Canonical Allele Identifier: CA2994942010
Gene: NUDT15 HGNC NCBI
SUCLA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48037782_48037787del , CM000675.2:g.48037782_48037787del GRCh38
NC_000013.10:g.48611918_48611923del , CM000675.1:g.48611918_48611923del GRCh37
NC_000013.9:g.47509919_47509924del NCBI36
NG_047021.1:g.5216_5221del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258662.3:c.36_41del (NUDT15) MANE Select ENSP00000258662.1:p.Gly13_Val14del
ENST00000643246.1:c.-344_-339del (SUCLA2) ENSP00000496235.1:n.-344_-339del
ENST00000646804.1:c.-266_-261del (SUCLA2) ENSP00000493977.1:n.-266_-261del
ENST00000258662.2:c.36_41del (NUDT15) ENSP00000258662.1:p.Gly13_Val14del
NM_001304745.1:c.36_41del (NUDT15) NP_001291674.1:p.Gly13_Val14del
NM_018283.2:c.36_41del (NUDT15) NP_060753.1:p.Gly13_Val14del
NM_018283.3:c.36_41del (NUDT15) NP_060753.1:p.Gly13_Val14del
NR_136687.1:n.216_221del (NUDT15)
NR_136688.1:n.216_221del (NUDT15)
NM_018283.4:c.36_41del (NUDT15) MANE Select NP_060753.1:p.Gly13_Val14del
NM_001304745.2:c.36_41del (NUDT15) NP_001291674.1:p.Gly13_Val14del
NR_136687.2:n.57_62del (NUDT15)
NR_136688.2:n.57_62del (NUDT15)