Canonical Allele Identifier: CA388149859

Gene: NUDT15 SUCLA2

Linked Data

• dbSNP Id: rs1428135695
• MyVariant Identifiers: chr13:g.48611923T>G (hg19) ; chr13:g.48037787T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48037787T>G , CM000675.2:g.48037787T>G	GRCh38
NC_000013.10:g.48611923T>G , CM000675.1:g.48611923T>G	GRCh37
NC_000013.9:g.47509924T>G	NCBI36
NG_047021.1:g.5221T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258662.3:c.41T>G (NUDT15) MANE Select	ENSP00000258662.1:p.Val14Gly
ENST00000643246.1:c.-344A>C (SUCLA2)	ENSP00000496235.1:n.-344A>C
ENST00000646804.1:c.-266A>C (SUCLA2)	ENSP00000493977.1:n.-266A>C
ENST00000258662.2:c.41T>G (NUDT15)	ENSP00000258662.1:p.Val14Gly
NM_001304745.1:c.41T>G (NUDT15)	NP_001291674.1:p.Val14Gly
NM_018283.2:c.41T>G (NUDT15)	NP_060753.1:p.Val14Gly
NM_018283.3:c.41T>G (NUDT15)	NP_060753.1:p.Val14Gly
NR_136687.1:n.221T>G (NUDT15)
NR_136688.1:n.221T>G (NUDT15)
NM_018283.4:c.41T>G (NUDT15) MANE Select	NP_060753.1:p.Val14Gly
NM_001304745.2:c.41T>G (NUDT15)	NP_001291674.1:p.Val14Gly
NR_136687.2:n.62T>G (NUDT15)
NR_136688.2:n.62T>G (NUDT15)