Canonical Allele Identifier: CA1620414913

Gene: RPS10-NUDT3 NUDT3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.34335085_34335087delinsCCA , CM000668.2:g.34335085_34335087delinsCCA	GRCh38
NC_000006.11:g.34302862_34302864delinsCCA , CM000668.1:g.34302862_34302864delinsCCA	GRCh37
NC_000006.10:g.34410840_34410842delinsCCA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000605528.2:c.384-39402_384-39400delinsTGG (RPS10-NUDT3)
ENST00000607016.2:c.210+6775_210+6777delinsTGG (NUDT3) MANE Select	ENSP00000476119.1:n.210+6775_210+6777delinsTGG
ENST00000639725.1:c.567+6775_567+6777delinsTGG (RPS10-NUDT3)	ENSP00000492441.1:n.567+6775_567+6777delinsTGG
ENST00000639877.1:c.567+6775_567+6777delinsTGG (RPS10-NUDT3)	ENSP00000491891.1:n.567+6775_567+6777delinsTGG
ENST00000605528.1:c.567+6775_567+6777delinsTGG (RPS10-NUDT3)	ENSP00000475027.1:n.567+6775_567+6777delinsTGG
ENST00000607016.1:c.210+6775_210+6777delinsTGG (NUDT3)	ENSP00000476119.1:n.210+6775_210+6777delinsTGG
NM_001202470.2:c.567+6775_567+6777delinsTGG (RPS10-NUDT3)	NP_001189399.1:n.567+6775_567+6777delinsTGG
NM_006703.3:c.210+6775_210+6777delinsTGG (NUDT3)	NP_006694.1:n.210+6775_210+6777delinsTGG
NM_006703.4:c.210+6775_210+6777delinsTGG (NUDT3) MANE Select	NP_006694.1:n.210+6775_210+6777delinsTGG
NM_001202470.3:c.567+6775_567+6777delinsTGG (RPS10-NUDT3)	NP_001189399.1:n.567+6775_567+6777delinsTGG