Canonical Allele Identifier: CA2089829832
Gene: NUDT15 HGNC NCBI
SUCLA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48037792G= , CM000675.2:g.48037792G= GRCh38
NC_000013.10:g.48611928G= , CM000675.1:g.48611928G= GRCh37
NC_000013.9:g.47509929G= NCBI36
NG_047021.1:g.5226G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258662.3:c.46G= (NUDT15) MANE Select ENSP00000258662.1:p.Val16=
ENST00000643246.1:c.-349C= (SUCLA2) ENSP00000496235.1:n.-349C=
ENST00000646804.1:c.-271C= (SUCLA2) ENSP00000493977.1:n.-271C=
ENST00000258662.2:c.46G= (NUDT15) ENSP00000258662.1:p.Val16=
NM_001304745.1:c.46G= (NUDT15) NP_001291674.1:p.Val16=
NM_018283.2:c.46G= (NUDT15) NP_060753.1:p.Val16=
NM_018283.3:c.46G= (NUDT15) NP_060753.1:p.Val16=
NR_136687.1:n.226G= (NUDT15)
NR_136688.1:n.226G= (NUDT15)
NM_018283.4:c.46G= (NUDT15) MANE Select NP_060753.1:p.Val16=
NM_001304745.2:c.46G= (NUDT15) NP_001291674.1:p.Val16=
NR_136687.2:n.67G= (NUDT15)
NR_136688.2:n.67G= (NUDT15)