NP_001291674.1:p.Gly17=
NR_136687.2:n.72A>T (NUDT15)
NR_136688.2:n.72A>T (NUDT15)