Canonical Allele Identifier: CA388149861

Gene: NUDT15 SUCLA2

Linked Data

• MyVariant Identifiers: chr13:g.48611925G>C (hg19) ; chr13:g.48037789G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48037789G>C , CM000675.2:g.48037789G>C	GRCh38
NC_000013.10:g.48611925G>C , CM000675.1:g.48611925G>C	GRCh37
NC_000013.9:g.47509926G>C	NCBI36
NG_047021.1:g.5223G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000258662.3:c.43G>C (NUDT15) MANE Select	ENSP00000258662.1:p.Gly15Arg
ENST00000643246.1:c.-346C>G (SUCLA2)	ENSP00000496235.1:n.-346C>G
ENST00000646804.1:c.-268C>G (SUCLA2)	ENSP00000493977.1:n.-268C>G
ENST00000258662.2:c.43G>C (NUDT15)	ENSP00000258662.1:p.Gly15Arg
NM_001304745.1:c.43G>C (NUDT15)	NP_001291674.1:p.Gly15Arg
NM_018283.2:c.43G>C (NUDT15)	NP_060753.1:p.Gly15Arg
NM_018283.3:c.43G>C (NUDT15)	NP_060753.1:p.Gly15Arg
NR_136687.1:n.223G>C (NUDT15)
NR_136688.1:n.223G>C (NUDT15)
NM_018283.4:c.43G>C (NUDT15) MANE Select	NP_060753.1:p.Gly15Arg
NM_001304745.2:c.43G>C (NUDT15)	NP_001291674.1:p.Gly15Arg
NR_136687.2:n.64G>C (NUDT15)
NR_136688.2:n.64G>C (NUDT15)