Canonical Allele Identifier: CA2089829834
Gene: NUDT15 HGNC NCBI
SUCLA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48037794C= , CM000675.2:g.48037794C= GRCh38
NC_000013.10:g.48611930C= , CM000675.1:g.48611930C= GRCh37
NC_000013.9:g.47509931C= NCBI36
NG_047021.1:g.5228C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258662.3:c.48C= (NUDT15) MANE Select ENSP00000258662.1:p.Val16=
ENST00000643246.1:c.-351G= (SUCLA2) ENSP00000496235.1:n.-351G=
ENST00000646804.1:c.-273G= (SUCLA2) ENSP00000493977.1:n.-273G=
ENST00000258662.2:c.48C= (NUDT15) ENSP00000258662.1:p.Val16=
NM_001304745.1:c.48C= (NUDT15) NP_001291674.1:p.Val16=
NM_018283.2:c.48C= (NUDT15) NP_060753.1:p.Val16=
NM_018283.3:c.48C= (NUDT15) NP_060753.1:p.Val16=
NR_136687.1:n.228C= (NUDT15)
NR_136688.1:n.228C= (NUDT15)
NM_018283.4:c.48C= (NUDT15) MANE Select NP_060753.1:p.Val16=
NM_001304745.2:c.48C= (NUDT15) NP_001291674.1:p.Val16=
NR_136687.2:n.69C= (NUDT15)
NR_136688.2:n.69C= (NUDT15)